Clinical Research Scientist
Posted on Jun 25, 2026 by CV-Library
Witney, Oxfordshire, United Kingdom
Pharmaceutical
Immediate Start
£32.5k - £32.5k Annual
Temporary
Job Title: Clinical Research Scientist (12-Month Contract)
Location: Witney, Oxfordshire
Salary: £32,500 per annum
Position Type: 12-Month Fixed Term Contract
Category: Clinical Affairs / Scientific Writing / Medical Devices & Regulation
About the Role
Are you a science graduate or an industry professional looking to build a career in the high-demand medical device sector? We have an excellent opportunity for a Clinical Scientist to join a world-class clinical operations team at a major manufacturing site in Witney.
In this vital role, you will be responsible for ensuring the timely delivery of high-quality technical reports in accordance with MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) guidelines. Your work will directly support CE marking, enabling the continued global supply of life-changing healthcare products.
This role focuses heavily on the critical review and appraisal of clinical data, alongside the preparation of clear, accurate scientific documentation. It's a fantastic environment for someone eager to develop deep expertise in scientific writing, data evaluation, and regulatory compliance.
Key Responsibilities:
Data Appraisal & Review: Gather, critically review, and assess clinical evidence from a range of sources, including scientific literature and post-market clinical follow-up data.
Technical Writing: Compile, write, and edit high-quality technical documentation and clinical evaluation reports to meet strict EU and global regulatory standards.
Competitor Analysis: Evaluate data for both internal medical devices and competitor products to support clinical safety arguments.
Data Presentation: Take complex data sets and present findings in an impactful, engaging, and clear way to cross-functional teams.
Continuous Improvement: Participate in team initiatives aimed at streamlining documentation workflows and optimizing data analysis procedures.
What We Are Looking For:
Education: A higher education qualification (BSc, MSc, or equivalent) in a technical, medical, or scientific discipline.
Writing & Communication: Strong communication skills with an excellent grasp of scientific/technical writing and a sharp eye for detail.
Agility: The ability to adapt quickly to changing project priorities and fast-paced deadlines.
Tech Savvy: Strong IT literacy, including high proficiency in Microsoft Office applications. Experience with data tools like Power BI or automation tools like Power Automate is highly desirable.
Industry Experience (Preferred): Ideally, some prior industry-based experience working within a scientific, laboratory, or highly regulated environment (e.g., Pharmaceuticals, ISO settings, or Medical Devices).
Benefits & Site Perks:
Onsite parking
Electric vehicle charging points
Subsidised canteen
Free premium coffee facilities
Randstad Business Support is acting as an Employment Business in relation to this vacancy
Location: Witney, Oxfordshire
Salary: £32,500 per annum
Position Type: 12-Month Fixed Term Contract
Category: Clinical Affairs / Scientific Writing / Medical Devices & Regulation
About the Role
Are you a science graduate or an industry professional looking to build a career in the high-demand medical device sector? We have an excellent opportunity for a Clinical Scientist to join a world-class clinical operations team at a major manufacturing site in Witney.
In this vital role, you will be responsible for ensuring the timely delivery of high-quality technical reports in accordance with MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) guidelines. Your work will directly support CE marking, enabling the continued global supply of life-changing healthcare products.
This role focuses heavily on the critical review and appraisal of clinical data, alongside the preparation of clear, accurate scientific documentation. It's a fantastic environment for someone eager to develop deep expertise in scientific writing, data evaluation, and regulatory compliance.
Key Responsibilities:
Data Appraisal & Review: Gather, critically review, and assess clinical evidence from a range of sources, including scientific literature and post-market clinical follow-up data.
Technical Writing: Compile, write, and edit high-quality technical documentation and clinical evaluation reports to meet strict EU and global regulatory standards.
Competitor Analysis: Evaluate data for both internal medical devices and competitor products to support clinical safety arguments.
Data Presentation: Take complex data sets and present findings in an impactful, engaging, and clear way to cross-functional teams.
Continuous Improvement: Participate in team initiatives aimed at streamlining documentation workflows and optimizing data analysis procedures.
What We Are Looking For:
Education: A higher education qualification (BSc, MSc, or equivalent) in a technical, medical, or scientific discipline.
Writing & Communication: Strong communication skills with an excellent grasp of scientific/technical writing and a sharp eye for detail.
Agility: The ability to adapt quickly to changing project priorities and fast-paced deadlines.
Tech Savvy: Strong IT literacy, including high proficiency in Microsoft Office applications. Experience with data tools like Power BI or automation tools like Power Automate is highly desirable.
Industry Experience (Preferred): Ideally, some prior industry-based experience working within a scientific, laboratory, or highly regulated environment (e.g., Pharmaceuticals, ISO settings, or Medical Devices).
