Research & Development Administrator - Strand, London, WC2R 2LS

WC2R 2LS London, London Kings College London

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Research & Development Administrator - Strand, London, WC2R 2LS About us:

The Joint Research and Development (R&D) Office supports researchers at the Institute of Psychiatry, Psychology & Neuroscience and South London and Maudsley NHS Foundation Trust to conduct research in the Trust.

The R&D team ensures that all studies taking place within the Trust meet the required ethical, contractual, and regulatory standards before they begin.

We are dedicated to helping deliver high-quality, ethically sound research by providing expert advice and practical guidance.

We are based in the Institute of Psychiatry, Psychology & Neuroscience at the Denmark Hill Campus, South East London.

About the role:

This is an exciting opportunity for an enthusiastic, organised and motivated individual who is interested in working in an NHS or university environment supporting UK health research.

The post-holder will have a key role in facilitating research management and governance processes required under the UK Policy Framework for Health and Social Care Research and relevant legislation. They will be the first point of contact for R&D enquiries and work within the R&D team to deliver a first-class advisory and support service to researchers.

Experience in working in NHS R&D or a university research support role is desirable but not essential, as support and training will be provided to the post-holder to develop their role. The successful candidate will have outstanding organisational and communication skills, with excellent computer literacy (Excel, Access, Outlook) and the ability to process complex information. The ability to work effectively as part of a team is essential, as well as the motivation for independent hybrid working.

This is an opportunity to work in an R&D Office with experienced staff, providing an opportunity to develop knowledge and skills in R&D in both an NHS and university context. The successful candidate will provide high level administrative support within the R&D office by acting as a first point of contact for R&D enquiries, triaging professional expert advice to research investigators, and organising meetings and diaries.

This is a part time post (21 hours per week), and you will be offered an indefinite contract. 

As the role is part time, please note that the salary listed in the advert will be amended accordingly (pro rata).

Working days/hours to be discussed.

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Senior Research Development Manager - Strand, London, WC2R 2LS

WC2R 2LS London, London Kings College London

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Senior Research Development Manager - Strand, London, WC2R 2LS About Us

The School has secured multi-million-pound research funding and maintains strong partnerships with UK and international universities, the NHS, charitable organisations, and industry partners. The vision is to establish the School as a world leader in healthcare engineering.

About The Role

The Research Development Manager is a senior role within the School of Biomedical Engineering & Imaging Sciences, responsible for driving large-scale, high-profile healthcare engineering grants that deliver real-world patient benefits and measurable impact. Working closely with the Head of School, Heads of Research Departments, academic and research staff, and external stakeholders, this role will play a pivotal part in securing funding, fostering strategic collaborations, and facilitating the translation of healthcare engineering innovations into clinical applications.

The Research Development Manager will be instrumental in realizing the School’s vision by providing strategic and operational support, they will support the development and submission of competitive grant applications, fellowships, and funding proposals to governmental agencies, Charities, and industry sponsors. The role requires a strong scientific background, exceptional writing skills, and the ability to translate complex research concepts into clear, compelling narratives tailored to funder priorities.

This is a full time (35 Hours per week), and you will be offered an indefinite contract.

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Postdoctoral Research Associate

London, London King's College London

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Postdoctoral Research Associate


Location: Bush House, London, UK (Remote/Hybrid options not available)

Starting Date: Starting date from November 3, 2025

Visa sponsorship available

Application deadline: 23 October 2025

Grade and Salary: £46,189 per annum, including London Weighting Allowance


We are looking for a highly motivated Postdoctoral Research Associate to join the Vision & Human-Robot Interaction (VHR) Group at King’s College London. The role focuses on translating a tendon-driven soft robotic exoskeleton glove designed for home-based hand rehabilitation in stroke survivors.


