Explore numerous clinical trials jobs in 82 Clinical Trials jobs in London
Director/Senior Director, Decentralized Clinical Trials (DCT), Business Development & Strategy, E...
London, London
IQVIA
Posted 13 days ago
Job Viewed
Job Description
**Join us on our exciting journey!**
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
**Director/Senior Director, Decentralized Clinical Trials (DCT), Business Development & Strategy, EMEA.**
**1 year contract.**
IQVIA's Decentralized Clinical Trials (DCT) enables remote and hybrid clinical studies by connecting patients through digital tools, wearable devices, and virtual visits. It improves accessibility, speeds up recruitment, and ensures compliance across diverse global regulations.
**Responsibilities**
**Client engagement and understanding of client business.**
+ Captures market share by aligning offerings with client needs and regional trends.
+ Maintains and further establishes strong professional relationships across the client organization; with a particular focus on Decentralized Clinical Trials, proactively but appropriately engages with client teams.
+ Responsible for developing and maintaining deep client knowledge; understanding of their business priorities, organizational culture, product portfolio and pipeline, spend/budget priorities.
+ Manages a systematic client-feedback approach, soliciting information from client teams about experience of working with IQVIA.
**Operations management : Leads on the operational management and oversight of IQVIA's DCT activities for local and international markets**
+ Manage assigned strategic and key account relationships individually or in coordination with Global and Regional Sales Teams
+ Identify and respond to customer needs to define potential opportunities for DCT and propose appropriate tailored solutions in line with client needs.
+ Collaborates with IQVIA's Internal RFX, Pricing & Contracts team to support the sales cycle from RFX to sales.
+ Coordinating across clinical operations, technology, and commercial teams to ensure cohesive delivery of DCT solutions.
**Shaping client's perception of IQVIA**
+ Ensures regulatory and operational alignment by tailoring approaches to accommodate Europe's diverse and complex regulatory landscape
+ Identifies opportunities to engage with Client teams to bring relevant marketing and Thought Leadership materials.
+ Manages the annual Strategic Management Review conference.
+ Identifies, or creates opportunities to introduce relevant IQVIANs or teams who are working in areas of high interest for the client, as part of 'peer to peer' engagement (i.e., beyond IQVIA capability presentations, or specific pitches / RFPs)
**Bringing innovation to Client**
+ The Director will champion innovation, integrating emerging technologies and methodologies to differentiate IQVIA services
+ Building on their knowledge of client priorities and in close partnership with the Clinical, Technology Business Partners, and Global Account Director identifies strategic discussions and major opportunities for IQVIA.
+ Actively engages in the Sales and Account Management community, bringing in relevant ideas and success stories from other major accounts.
**Requirements**
+ Extensive knowledge of Decentralized Clinical Trials
+ 10+ years of experience of working in a Sales, Sales engineer, Business development or similar position within the pharmaceutical, CRO, Tech, health, life science or other related regulated industry
+ Proven track record of managing mid-level and high-level contacts
+ Strong organizational, planning, project management skills
+ A developing record of customer contacts at the outsourcing, procurement and mid - management level
+ Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business
+ Excellent analytical skills in assessing and interpreting customer business data
+ Ability to maintain demanding timelines
+ Ability to influence others internally and externally
+ Adaptability and flexibility to changing priorities
+ Demonstrated ability to work creatively in a fast-paced environment
+ Exceptional attention to detail and ability to work simultaneously on multiple priorities
+ Ability to work independently and as a team player
+ Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel
+ Excellent oral and written communication skills
+ Ability to establish and maintain effective working relationships with co-workers, managers, and clients
**Why Join?**
Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In Technology, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry.
You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.
We know that meaningful results require not only the right approach but also **the right people** . Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
It's an exciting time to join and reimagine what's possible in healthcare.
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
**Director/Senior Director, Decentralized Clinical Trials (DCT), Business Development & Strategy, EMEA.**
**1 year contract.**
IQVIA's Decentralized Clinical Trials (DCT) enables remote and hybrid clinical studies by connecting patients through digital tools, wearable devices, and virtual visits. It improves accessibility, speeds up recruitment, and ensures compliance across diverse global regulations.