Benefits & Site Perks:
Onsite parking
Electric vehicle charging points
Subsidised canteen
Free premium coffee facilities
Randstad Business Support is acting as an Employment Business in relation to this vacancy
Reference: 225294501
https://jobs.careeraddict.com/post/113465076
Clinical Research Scientist
Posted on Jun 25, 2026 by CV-Library
Witney, Oxfordshire, United Kingdom
Pharmaceutical
Immediate Start
£32.5k - £32.5k Annual
Temporary
Job Title: Clinical Research Scientist (12-Month Contract)
Location: Witney, Oxfordshire
Salary: £32,500 per annum
Position Type: 12-Month Fixed Term Contract
Category: Clinical Affairs / Scientific Writing / Medical Devices & Regulation
About the Role
Are you a science graduate or an industry professional looking to build a career in the high-demand medical device sector? We have an excellent opportunity for a Clinical Scientist to join a world-class clinical operations team at a major manufacturing site in Witney.
In this vital role, you will be responsible for ensuring the timely delivery of high-quality technical reports in accordance with MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) guidelines. Your work will directly support CE marking, enabling the continued global supply of life-changing healthcare products.
This role focuses heavily on the critical review and appraisal of clinical data, alongside the preparation of clear, accurate scientific documentation. It's a fantastic environment for someone eager to develop deep expertise in scientific writing, data evaluation, and regulatory compliance.
Key Responsibilities:
Data Appraisal & Review: Gather, critically review, and assess clinical evidence from a range of sources, including scientific literature and post-market clinical follow-up data.
Technical Writing: Compile, write, and edit high-quality technical documentation and clinical evaluation reports to meet strict EU and global regulatory standards.
Competitor Analysis: Evaluate data for both internal medical devices and competitor products to support clinical safety arguments.
Data Presentation: Take complex data sets and present findings in an impactful, engaging, and clear way to cross-functional teams.
Continuous Improvement: Participate in team initiatives aimed at streamlining documentation workflows and optimizing data analysis procedures.
What We Are Looking For:
Education: A higher education qualification (BSc, MSc, or equivalent) in a technical, medical, or scientific discipline.
Writing & Communication: Strong communication skills with an excellent grasp of scientific/technical writing and a sharp eye for detail.
Agility: The ability to adapt quickly to changing project priorities and fast-paced deadlines.
Tech Savvy: Strong IT literacy, including high proficiency in Microsoft Office applications. Experience with data tools like Power BI or automation tools like Power Automate is highly desirable.
Industry Experience (Preferred): Ideally, some prior industry-based experience working within a scientific, laboratory, or highly regulated environment (e.g., Pharmaceuticals, ISO settings, or Medical Devices).
Benefits & Site Perks:
Onsite parking
Electric vehicle charging points
Subsidised canteen
Free premium coffee facilities
Randstad Business Support is acting as an Employment Business in relation to this vacancy
Location: Witney, Oxfordshire
Salary: £32,500 per annum
Position Type: 12-Month Fixed Term Contract
Category: Clinical Affairs / Scientific Writing / Medical Devices & Regulation
About the Role
Are you a science graduate or an industry professional looking to build a career in the high-demand medical device sector? We have an excellent opportunity for a Clinical Scientist to join a world-class clinical operations team at a major manufacturing site in Witney.
In this vital role, you will be responsible for ensuring the timely delivery of high-quality technical reports in accordance with MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) guidelines. Your work will directly support CE marking, enabling the continued global supply of life-changing healthcare products.
This role focuses heavily on the critical review and appraisal of clinical data, alongside the preparation of clear, accurate scientific documentation. It's a fantastic environment for someone eager to develop deep expertise in scientific writing, data evaluation, and regulatory compliance.
Key Responsibilities:
Data Appraisal & Review: Gather, critically review, and assess clinical evidence from a range of sources, including scientific literature and post-market clinical follow-up data.
Technical Writing: Compile, write, and edit high-quality technical documentation and clinical evaluation reports to meet strict EU and global regulatory standards.
Competitor Analysis: Evaluate data for both internal medical devices and competitor products to support clinical safety arguments.
Data Presentation: Take complex data sets and present findings in an impactful, engaging, and clear way to cross-functional teams.
Continuous Improvement: Participate in team initiatives aimed at streamlining documentation workflows and optimizing data analysis procedures.
What We Are Looking For:
Education: A higher education qualification (BSc, MSc, or equivalent) in a technical, medical, or scientific discipline.
Writing & Communication: Strong communication skills with an excellent grasp of scientific/technical writing and a sharp eye for detail.
Agility: The ability to adapt quickly to changing project priorities and fast-paced deadlines.
Tech Savvy: Strong IT literacy, including high proficiency in Microsoft Office applications. Experience with data tools like Power BI or automation tools like Power Automate is highly desirable.
Industry Experience (Preferred): Ideally, some prior industry-based experience working within a scientific, laboratory, or highly regulated environment (e.g., Pharmaceuticals, ISO settings, or Medical Devices).
Benefits & Site Perks:
Onsite parking
Electric vehicle charging points
Subsidised canteen
Free premium coffee facilities
Randstad Business Support is acting as an Employment Business in relation to this vacancy
Reference: 225294501
Share this job:
Alert me to jobs like this:
Amplify your job search:
Expert career advice
Increase interview chances with our downloads and specialist services.
Visit Blog