96 Clinical Trials jobs in London

Clinical Trials Pharmacist

Chelsea, London NHS

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The trials team is expanding, and we have a fantastic opportunity for a passionate, motivated, and dynamic pharmacist to join the Pharmacy Clinical Trials team at The Royal Marsden (RMH) NHS Foundation Trust.

An exciting time to join our service, focussing on delivering high-quality care to patients and staff. The RMH is a world-leading cancer centre with sites in Chelsea and Sutton, plus a Medical Day Care Unit at Kingston Hospital.

Prior clinical trials experience; oncology or haemato-oncology knowledge is an advantage. Working alongside pharmacists, technicians, and assistants as part of a Multi-Disciplinary Team committed to delivering outstanding patient care.

Our team supports the research strategy of "taking personalized cancer treatment to the next level," with approximately 380 active IMP studies and increasingly complex new clinical trials across all specialties, including gene therapies and cellular therapies studies.

The RMH, in association with its partner, The ICR, has an unparalleled global reputation for patient care, research, and education. Through our partnership, we pioneer new cancer therapies through complex transitional studies and Phase I-III clinical trials, making us one of

Europe's largest comprehensive cancer centres.

The hospital has recently introduced the EPIC digital health record system, and we are looking to use the full capabilities of this system to support the pharmacy teams and become a more efficient and truly paperless.

  • To contribute to the provision of the pharmacy clinical trials service to the Dispensaries (Chelsea & Sutton), Medical day Unit, West Wing Clinical Research Centre (WWCRC), Oak ward and day case areas of the Drug Development Unit and the Clinical Trial Dispensary across both sites.
  • To assist the Clinical Trials Team with any day-to day clinical, dispensing, ward and research day units' queries.
  • To provide clinical trials advice while covering the research clinics and attending MDT.
  • To support research clinic prescribing
  • Provide clinical trial support and advice to other areas within pharmacy e.g. aseptic service, clinical services and to the research teams.
  • To support the clinical trial team with clinical trial set-up of new studies, revision of amendments for ongoing studies already open at the trust, to provide continued support for the running and maintenance of current trial activity.
  • To contribute to the provision of the pharmacy clinical trials service to the individual clinical units, R&D and the Trust.

The RMH NHS Foundation Trust is a world-leading cancer centre, offering patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Day-care Unit in Kingston Hospital

At RMH, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.

At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits and learning and development opportunities.

We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements. A variety of other staff benefits including employee assistance programme, discounted gym membership, onsite fitness classes, car schemes.

For further information on this role, please see the attached detailed Job Description and Person Specification:

Ensure that clinical trial services policies and procedures are adhered to and accreditation records and training documents are completed appropriately.

Promote optimal and appropriate drug use and high quality prescribing practice within the Trust.

To respond appropriately to requests from medical and nursing staff for information and advice about selection and use of drug therapy.

Support the Lead Pharmacist, Clinical R&D and the Chief Technician, Clinical Trials in work towards maintaining quality standards required by Medicines and Health products Regulatory Agency and ensuring principles of Good Clinical Practice are applied at all times.

To support the Lead Pharmacist, Clinical R&D with the Clinical Governance and Risk Management Strategy within the department and throughout the Trust.

Take part in clinical trials audit or any other project work relevant to this post.

Participate in any pharmacy initiatives or working groups as appropriate.

To support the Trial Team in maintaining up to date of Key Performance Indicators for all trail activities.

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Deputy Production Manager (Pharmacy / Clinical Trials / GMP Manufacturing)

Hammersmith, London BioTalent

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Job Description

Job Title: Deputy Production Manager

Company: Leading UK Clinical Research Organisation

Location: London, UK

Working Schedule: Full-time – On-site

Start Date: ASAP


About the Company

This organisation is one of the UK’s leading independent early-phase clinical research centres. They have built a strong reputation for running safe, high-quality Phase I trials with biotech and pharma partners worldwide. The pharmacy and production teams are central to this mission, preparing and managing investigational medicines under strict GMP.