**Responsibilities**
**Client engagement and understanding of client business.**
+ Captures market share by aligning offerings with client needs and regional trends.
+ Maintains and further establishes strong professional relationships across the client organization; with a particular focus on Decentralized Clinical Trials, proactively but appropriately engages with client teams.
+ Responsible for developing and maintaining deep client knowledge; understanding of their business priorities, organizational culture, product portfolio and pipeline, spend/budget priorities.
+ Manages a systematic client-feedback approach, soliciting information from client teams about experience of working with IQVIA.
**Operations management : Leads on the operational management and oversight of IQVIA's DCT activities for local and international markets**
+ Manage assigned strategic and key account relationships individually or in coordination with Global and Regional Sales Teams
+ Identify and respond to customer needs to define potential opportunities for DCT and propose appropriate tailored solutions in line with client needs.
+ Collaborates with IQVIA's Internal RFX, Pricing & Contracts team to support the sales cycle from RFX to sales.
+ Coordinating across clinical operations, technology, and commercial teams to ensure cohesive delivery of DCT solutions.
**Shaping client's perception of IQVIA**
+ Ensures regulatory and operational alignment by tailoring approaches to accommodate Europe's diverse and complex regulatory landscape
+ Identifies opportunities to engage with Client teams to bring relevant marketing and Thought Leadership materials.
+ Manages the annual Strategic Management Review conference.
+ Identifies, or creates opportunities to introduce relevant IQVIANs or teams who are working in areas of high interest for the client, as part of 'peer to peer' engagement (i.e., beyond IQVIA capability presentations, or specific pitches / RFPs)
**Bringing innovation to Client**
+ The Director will champion innovation, integrating emerging technologies and methodologies to differentiate IQVIA services
+ Building on their knowledge of client priorities and in close partnership with the Clinical, Technology Business Partners, and Global Account Director identifies strategic discussions and major opportunities for IQVIA.
+ Actively engages in the Sales and Account Management community, bringing in relevant ideas and success stories from other major accounts.
**Requirements**
+ Extensive knowledge of Decentralized Clinical Trials
+ 10+ years of experience of working in a Sales, Sales engineer, Business development or similar position within the pharmaceutical, CRO, Tech, health, life science or other related regulated industry
+ Proven track record of managing mid-level and high-level contacts
+ Strong organizational, planning, project management skills
+ A developing record of customer contacts at the outsourcing, procurement and mid - management level
+ Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business
+ Excellent analytical skills in assessing and interpreting customer business data
+ Ability to maintain demanding timelines
+ Ability to influence others internally and externally
+ Adaptability and flexibility to changing priorities
+ Demonstrated ability to work creatively in a fast-paced environment
+ Exceptional attention to detail and ability to work simultaneously on multiple priorities
+ Ability to work independently and as a team player
+ Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel
+ Excellent oral and written communication skills
+ Ability to establish and maintain effective working relationships with co-workers, managers, and clients
**Why Join?**
Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In Technology, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry.
You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.
We know that meaningful results require not only the right approach but also **the right people** . Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
It's an exciting time to join and reimagine what's possible in healthcare.