Responsibilities :

  • Lead integration of embedded control systems and multimodal intent detection
  • Contribute to the control software and monitoring interface development
  • Support clinical user trials, including data collection and analysis
  • Collaborate with a multidisciplinary team of robotics researchers and clinicians


Qualifications :

Essential:

  • PhD in Robotics, Computer Science, Biomedical Engineering, or related field (candidates awaiting viva considered)
  • Proven experience in mechanical design of exoskeletons, wearable robotics, or soft actuators
  • Proficiency in C++ and Python, with experience in ROS or other robotics frameworks
  • At least one peer-reviewed publication in robotics, AI, or biomedical engineering
  • Excellent written and verbal communication skills


Desirable:

  • Involvement in user and clinical studies or translational research
  • Familiarity with medical device certifications (ISO 13485) or CE/UKCA regulations


Apply by sending your CV, using this link:


#Robotics #HumanRobotInteraction #RehabilitationRobotics #AI #MedicalDevices #Postdoc #ResearchOpportunity

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Postdoctoral Research Associate

London, London King's College London

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Job Description

Job Description

Postdoctoral Research Associate


Location: Bush House, London, UK (Remote/Hybrid options not available)

Starting Date: Starting date from November 3, 2025

Visa sponsorship available

Application deadline: 23 October 2025

Grade and Salary: £46,189 per annum, including London Weighting Allowance


We are looking for a highly motivated Postdoctoral Research Associate to join the Vision & Human-Robot Interaction (VHR) Group at King’s College London. The role focuses on translating a tendon-driven soft robotic exoskeleton glove designed for home-based hand rehabilitation in stroke survivors.


Responsibilities :

  • Lead integration of embedded control systems and multimodal intent detection
  • Contribute to the control software and monitoring interface development
  • Support clinical user trials, including data collection and analysis
  • Collaborate with a multidisciplinary team of robotics researchers and clinicians


Qualifications :

Essential:

  • PhD in Robotics, Computer Science, Biomedical Engineering, or related field (candidates awaiting viva considered)
  • Proven experience in mechanical design of exoskeletons, wearable robotics, or soft actuators
  • Proficiency in C++ and Python, with experience in ROS or other robotics frameworks
  • At least one peer-reviewed publication in robotics, AI, or biomedical engineering
  • Excellent written and verbal communication skills


Desirable:

  • Involvement in user and clinical studies or translational research
  • Familiarity with medical device certifications (ISO 13485) or CE/UKCA regulations


Apply by sending your CV, using this link: kclp/erq jobspecversion 4.displayform?p company=1&pinternal external=E&pdisplay inirish=N&p processtype=&p applicantno=&p formprofile detail=&pdisplay applyind=Y&p refreshsearch=Y&p recruitment_id=


#Robotics #HumanRobotInteraction #RehabilitationRobotics #AI #MedicalDevices #Postdoc #ResearchOpportunity

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Quantitative Research Associate

London, London Validus Risk Management

Posted 15 days ago

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Permanent

We are looking for an Associate Quantitative Analyst to join our Quantitative Research team.

This team is responsible for developing and validating the financial models that drive our market risk analytics, with a particular focus on liquidity risk and credit charges in private market portfolios.

As part of a growing quantitative team—alongside Quant Development, Quant Strategies, and Risk Advisory—you will play a key role in shaping the firm’s expanding capabilities in credit and equity derivatives, building on our established expertise in interest rate and FX risk.

Key Responsibilities:

  • Design, develop, and document pricing and risk models for credit and equity derivatives as part of the firm’s strategic expansion in these areas.
  • Work closely with Quant Dev to integrate new models into our internal Python-based risk platform.
  • Support the Quant Strategies and Risk Advisory teams with model calibration, validation, and interpretation across private credit and equity-related exposures.
  • Contribute to liquidity risk modelling, credit charge calculation, and scenario analysis for private market portfolios.
  • Conduct research into new modelling methodologies and maintain awareness of market and regulatory developments.
  • Translate complex model outputs into actionable insights for both internal and external stakeholders.
  • Prepare technical documentation, testing frameworks, and presentation materials for model sign-off and client communication.

Requirements

  • Minimum 5 years of experience in a quantitative finance, risk modelling, or financial engineering role.
  • Master’s degree or higher in a quantitative/STEM field (e.g., Mathematics, Physics, Financial Engineering, Computer Science).
  • Practical experience with pricing and risk management of credit and/or equity derivatives, ideally across multiple asset classes.
  • Strong programming skills in Python for financial modelling and data analysis.
  • Solid understanding of market risk concepts including VaR, stress testing, sensitivities, and exposure analysis.
  • Ability to work independently on model design and testing, while collaborating effectively with cross-functional teams.
  • Excellent communication skills and the ability to explain quantitative results to non-specialist audiences.
  • Strong attention to detail and ability to manage multiple project streams.