The company is also in an exciting period of expansion . Facility upgrades are already underway, with further improvements due over the next 1–2 years. These will bring new capabilities, enhanced staff benefits, and a modernised GMP environment. Joining now means being part of that journey – shaping processes, influencing standards, and playing a direct role in how the pharmacy function grows.


The Role

We’re looking for a Deputy Production Manager to join the pharmacy team. This is a senior production role, ideal for someone with aseptic training and strong production management experience. You’ll deputise for the Production Manager, lead technicians, and ensure the highest GMP standards across sterile and non-sterile manufacturing.


Key responsibilities include:

  • Leading the day-to-day management of the production team, including rotas and capacity planning.
  • Writing, reviewing, and maintaining SOPs.
  • Overseeing preparation of sterile and non-sterile formulations (suspensions, solutions, capsules).
  • Managing environmental monitoring and aseptic operations.
  • Representing pharmacy during audits and inspections.
  • Mentoring technicians and apprentices, ensuring compliance and quality standards.
  • Supporting the Production Manager with scheduling, documentation, and sponsor liaison.


You’ll work closely with QA and clinical operations, reporting directly into the Principal Pharmacist & Production Manager.


Key Requirements

We’re ideally looking for someone with:

  • A science-based degree (pharmacy, pharmaceutical sciences, microbiology, or similar).
  • Strong GMP knowledge with hands-on aseptic/sterile manufacturing experience.
  • Experience preparing sterile and non-sterile medicines (solutions, suspensions, capsules).
  • Previous supervisory or management experience in a GMP environment.
  • Ability to write, review, and maintain SOPs.
  • Confident with documentation, email communication, and regulatory standards.
  • GPhC registration preferred but not essential if equivalent GMP aseptic production experience can be demonstrated.


What’s on Offer

  • 25 days annual leave, pension, and overtime pay.
  • A collaborative, supportive environment with fast feedback and interview turnaround.
  • The chance to play a visible, high-responsibility role in shaping early-phase clinical research.
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Deputy Production Manager (Pharmacy / Clinical Trials / GMP Manufacturing)

Hammersmith, London BioTalent

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Job Description

Job Description

Job Title: Deputy Production Manager

Company: Leading UK Clinical Research Organisation

Location: London, UK

Working Schedule: Full-time – On-site

Start Date: ASAP


About the Company

This organisation is one of the UK’s leading independent early-phase clinical research centres. They have built a strong reputation for running safe, high-quality Phase I trials with biotech and pharma partners worldwide. The pharmacy and production teams are central to this mission, preparing and managing investigational medicines under strict GMP.


The company is also in an exciting period of expansion . Facility upgrades are already underway, with further improvements due over the next 1–2 years. These will bring new capabilities, enhanced staff benefits, and a modernised GMP environment. Joining now means being part of that journey – shaping processes, influencing standards, and playing a direct role in how the pharmacy function grows.


The Role

We’re looking for a Deputy Production Manager to join the pharmacy team. This is a senior production role, ideal for someone with aseptic training and strong production management experience. You’ll deputise for the Production Manager, lead technicians, and ensure the highest GMP standards across sterile and non-sterile manufacturing.


Key responsibilities include:

  • Leading the day-to-day management of the production team, including rotas and capacity planning.
  • Writing, reviewing, and maintaining SOPs.
  • Overseeing preparation of sterile and non-sterile formulations (suspensions, solutions, capsules).
  • Managing environmental monitoring and aseptic operations.
  • Representing pharmacy during audits and inspections.
  • Mentoring technicians and apprentices, ensuring compliance and quality standards.
  • Supporting the Production Manager with scheduling, documentation, and sponsor liaison.


You’ll work closely with QA and clinical operations, reporting directly into the Principal Pharmacist & Production Manager.