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
0
Senior Clinical Research Associate (CRA) - Oncology Trials
SW1A 0AA London, London
£60000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a global biopharmaceutical company at the forefront of medical innovation, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their dynamic team. This is a remote-based role, offering the flexibility to work from anywhere within the UK, with travel required to study sites as needed. You will play a pivotal role in overseeing the conduct of complex oncology clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. Your responsibilities will include site initiation, monitoring, and close-out visits; evaluating the quality and integrity of trial data; and ensuring patient safety. You will serve as the primary point of contact for assigned investigational sites, building strong relationships with investigators and site staff to facilitate efficient trial progress. This involves verifying source documentation, reviewing case report forms (CRFs), and resolving data queries in a timely manner. You will also be responsible for identifying and escalating potential issues or risks to study management, and contributing to the development of site monitoring plans. Strong communication and collaboration skills are essential for working effectively with internal teams, including clinical operations, data management, and medical affairs, as well as external partners.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, coupled with a minimum of 5 years of progressive experience as a Clinical Research Associate, with a significant portion dedicated to oncology trials. A thorough understanding of ICH-GCP guidelines and relevant regulatory requirements (e.g., FDA, EMA) is mandatory. Proven experience conducting site monitoring visits, including initiation, interim, and close-out activities, is essential. Excellent organizational skills, meticulous attention to detail, and the ability to manage multiple priorities effectively are required. Strong written and verbal communication skills are necessary for clear reporting and effective site communication. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. The ability to travel independently to sites as needed is a must. This remote role offers an exceptional opportunity to contribute to life-saving oncology research from the comfort of your own home, while maintaining a critical link to clinical sites.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, coupled with a minimum of 5 years of progressive experience as a Clinical Research Associate, with a significant portion dedicated to oncology trials. A thorough understanding of ICH-GCP guidelines and relevant regulatory requirements (e.g., FDA, EMA) is mandatory. Proven experience conducting site monitoring visits, including initiation, interim, and close-out activities, is essential. Excellent organizational skills, meticulous attention to detail, and the ability to manage multiple priorities effectively are required. Strong written and verbal communication skills are necessary for clear reporting and effective site communication. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is expected. The ability to travel independently to sites as needed is a must. This remote role offers an exceptional opportunity to contribute to life-saving oncology research from the comfort of your own home, while maintaining a critical link to clinical sites.
This advertiser has chosen not to accept applicants from your region.
1
Biotech Client Partner - Regulatory, Drug Development, Clinical, Consulting and Real-World Strate...
London, London
IQVIA
Posted 13 days ago
Job Viewed
Job Description
**Join us on our exciting journey!**
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
**Biotech** **Client Partner - Regulatory, Drug Development, Clinical, Consulting and Real-World Strategy, EMEA**
**Role Overview**
As a Biotech Client Partner you will support on selected clients from the point of view their asset development and build relationships with C-level stakeholders. The focus will be on the crafting of solutions including (but not limited to) Regulatory and Drug Development strategy, Clinical development, consulting, analytic services, Real World Evidence and elements of Technology.
This role will operate across the client organization, particularly with senior global stakeholders to define and execute our priorities to move the client business forward, providing the conduit between the client and the rest of IQVIA.
This role forms one of the key client roles and should closely partner with the Account Directors from multiple departments including but not limited to Research and Development Solution (RDS), Real World Evidence (RWE), Commercial services, Patient Centric Services, Technology and laboratories to drive the account forward in accordance with both short-term priorities and long-term vision.
This role also requires a close interaction with the project execution team and oversight of the different department involved to consolidate the development of a close relation with the client, facilitating a smooth project delivery and repeat business.
**Responsibilities**
+ Drive overall business growth globally with a focus on increasing sales, revenue, and profitability into the assigned global account and assigned target assets.
+ Support the development of the Clinical, Regulatory and Drug Development Solutions, Real World & Medical Affairs account asset strategy with input from the broader account aligned team and orchestrate the operational execution including selection and planning around assets.
+ Align the account asset strategy with RDS, Regulatory, Drug Development & RWE to ensure a joined up 'Molecule to Market' engagement.
+ Build long term relationships with Executive leaders within the client to ensure long term revenue growth for RDS, Regulatory, Drug Development and RWE
+ Leverage your existing external network to gain referrals and facilitate establishment of a trust with your clients
+ Influence the client's strategy and position IQVIA through thought leadership and innovation aligned to client strategic asset priorities. Leverage senior IQVIA resources and subject matter experts as needed in building preferred supplier relationships.
+ Proactively engage client C-level leaders by anticipating client needs and leveraging the IQVIA cross departmental expertise to develop both short- and long-term cross functional solutions.
**Our Ideal Candidate**
+ Proven expertise across the Biotech, Pharma, and Life Sciences drug development lifecycle-including medical, pre-clinical, clinical operations, and regulatory domains.