Preferred Qualifications:

  • Experience with C++ or Rust for performance-critical quantitative modelling.
  • Familiarity with private market liquidity risk, credit charges, and illiquid portfolio analytics.
  • Exposure to interest rate and FX derivatives and related risk frameworks.

Benefits

Validus Risk Management is an independent technology-enabled advisory firm specialising in the management of FX, interest rate and other market risks. We work with institutional investors, fund managers, and portfolio companies to design and implement strategies to measure, manage and monitor financial market risk, using a market-tested combination of specialist consulting services, trade execution and innovative risk technology.

Working at Validus can offer an exciting opportunity for both personal development and professional growth. Share in our mission to become the largest and most respected specialist provider of financial market risk services in the world. Notable benefits include a competitive remuneration package (salary + bonus), health care, retirement plans, and financial support towards professional qualifications.

Our core company values are;

  • Accountability – Getting it done and owning the result.
  • Teamwork – We succeed by helping others succeed.
  • Integrity – We serve our clients; the responsibility is sacrosanct. 
  • Diversity – Diversity boosts creativity – creativity is our edge.
  • Kaizen – Strive to do things better. Innovation kills complacency.

Validus is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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Clinical Research Associate I

London, London Russell Tobin

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contract
Job title: Clinical Project Associate I Location: London Contract duration: 12 months Client: Pharmaceutical Job Purpose: The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively. Major Activities: • Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews. • Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible. • Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items) • Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration. • Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders. • Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization. • Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks. • Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices. Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group. Education and/or professional experience: • Bachelor’s degree in life sciences, public health, or a related field. Languages: • Fluent English (oral and written) Experience / Professional Requirements: • 2-3 years of experience in clinical research, project coordination or consultancy. • Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks • Strong organisational, project management and communication skills. • Proficiency in Microsoft Office and project management tools. • Delivery focus; reliable and respond promptly to requests • Ability to multi-task and prioritize • Strong attention to detail and highly organized • Successful relationship builder and communicator • Ability to work independently and collaboratively in a fast-paced environment. • Desirable: Experience with AI tools in clinical development
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Clinical Research Associate I

London, London Russell Tobin

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contract
Job title: Clinical Project Associate I Location: London Contract duration: 12 months Client: Pharmaceutical Job Purpose: The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively. Major Activities: • Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews. • Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible. • Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items) • Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration. • Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders. • Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization. • Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks. • Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices. Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group. Education and/or professional experience: • Bachelor’s degree in life sciences, public health, or a related field. Languages: • Fluent English (oral and written) Experience / Professional Requirements: • 2-3 years of experience in clinical research, project coordination or consultancy. • Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks • Strong organisational, project management and communication skills. • Proficiency in Microsoft Office and project management tools. • Delivery focus; reliable and respond promptly to requests • Ability to multi-task and prioritize • Strong attention to detail and highly organized • Successful relationship builder and communicator • Ability to work independently and collaboratively in a fast-paced environment. • Desirable: Experience with AI tools in clinical development
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Clinical Research Associate I

London, London Russell Tobin

Posted today

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Job Description

Job title: Clinical Project Associate I

Location: London

Contract duration: 12 months

Client: Pharmaceutical


Job Purpose:

The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively.


Major Activities:

Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews.

Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible.

Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items)

Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration.

Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders.

Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization.

Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks.

Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices.


Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group.


Education and/or professional experience:

• Bachelor’s degree in life sciences, public health, or a related field.


Languages:

• Fluent English (oral and written)


Experience / Professional Requirements:

• 2-3 years of experience in clinical research, project coordination or consultancy.

• Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks

• Strong organisational, project management and communication skills.

• Proficiency in Microsoft Office and project management tools.

• Delivery focus; reliable and respond promptly to requests

• Ability to multi-task and prioritize

• Strong attention to detail and highly organized

• Successful relationship builder and communicator

• Ability to work independently and collaboratively in a fast-paced environment.

• Desirable: Experience with AI tools in clinical development

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Research Associate | Market Intel

London, London Nicholson Glover

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Research Associate | Banking Market Intel | £28,000-36,000 DOE


**2nd Language Required**


Looking to build a meaningful career in international market intelligence?


