Location: Witney
Salary: £55,000 per annum
...
summary
Location: Witney
Salary: £55,000 per annum
...
We are seeking a Senior Scientist to join a Clinical Science team on a 12-month contract. This role offers an exciting opportunity to provide scientific expertise and support across a global business, contributing to the development and delivery of high-quality clinical documentation.
You will play a key role in supporting regulatory and market access activities, working closely with cross-functional teams to deliver robust clinical evidence in line with EU regulatory expectations.
Lead the collation, critical appraisal, and analysis of clinical evidence, including scientific literature
Author and review high-quality technical documentation and product summaries
Contribute to the development of Clinical Evaluation and Performance Evaluation documentation
Support cross-functional initiatives including product registrations, reimbursement submissions, and strategic evaluations
Collaborate with global stakeholders across Regulatory, Medical, and Market Access teams
Mentor junior team members and support continuous process improvement
Educated to degree level in a scientific discipline (BSc minimum; MSc, PhD, or equivalent desirable)
Proven experience in technical/scientific writing and literature appraisal
Strong analytical, critical thinking, and communication skills
Comfortable working in a fast-paced, collaborative, matrix environment
Proactive, organised, and able to work independently and as part of a team
Experience with EU MDR and Clinical Evaluation processes is desirable but not essential
This is an excellent opportunity to join a supportive, high-performing team where you can apply your scientific expertise, develop your regulatory knowledge, and make a meaningful contribution to impactful clinical projects.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Location: Witney
Salary: £55,000 per annum
Contract: 12-month
We are seeking a Senior Scientist to join a Clinical Science team on a 12-month contract. This role offers an exciting opportunity to provide scientific expertise and support across a global business, contributing to the development and delivery of high-quality clinical documentation.
You will play a key role in supporting regulatory and market access activities, working closely with cross-functional teams to deliver robust clinical evidence in line with EU regulatory expectations.
Lead the collation, critical appraisal, and analysis of clinical evidence, including scientific literature
Author and review high-quality technical documentation and product summaries
Contribute to the development of Clinical Evaluation and Performance Evaluation documentation
Support cross-functional initiatives including product registrations, reimbursement submissions, and strategic evaluations
Collaborate with global stakeholders across Regulatory, Medical, and Market Access teams
Mentor junior team members and support continuous process improvement
Educated to degree level in a scientific discipline (BSc minimum; MSc, PhD, or equivalent desirable)
Proven experience in technical/scientific writing and literature appraisal
Strong analytical, critical thinking, and communication skills
Comfortable working in a fast-paced, collaborative, matrix environment
Proactive, organised, and able to work independently and as part of a team
Experience with EU MDR and Clinical Evaluation processes is desirable but not essential
This is an excellent opportunity to join a supportive, high-performing team where you can apply your scientific expertise, develop your regulatory knowledge, and make a meaningful contribution to impactful clinical projects.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
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