+ Strong understanding of Biotech business strategy and operational processes, gained within a professional services environment (CRO).
+ Solid Consulting background with a track record of delivering client-focused solutions.
+ Well-connected within the Biotech ecosystem, with an extensive external network.
+ A natural relationship builder and influencer, able to engage stakeholders across all levels.
+ Skilled in consultative selling, with the ability to uncover client needs and orchestrate cross-functional teams to deliver compelling, tailored solutions.
+ Comfortable engaging with senior executives and navigating complex client environments.
+ Experienced in solution development-able to craft persuasive narratives, generate bold ideas, and back them with evidence.
+ Strong collaboration, influence, and persuasion capabilities.
+ Adept at operating within complex matrix organizations, aligning diverse stakeholders.
+ Demonstrated success in selling and negotiating large-scale, cross-functional solutions.
+ Brings excellent communication, organizational skills, analytical thinking, and problem-solving ability.
**Why Join?**
You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.
We know that meaningful results require not only the right approach but also **the fitting personality** . Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
It is an exciting time to join and reimagine what's possible in healthcare.
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.
**Biotech** **Client Partner - Regulatory, Drug Development, Clinical, Consulting and Real-World Strategy, EMEA**
**Role Overview**
As a Biotech Client Partner you will support on selected clients from the point of view their asset development and build relationships with C-level stakeholders. The focus will be on the crafting of solutions including (but not limited to) Regulatory and Drug Development strategy, Clinical development, consulting, analytic services, Real World Evidence and elements of Technology.
This role will operate across the client organization, particularly with senior global stakeholders to define and execute our priorities to move the client business forward, providing the conduit between the client and the rest of IQVIA.
This role forms one of the key client roles and should closely partner with the Account Directors from multiple departments including but not limited to Research and Development Solution (RDS), Real World Evidence (RWE), Commercial services, Patient Centric Services, Technology and laboratories to drive the account forward in accordance with both short-term priorities and long-term vision.
This role also requires a close interaction with the project execution team and oversight of the different department involved to consolidate the development of a close relation with the client, facilitating a smooth project delivery and repeat business.
**Responsibilities**
+ Drive overall business growth globally with a focus on increasing sales, revenue, and profitability into the assigned global account and assigned target assets.
+ Support the development of the Clinical, Regulatory and Drug Development Solutions, Real World & Medical Affairs account asset strategy with input from the broader account aligned team and orchestrate the operational execution including selection and planning around assets.
+ Align the account asset strategy with RDS, Regulatory, Drug Development & RWE to ensure a joined up 'Molecule to Market' engagement.
+ Build long term relationships with Executive leaders within the client to ensure long term revenue growth for RDS, Regulatory, Drug Development and RWE
+ Leverage your existing external network to gain referrals and facilitate establishment of a trust with your clients
+ Influence the client's strategy and position IQVIA through thought leadership and innovation aligned to client strategic asset priorities. Leverage senior IQVIA resources and subject matter experts as needed in building preferred supplier relationships.
+ Proactively engage client C-level leaders by anticipating client needs and leveraging the IQVIA cross departmental expertise to develop both short- and long-term cross functional solutions.
**Our Ideal Candidate**
+ Proven expertise across the Biotech, Pharma, and Life Sciences drug development lifecycle-including medical, pre-clinical, clinical operations, and regulatory domains.
+ Strong understanding of Biotech business strategy and operational processes, gained within a professional services environment (CRO).
+ Solid Consulting background with a track record of delivering client-focused solutions.
+ Well-connected within the Biotech ecosystem, with an extensive external network.
+ A natural relationship builder and influencer, able to engage stakeholders across all levels.
+ Skilled in consultative selling, with the ability to uncover client needs and orchestrate cross-functional teams to deliver compelling, tailored solutions.
+ Comfortable engaging with senior executives and navigating complex client environments.
+ Experienced in solution development-able to craft persuasive narratives, generate bold ideas, and back them with evidence.