Key Requirements

We’re ideally looking for someone with:

  • A science-based degree (pharmacy, pharmaceutical sciences, microbiology, or similar).
  • Strong GMP knowledge with hands-on aseptic/sterile manufacturing experience.
  • Experience preparing sterile and non-sterile medicines (solutions, suspensions, capsules).
  • Previous supervisory or management experience in a GMP environment.
  • Ability to write, review, and maintain SOPs.
  • Confident with documentation, email communication, and regulatory standards.
  • GPhC registration preferred but not essential if equivalent GMP aseptic production experience can be demonstrated.


What’s on Offer

  • 25 days annual leave, pension, and overtime pay.
  • A collaborative, supportive environment with fast feedback and interview turnaround.
  • The chance to play a visible, high-responsibility role in shaping early-phase clinical research.

This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Associate - Oncology Trials

WC2R 1LA London, London £60000 Annually WhatJobs

Posted 10 days ago

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Job Description

full-time
Our client, a leading global pharmaceutical company dedicated to developing life-saving therapies, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dynamic oncology clinical development team. This role is primarily office-based at their vibrant headquarters in **London, England, UK**, with opportunities for occasional site visits and remote work as project needs dictate. You will play a critical role in overseeing the execution of complex Phase I-IV clinical trials, ensuring compliance with regulatory standards and contributing to the successful progression of novel cancer treatments from trial initiation to database lock.

Key Responsibilities:
  • Conduct site initiation, interim monitoring, and close-out visits in accordance with Good Clinical Practice (GCP) and protocol requirements.
  • Ensure the quality, accuracy, and integrity of clinical data collected at investigational sites.
  • Verify that all investigational sites are adequately supplied with study supplies and informed about protocol requirements.
  • Oversee patient recruitment and retention efforts at assigned clinical sites.
  • Build and maintain strong working relationships with investigators, site staff, and other stakeholders.
  • Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA) and internal company policies.
  • Prepare and present study-related materials to site staff during initiation visits and regular calls.
  • Identify and resolve site-level issues and escalate critical problems as necessary.
  • Review and approve site visit reports and other study documentation.
  • Contribute to the development of clinical trial protocols, case report forms (CRFs), and other study documents.
  • Manage multiple clinical trials and study sites concurrently.
  • Stay updated on oncology research trends and regulatory guidelines.
Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Master's degree or equivalent experience preferred.
  • Minimum of 5 years of progressive experience as a Clinical Research Associate, with a significant focus on oncology trials.
  • Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
  • Demonstrated experience in monitoring clinical trials from initiation to close-out.
  • Excellent knowledge of oncology drug development and clinical trial designs.
  • Strong analytical and problem-solving skills with meticulous attention to detail.
  • Exceptional communication, interpersonal, and negotiation skills.
  • Ability to travel to clinical sites as required (approximately 40-60% travel).
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Ability to work independently and manage time effectively.
  • A proactive approach to problem-solving and a commitment to patient safety and data integrity.
This is a vital role within a globally recognized pharmaceutical leader, offering the chance to significantly impact the development of next-generation cancer therapies. The successful candidate will be a highly motivated and experienced CRA, dedicated to clinical excellence and eager to contribute to groundbreaking research within our client's London-based operations.
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Clinical Trial Manager

London, London Blackfield Associates

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Job Description

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. The successful candidate will excel in fast-paced, dynamic biotech settings and be committed to driving trials that meet the highest standards of quality, compliance, and operational excellence.


Responsibilities:


  • Lead the design, start-up, and execution of clinical trials, ensuring projects are completed on schedule, within scope, and aligned with budgetary expectations.
  • Serve as the primary sponsor contact for CROs, investigators, and providers.
  • Oversee CRO performance, including reviewing monitoring outputs and KPIs.
  • Work closely with Regulatory Affairs on ethics/regulatory submissions, ensuring alignment with ICH-GCP guidelines and current UK/EU regulations.
  • Maintain trial inspection readiness, overseeing safety reporting, audit response, and vendor governance.
  • Develop and review protocols, informed consent forms, and study reports.
  • Drive risk management, issue resolution, and collaboration across cross-functional teams.
  • Play an active role in refining operational processes and SOPs within the Clinical Operations function.