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Research Associate - Infrastructure Insights

London, London Bentley Systems

Posted 2 days ago

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**Research Associate**
**Infrastructure Insights**
**Location:** UK or Ireland
**Work mode:** Home Based - Hybrid
**Position Summary:**
The **Research Associate - Infrastructure Insights** plays a key role in advancing Bentley's mission to inform and inspire positive change across the global infrastructure ecosystem. Sitting within the Infrastructure Policy & Advocacy (IPA) initiative, this role leads industry-insight monitoring and reporting for Bentley's leadership team.
You will design and manage a scalable research process to identify and track emerging trends in infrastructure markets, develop productive relationships with industry membership bodies, and deliver quarterly data-driven reports that help shape Bentley's strategic direction. This position offers the opportunity to collaborate across teams and ensure research outputs are accessible, inclusive, and aligned with Bentley's commitment to sustainability, innovation, and equity.
_Note: This role is internally titled_ **_Infrastructure Insights Lead_** _, reflecting its strategic scope and leadership responsibilities within the IPA initiative._
**Responsibilities:**
+ Lead the IPA's industry-insight monitoring and reporting function, developing a scalable process for market research and reporting that can grow across regions and business functions.
+ Conduct desk-based research and engage stakeholders - including industry associations and relevant bodies - to analyze:
+ Global developments across infrastructure sectors (transport, water, energy, etc.)
+ Infrastructure policy and investment trends in Bentley's key markets
+ Innovative funding, finance, and delivery models
+ Digital transformation trends in infrastructure
+ Synthesize research findings into quarterly insight reports, briefing notes, market scans, and landscape analyses to support Bentley's programs and partnerships.
+ Develop and maintain a knowledge base of relevant data sources, stakeholders, and industry initiatives, ensuring insights are accurate, timely, and broadly accessible to internal stakeholders.
+ Collaborate with cross-functional teams to support inclusive decision-making and knowledge sharing.
**Qualifications:**
+ Bachelor's degree in public policy, management, engineering, urban planning, economics, or a related field; Master's degree preferred but not required.
+ 5+ years of experience in research, consulting, or policy analysis, ideally within infrastructure or the built environment.
+ Strong analytical and critical thinking skills, with the ability to synthesize complex information into clear, actionable insights.
+ Excellent written and verbal communication skills in English (near-native fluency required); additional languages are a plus.
+ Self-starter with strong organizational skills, attention to detail, and a collaborative mindset.
+ Familiarity with infrastructure markets, public policy, and international business - or the ability to quickly learn and adapt.
+ Commitment to Bentley's values, including sustainability, innovation, and fostering an inclusive workplace.
+ We encourage candidates from diverse backgrounds to apply, even if you do not meet 100% of the listed qualifications.
**What We Offer:**
+ A great Team and culture - please see our colleague video .
+ An exciting career as an integral part of a world-leading software company providing solutions for architecture, engineering, and construction - watch this short documentary about how we got our start.
+ An attractive salary and benefits package.
+ A commitment to inclusion, belonging and colleague wellbeing through global initiatives and resource groups.
+ A company committed to making a real difference by advancing the world's infrastructure for better quality of life, where your contributions help build a more sustainable, connected, and resilient world. Discover our latest user success stories for an insight into our global impact.
**LI-BC #LI-Hybrid #LI-Remote**
 **About Bentley Systems**
Around the world, infrastructure professionals rely on software from Bentley Systems to help them design, build, and operate better and more resilient infrastructure for transportation, water, energy, cities, and more. Founded in 1984 by engineers for engineers, Bentley is the partner of choice for engineering firms and owner-operators worldwide, with software that spans engineering disciplines, industry sectors, and all phases of the infrastructure lifecycle. Through our digital twin solutions, we help infrastructure professionals unlock the value of their data to transform project delivery and asset performance. Opportunity Employer:**
Bentley is proud to be an equal opportunity employer and considers for employment all qualified applicants without regard to race, color, gender/gender identity, sexual orientation, disability, marital status, religion/belief, national origin, caste, age, or any other characteristic protected by local law or unrelated to job qualifications.
Equal Opportunity Employer/Minorities/Females/Veterans/Disabled
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