+ Strong collaboration, influence, and persuasion capabilities.
+ Adept at operating within complex matrix organizations, aligning diverse stakeholders.
+ Demonstrated success in selling and negotiating large-scale, cross-functional solutions.
+ Brings excellent communication, organizational skills, analytical thinking, and problem-solving ability.
**Why Join?**
You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.
We know that meaningful results require not only the right approach but also **the fitting personality** . Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
It is an exciting time to join and reimagine what's possible in healthcare.
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
2
Senior Pharmaceutical Research Scientist
SW1A 0AA London, London
£65000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a highly qualified and motivated Senior Pharmaceutical Research Scientist to join their innovative R&D department. This is an exciting, lab-based role where you will contribute to the discovery and development of novel therapeutics. You will be instrumental in designing and executing research projects, analyzing experimental data, and contributing to the advancement of our drug pipeline.
Your responsibilities will include conducting cutting-edge research in areas such as medicinal chemistry, pharmacology, or drug discovery. You will be involved in the design, synthesis, and characterization of potential drug candidates, as well as evaluating their efficacy and safety in preclinical models. Strong skills in experimental design, data interpretation, and troubleshooting are crucial.
The ideal candidate will possess a PhD in Pharmaceutical Sciences, Chemistry, Biology, or a related discipline, coupled with significant post-doctoral or industry experience in drug discovery. Proven expertise in relevant scientific techniques (e.g., cell-based assays, molecular biology, in vivo models) and a deep understanding of pharmacology and medicinal chemistry principles are essential. Experience with analytical techniques such as HPLC, Mass Spectrometry, and NMR is highly desirable.
You will be expected to stay current with scientific literature, identify new research opportunities, and contribute to the intellectual property strategy of the company. Strong written and verbal communication skills are required for preparing research reports, scientific publications, and presentations. The ability to work collaboratively in a multidisciplinary team environment is paramount. You will also mentor junior scientists and contribute to the overall scientific direction of the research group.
This is a fantastic opportunity for an accomplished scientist to make a significant impact in the pharmaceutical industry, working on groundbreaking research and development. Join a dynamic and well-resourced team dedicated to improving patient outcomes through innovative science in London, England, UK .
Your responsibilities will include conducting cutting-edge research in areas such as medicinal chemistry, pharmacology, or drug discovery. You will be involved in the design, synthesis, and characterization of potential drug candidates, as well as evaluating their efficacy and safety in preclinical models. Strong skills in experimental design, data interpretation, and troubleshooting are crucial.
The ideal candidate will possess a PhD in Pharmaceutical Sciences, Chemistry, Biology, or a related discipline, coupled with significant post-doctoral or industry experience in drug discovery. Proven expertise in relevant scientific techniques (e.g., cell-based assays, molecular biology, in vivo models) and a deep understanding of pharmacology and medicinal chemistry principles are essential. Experience with analytical techniques such as HPLC, Mass Spectrometry, and NMR is highly desirable.
You will be expected to stay current with scientific literature, identify new research opportunities, and contribute to the intellectual property strategy of the company. Strong written and verbal communication skills are required for preparing research reports, scientific publications, and presentations. The ability to work collaboratively in a multidisciplinary team environment is paramount. You will also mentor junior scientists and contribute to the overall scientific direction of the research group.
This is a fantastic opportunity for an accomplished scientist to make a significant impact in the pharmaceutical industry, working on groundbreaking research and development. Join a dynamic and well-resourced team dedicated to improving patient outcomes through innovative science in London, England, UK .
This advertiser has chosen not to accept applicants from your region.