Requirements:


  • Bachelor’s degree (or equivalent) in a life science or health-related discipline.
  • Minimum of 8 years in clinical trial management across pharma, biotech, or CROs.
  • Site monitoring experience or proven ability to critically evaluate CRO monitoring performance.
  • In-depth understanding of ICH-GCP and global regulatory requirements, with strong understanding of upcoming UK/EU regulatory changes (e.g., UK CTR 2026).
  • Demonstrated success in managing CROs and vendors, including financial oversight.
  • Skilled at balancing multiple priorities and tight timelines.
  • Proficient in navigating lean, fast-paced environments; direct experience in biotech settings is valued.
  • Strong interpersonal and communication skills, with proven ability to manage internal stakeholders with accountability and transparency.
  • Able to work on-site in central London in a hybrid capacity.
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Clinical Trial Manager

London, London Blackfield Associates

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Job Description

Job Description

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. The successful candidate will excel in fast-paced, dynamic biotech settings and be committed to driving trials that meet the highest standards of quality, compliance, and operational excellence.


Responsibilities:


  • Lead the design, start-up, and execution of clinical trials, ensuring projects are completed on schedule, within scope, and aligned with budgetary expectations.
  • Serve as the primary sponsor contact for CROs, investigators, and providers.
  • Oversee CRO performance, including reviewing monitoring outputs and KPIs.
  • Work closely with Regulatory Affairs on ethics/regulatory submissions, ensuring alignment with ICH-GCP guidelines and current UK/EU regulations.
  • Maintain trial inspection readiness, overseeing safety reporting, audit response, and vendor governance.
  • Develop and review protocols, informed consent forms, and study reports.
  • Drive risk management, issue resolution, and collaboration across cross-functional teams.
  • Play an active role in refining operational processes and SOPs within the Clinical Operations function.


Requirements:


  • Bachelor’s degree (or equivalent) in a life science or health-related discipline.
  • Minimum of 8 years in clinical trial management across pharma, biotech, or CROs.
  • Site monitoring experience or proven ability to critically evaluate CRO monitoring performance.
  • In-depth understanding of ICH-GCP and global regulatory requirements, with strong understanding of upcoming UK/EU regulatory changes (e.g., UK CTR 2026).
  • Demonstrated success in managing CROs and vendors, including financial oversight.
  • Skilled at balancing multiple priorities and tight timelines.
  • Proficient in navigating lean, fast-paced environments; direct experience in biotech settings is valued.
  • Strong interpersonal and communication skills, with proven ability to manage internal stakeholders with accountability and transparency.
  • Able to work on-site in central London in a hybrid capacity.

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Clinical Trial Supply Manager

Uxbridge, London Hobson Prior

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Job Description

Hobson Prior is seeking a Clinical Trial Supply Manager to join a dynamic team in Uxbridge, UK. In this role, you will play a key part in managing the supply chain for investigational products, ensuring timely delivery and alignment with clinical study goals. This position involves collaboration with internal teams and external partners to support global clinical trials in the cell and gene therapy/biologics space.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Develop and maintain supply strategies for investigational products based on clinical and regulatory requirements.
  • Work closely with internal teams and external vendors to ensure all supply needs are met.
  • Plan and communicate supply chain strategies to align with clinical study objectives.
  • Monitor inventory, analyze drug usage, and adjust forecasts as needed.
  • Oversee manufacturing, packaging, and labeling requests to meet protocol and regulatory standards.
  • Support use date extensions and ensure compliance with country-specific regulations.
  • Participate in meetings to provide updates, highlight risks, and propose mitigation strategies.
  • Manage distribution strategies and maintain supply levels at depots and clinical sites.
  • Collaborate on budget planning and procurement of commercial drugs.
  • Act as the primary contact for clinical supply matters related to assigned studies.
  • Ensure inspection readiness by preparing necessary documentation and addressing product complaints or deviations.

