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Clinical scientist

Cambridge
Proclinical
Clinical scientist
Posted: 16 February
Offer description

Elevate your career while advancing patient care and be the force behind life-changing technology with this Clinical Scientist position!

Proclinical is seeking a Clinical Scientist to develop strong clinical evidence, assist regulatory processes, and enhance scientific content that supports impactful healthcare advancements. You'll work as part of a fast‑moving, cross‑functional team driving progress in respiratory medicine.

Responsibilities:

1. Develop and implement clinical research strategies to support medical device regulation and adoption.
2. Design, plan, and manage research programs, including drafting study protocols, ethics submissions, and project charters.
3. Oversee study implementation, monitoring, and reporting, including site visits and stakeholder communications.
4. Conduct systematic literature reviews and analyze clinical processes to recommend improvements.
5. Write and review scientific content such as peer-reviewed publications, conference abstracts, white papers, and educational materials.
6. Collaborate with internal teams to manage relationships with key clinical stakeholders and opinion leaders.
7. Support clinical evaluation processes, including drafting Clinical Evaluation Plans, Reports, and Post-Market Clinical Follow-up documentation.

Key Skills and Requirements:

8. Strong written and verbal communication skills, with the ability to simplify complex scientific concepts for diverse audiences.
9. Proficiency in research design, data interpretation, and systematic literature searches.
10. Excellent organizational and project management skills, with the ability to meet deadlines.
11. A collaborative mindset with strong interpersonal skills and attention to detail.
12. Bachelor's degree in a scientific or clinical field.
13. Experience in scientific writing, including peer-reviewed publications.
14. Proven track record in designing or managing clinical research projects.
15. Familiarity with quality management systems (e.g., ISO 13485 or ISO 9001) and medical device products is advantageous.

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