3
Senior Pharmaceutical Research Scientist
SW1A 0AA London, London
£70000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a globally recognized pharmaceutical company at the forefront of drug discovery and development, is seeking a highly skilled Senior Pharmaceutical Research Scientist to join their innovative research division based in **London, England, UK**. This pivotal role involves designing and executing complex research projects aimed at identifying novel therapeutic targets and developing groundbreaking treatments for unmet medical needs. The ideal candidate will possess a PhD in Pharmacology, Biochemistry, Molecular Biology, or a closely related discipline, coupled with extensive post-doctoral experience and a proven track record of significant contributions in pharmaceutical R&D. You will be responsible for leading a team of talented scientists, mentoring junior researchers, and managing project timelines and budgets. A deep understanding of disease mechanisms, assay development, drug screening, and preclinical development is essential. Strong analytical skills, a meticulous approach to experimental design and data interpretation, and excellent written and verbal communication skills are required. This hybrid role offers a dynamic research environment with opportunities for both laboratory-based work and strategic planning, fostering collaboration within a world-class scientific community. Experience with specific therapeutic areas such as oncology, immunology, or CNS disorders is highly desirable.
Key Responsibilities:
Key Responsibilities:
- Design, execute, and interpret complex research experiments in drug discovery.
- Lead and mentor a team of research scientists and technicians.
- Develop and validate novel biochemical and cellular assays.
- Conduct high-throughput screening (HTS) campaigns.
- Investigate mechanisms of action for potential drug candidates.
- Analyze and present research findings to internal and external stakeholders.
- Manage project timelines, resources, and budgets effectively.
- Collaborate with cross-functional teams, including chemistry, DMPK, and toxicology.
- Stay abreast of the latest scientific literature and technological advancements.
- Contribute to the preparation of patent applications and scientific publications.
- Ensure compliance with GxP guidelines and laboratory safety standards.
- Identify and evaluate new therapeutic targets and drug development opportunities.
This advertiser has chosen not to accept applicants from your region.
4
Lead Pharmaceutical Research Scientist
WC2N 5DU London, London
£70000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a globally recognised pharmaceutical company, is seeking an exceptional Lead Pharmaceutical Research Scientist to join their cutting-edge R&D department, operating remotely. This vital role will drive innovation and lead critical research projects aimed at discovering and developing novel therapeutic agents. You will be responsible for designing and executing complex research experiments, analysing data, and interpreting results to advance drug discovery pipelines. Key duties include overseeing research methodologies, mentoring junior scientists, and collaborating with cross-functional teams, including medicinal chemistry, pharmacology, and clinical development, in a virtual environment. The Lead Pharmaceutical Research Scientist will contribute significantly to scientific publications, patent applications, and regulatory submissions. The ideal candidate will possess a PhD in Pharmacology, Biochemistry, Molecular Biology, or a closely related life science discipline, with a strong publication record and demonstrated experience in leading research projects. Expertise in specific therapeutic areas or drug development technologies is highly advantageous. Exceptional analytical, critical thinking, and problem-solving skills are essential. Strong leadership capabilities, excellent written and verbal communication skills, and the ability to effectively manage research timelines and budgets are paramount. We are looking for a highly motivated and scientifically driven individual with a passion for translating scientific discoveries into life-changing medicines. This is a remote position offering immense professional growth opportunities and the chance to contribute to groundbreaking pharmaceutical research at the forefront of medical innovation. You will work with a world-class team dedicated to improving global health outcomes through scientific excellence and collaboration.
This advertiser has chosen not to accept applicants from your region.
5
Lead Pharmaceutical Research Scientist
SW1A 0AA London, London
£75000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a renowned global pharmaceutical company, is seeking a highly motivated and experienced Lead Pharmaceutical Research Scientist to join their innovative drug discovery team in London, England, UK . This critical role involves leading a team of scientists in the identification, validation, and optimization of novel drug targets and therapeutic candidates. You will be instrumental in designing and executing complex research projects, interpreting data, and contributing to the strategic direction of the company's R&D pipeline. This is a hybrid role, offering a blend of laboratory-based work and strategic planning conducted remotely.
Key Responsibilities:
Key Responsibilities:
- Lead and mentor a team of research associates and scientists in a cutting-edge drug discovery laboratory.
- Design, develop, and implement experimental strategies to identify and validate novel therapeutic targets across various disease areas.
- Oversee the execution of complex research projects, ensuring timely and high-quality data generation.