Key Skills and Requirements:

  • Strong understanding of global drug development processes and regulatory requirements.
  • Proficient in forecasting, planning, and supply chain management.
  • Knowledge of manufacturing, packaging, labeling, and logistics processes.
  • Familiarity with industry systems such as IVRS and CTMS.
  • Excellent communication, negotiation, and project management skills.
  • Ability to analyze issues, resolve conflicts, and build consensus within teams.
  • Experience in managing budgets and working with external vendors.

For more information, please contact Emma Miles .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

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Clinical Trial Manager (CTM)

Uxbridge, London Gilead Sciences, Inc.

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Job Description

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
**The Position**
Careers within the Clinical Operations team offers individuals the opportunity to develop their knowledge & experience rapidly whilst enjoying a supportive and team-focused working environment. Kite and Gilead's operational model allows each Clinical Operations professional to make a genuine impact on the business and ultimately our ability to deliver live changing therapeutics to those in need.
An exciting and challenging opportunity has arisen to join the European Headquarters based in Stockley Park, Uxbridge as a Clinical Trial Manager to be responsible for the management of European and/or global activities on assigned study(ies) within the Cell Therapy Area. **This role is Hybrid and requires 3 days per week at our Uxbridge offices**
**Essential Duties and Job Functions:**
+ Manages European component of global Phases II-III outsourced studies.
+ Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports.
+ Maintains study timelines.
+ Contributes to development of study budget.
+ Contributes to development of RFPs and participate in selection of CROs/vendors.
+ Manages CROs/vendors.
+ Coordinates review of data listings and preparation of interim/final clinical study reports.
+ May contribute to development of abstracts, presentations, and manuscripts,
+ Ensures effectiveness of site budget/contract process.
+ May be asked to train CROs, vendors, investigators, and study coordinators on study requirements and cell therapy logistics.
+ Conducts oversight monitoring visits as required.
+ Assists in determining the activities to support a project's priorities within functional area.
+ Coordinates and supervises all aspects of a clinical study.
+ Under supervision, may design scientific communications within the company.
+ Contributes to Clinical Operations Europe team activities & initiatives
+ May serve as a resource for others within the company for clinical trials management expertise.
+ Under general supervision, is able to examine functional issues from an organizational perspective.
+ **Specific Responsibilities:**
+ Works with Clinical Program Managers and Global Clinical Trial Leads to manage the European component of global clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes. There might also be scope for global trial management.
+ Interacts with cross-functional teams internally and externally to ensure trial progress.
+ Will incorporate study logistics and planning to accomplish study objectives.
+ Will serve as the primary point of contact for CROs, addressing questions and applying knowledge to resolve problems
+ **Essential Functions:**
+ Oncology/Cell Therapy experience is highly preferable.
+ Must have multinational (preferably EU) clinical trials experience including study management/coordination.
+ Monitoring experience highly desirable as site oversight monitoring visits will be required.
+ Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
+ Must be able to generally understand, interpret, and explain protocol requirements to others.
+ Must be able to prioritize multiple tasks.
+ Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision.
+ Must have a general, functional expertise to support SOP development and implementation.
+ Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.
+ Excellent teamwork, communication, decision-making and organizational skills are required.
+ International travel is required (up to approximately 20%)
+ 3 days per week at Stockley Park
**_Gilead/Kite Core Values_**
INTEGRITY - Doing What's Right
INCLUSION - Encouraging Diversity
TEAMWORK - Working Together
EXCELLENCE - Being Your Best
ACCOUNTABILITY - Taking Personal Responsibility
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
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Clinical Trial Supply Manager