- Analyze and interpret experimental data, drawing robust conclusions and making informed recommendations for project progression.
- Contribute to the strategic planning and prioritization of drug discovery projects within the R&D pipeline.
- Develop and maintain strong collaborative relationships with internal teams (e.g., DMPK, CMC, Clinical) and external partners (academic institutions, CROs).
- Prepare and present research findings at internal meetings, scientific conferences, and in peer-reviewed publications.
- Ensure compliance with all laboratory safety regulations, ethical guidelines, and company policies.
- Contribute to the development of intellectual property through invention disclosures and patent applications.
- Manage research budgets and resources effectively.
- Stay abreast of the latest scientific literature, technological advancements, and competitive landscape in pharmaceutical R&D.
- Assist in the recruitment and training of new research personnel.
- Ph.D. in Molecular Biology, Pharmacology, Biochemistry, or a related life science discipline.
- A minimum of 7 years of post-doctoral research experience in the pharmaceutical or biotechnology industry, with a significant focus on drug discovery.
- Proven experience in leading and managing scientific teams and projects.
- Demonstrated expertise in target identification and validation, assay development, and lead optimization.
- Strong understanding of key therapeutic areas (e.g., oncology, immunology, CNS).
- Hands-on experience with relevant laboratory techniques and instrumentation.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional written and verbal communication skills, including experience in presenting complex scientific data.
- A strong publication record and/or patent filings.
- Ability to work effectively in a collaborative, fast-paced, and dynamic research environment.
- Experience with hybrid work models and remote collaboration tools is desirable.
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6
Senior Pharmaceutical Research Scientist
WC1A 0AA London, London
£60000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking an exceptional Senior Pharmaceutical Research Scientist to join their state-of-the-art laboratories in London, England, UK . This is a critical, hands-on role focused on the discovery and development of novel therapeutic agents. You will lead and contribute to complex research projects, from target identification and validation through to preclinical candidate selection. Your responsibilities will include designing and executing sophisticated in vitro and in vivo experiments, analyzing biological data, and interpreting results to guide research strategies. You will be expected to stay abreast of the latest scientific literature and technological advancements in relevant therapeutic areas, such as oncology, immunology, or infectious diseases. The ideal candidate will have a proven track record in drug discovery, with extensive experience in molecular biology, cell biology, biochemistry, or pharmacology. Proficiency in various experimental techniques, including cell culture, immunoassays (ELISA, Western blotting), flow cytometry, and genetic manipulation (CRISPR, siRNA), is essential. You will also be responsible for mentoring junior scientists, contributing to the preparation of research reports, scientific publications, and patent applications, and presenting findings at internal and external scientific meetings. Collaboration with internal teams (e.g., DMPK, toxicology, clinical development) and external partners will be a key aspect of this role. A PhD in a relevant life science discipline, coupled with at least 5 years of post-doctoral or industry research experience, is required. Strong analytical and problem-solving skills, excellent written and verbal communication abilities, and a commitment to scientific rigor are paramount. This is a unique opportunity to make a significant impact on the development of life-saving medicines within a highly collaborative and intellectually stimulating environment.
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7
Principal Pharmaceutical Research Scientist
SW1A 0AA London, London
£80000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client is seeking a highly accomplished Principal Pharmaceutical Research Scientist to lead groundbreaking research initiatives within their state-of-the-art laboratories in London, England, UK . This senior role is critical for driving innovation in drug discovery and development, focusing on novel therapeutic agents and advanced pharmaceutical technologies. The successful candidate will possess deep expertise in a specific area of pharmaceutical research (e.g., oncology, immunology, neuroscience) and a proven track record of successfully bringing early-stage research projects to fruition. You will be responsible for designing and executing complex experiments, interpreting data, and making critical decisions that guide research strategy.
Key responsibilities include leading a team of talented scientists, mentoring junior researchers, and fostering a collaborative and intellectually stimulating research environment. You will manage research projects from ideation through to preclinical development, ensuring alignment with company objectives and timelines. This involves extensive literature review, hypothesis generation, experimental design, and rigorous data analysis. The Principal Scientist will be expected to present findings at scientific conferences, publish in peer-reviewed journals, and contribute to the intellectual property portfolio of the company. Collaboration with internal departments (e.g., CMC, Regulatory Affairs) and external academic institutions or partners will be essential. This hybrid role requires a significant presence in the lab for hands-on research and team leadership, with opportunities for remote work for data analysis and report writing.
Key Responsibilities:
Qualifications:
Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
Minimum of 10 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
Demonstrated leadership experience managing research teams and projects.
In-depth knowledge and hands-on expertise in a specific therapeutic area.
Proven track record of scientific innovation, publications, and patents.
Extensive experience with drug discovery and preclinical development processes.
Excellent analytical, problem-solving, and critical thinking skills.
Strong written and verbal communication and presentation abilities.
Ability to work effectively in a collaborative, fast-paced environment.
Key responsibilities include leading a team of talented scientists, mentoring junior researchers, and fostering a collaborative and intellectually stimulating research environment. You will manage research projects from ideation through to preclinical development, ensuring alignment with company objectives and timelines. This involves extensive literature review, hypothesis generation, experimental design, and rigorous data analysis. The Principal Scientist will be expected to present findings at scientific conferences, publish in peer-reviewed journals, and contribute to the intellectual property portfolio of the company. Collaboration with internal departments (e.g., CMC, Regulatory Affairs) and external academic institutions or partners will be essential. This hybrid role requires a significant presence in the lab for hands-on research and team leadership, with opportunities for remote work for data analysis and report writing.
Key Responsibilities:
- Lead and direct pharmaceutical research projects in a specialized therapeutic area.
- Design and execute complex in vitro and in vivo experimental studies.
- Develop and validate novel assays and methodologies.
- Analyze and interpret scientific data to drive research decisions.
- Mentor and manage a team of research scientists and technicians.
- Contribute to the strategic planning of the research pipeline.
- Prepare research reports, publications, and patent applications.
- Collaborate effectively with cross-functional teams and external partners.
- Stay at the forefront of scientific advancements in pharmaceutical research.
- Ensure compliance with laboratory safety protocols and ethical guidelines.
Qualifications:
Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
Minimum of 10 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
Demonstrated leadership experience managing research teams and projects.
In-depth knowledge and hands-on expertise in a specific therapeutic area.
Proven track record of scientific innovation, publications, and patents.
Extensive experience with drug discovery and preclinical development processes.
Excellent analytical, problem-solving, and critical thinking skills.
Strong written and verbal communication and presentation abilities.
Ability to work effectively in a collaborative, fast-paced environment.
This advertiser has chosen not to accept applicants from your region.
8
Senior Pharmaceutical Research Scientist
WC1X 0AA London, London
£75000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client is actively seeking a highly qualified and accomplished Senior Pharmaceutical Research Scientist to join their pioneering, fully remote R&D department. This role is crucial for driving innovation in drug discovery and development, supporting projects aimed at addressing critical health needs for clients worldwide, including those based in London, England, UK . The Senior Pharmaceutical Research Scientist will lead research initiatives, design and execute complex experiments, and analyse data to advance our understanding of disease mechanisms and identify novel therapeutic targets. You will be responsible for planning and managing research projects, ensuring adherence to strict scientific protocols, and contributing to the preparation of research reports and publications. Key responsibilities include developing and validating new assays, optimising experimental conditions, and interpreting complex biological data. Experience with various molecular biology techniques, cell culture, high-throughput screening, and data analysis software is essential. A deep understanding of drug development processes, regulatory requirements, and intellectual property considerations is highly valued. The successful candidate will possess excellent leadership and mentorship skills, with the ability to guide junior researchers and foster a collaborative research environment. This fully remote position demands exceptional scientific rigor, critical thinking, and a proactive approach to problem-solving. The ideal candidate will have a strong publication record and a proven track record in the pharmaceutical or biotechnology industry. Join our dedicated team of scientists and contribute to groundbreaking advancements in pharmaceutical research.
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