Uxbridge, London Hobson Prior

Posted today

Job Viewed

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Job Description

Job Description

Hobson Prior is seeking a Clinical Trial Supply Manager to join a dynamic team in Uxbridge, UK. In this role, you will play a key part in managing the supply chain for investigational products, ensuring timely delivery and alignment with clinical study goals. This position involves collaboration with internal teams and external partners to support global clinical trials in the cell and gene therapy/biologics space.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Develop and maintain supply strategies for investigational products based on clinical and regulatory requirements.
  • Work closely with internal teams and external vendors to ensure all supply needs are met.
  • Plan and communicate supply chain strategies to align with clinical study objectives.
  • Monitor inventory, analyze drug usage, and adjust forecasts as needed.
  • Oversee manufacturing, packaging, and labeling requests to meet protocol and regulatory standards.
  • Support use date extensions and ensure compliance with country-specific regulations.
  • Participate in meetings to provide updates, highlight risks, and propose mitigation strategies.
  • Manage distribution strategies and maintain supply levels at depots and clinical sites.
  • Collaborate on budget planning and procurement of commercial drugs.
  • Act as the primary contact for clinical supply matters related to assigned studies.
  • Ensure inspection readiness by preparing necessary documentation and addressing product complaints or deviations.

Key Skills and Requirements:

  • Strong understanding of global drug development processes and regulatory requirements.
  • Proficient in forecasting, planning, and supply chain management.
  • Knowledge of manufacturing, packaging, labeling, and logistics processes.
  • Familiarity with industry systems such as IVRS and CTMS.
  • Excellent communication, negotiation, and project management skills.
  • Ability to analyze issues, resolve conflicts, and build consensus within teams.
  • Experience in managing budgets and working with external vendors.

For more information, please contact Emma Miles .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - -policy.

This advertiser has chosen not to accept applicants from your region.

Neuroscience PhD Clinical Trial Coordinator

London, London Meet Life Sciences

Posted today

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Job Description

A leading Clinical Research Organization (CRO) is seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position within its Clinical Trial Management team . This position is available across several key European locations — London, Munich, Milan, and Madrid — offering candidates the opportunity to work in a highly collaborative and international environment. This is an excellent opportunity for recent PhD graduates to transition from academia into the clinical research and drug development industry , applying strong analytical and scientific skills to the management and coordination of global clinical studies . The successful candidate will receive comprehensive training , gain exposure to international projects, and have the potential for fast-tracked career development into Clinical Trial Management (CTM). Key Responsibilities Collaborate on global study activities , working closely with Project Coordinators and Clinical Trial Managers to ensure operational excellence. Maintain accurate and timely project documentation and status reports within the Clinical Trial Management System (CTMS). Communicate effectively with internal stakeholders, Sponsors, study sites, and third-party vendors. Support regulatory and quality control processes , ensuring full compliance with SOPs and ICH-GCP standards. Manage study supplies, timelines, and deliverables in line with project milestones. Coordinate and facilitate project meetings, including agenda preparation and production of meeting minutes. Contribute to maintaining high-quality documentation and process efficiency across assigned studies. Qualifications PhD in Life Sciences (or a related scientific field). Excellent communication and presentation skills, with fluency in English. Strong organizational, analytical, and problem-solving capabilities. Ability to thrive in a fast-paced, global, and team-oriented environment. Prior experience in the CRO, pharmaceutical, or biotechnology sector is beneficial but not essential. About the Company This organization is a global, full-service Clinical Research Organization (CRO) supporting Phase I–IV clinical development for biotechnology, pharmaceutical, and medical device clients. Its mission is to accelerate the development of innovative, safe, and effective medical therapies through scientific rigor, operational discipline, and cross-functional collaboration . With operations spanning 40 countries and therapeutic expertise in oncology, cardiology, CNS, metabolic, and infectious diseases , the company is committed to advancing clinical research and improving patient outcomes worldwide. Why Join Locations: London, Munich, Milan, and Madrid Competitive compensation and benefits package Flexible, hybrid working model Structured training and professional development pathways Inclusive, collaborative international culture Company-sponsored recognition and wellness initiatives
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