Senior Scientist, Medical Writing (MD)

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our team as a Senior Scientist, Medical Writing (MD) on a permanent basis.

Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!

Position Overview: The Senior Scientist, Medical Writing (MD) serves as the clinical and scientific subject matter expert (SME) supporting the development of pre-clinical research publications. This role provides strategic scientific oversight and quality review of manuscripts authored by medical writers, ensuring scientific accuracy, clinical relevance, publication readiness, and alignment with current cardiovascular practice.

• Serve as the primary clinical expert for pre-clinical research publications.

• Prepares, writes, and edits systematic literature reviews through the creation of protocols and reports in order to synthesize and analyze the clinical data from medical and scientific publications reporting on a range of devices and treatment options.

• Participates in core process steps including data search, screening, data extraction, and analysis utilizing established software and tools.

• Provide clinical interpretation of study findings and assess their potential relevance to patient care and future clinical application.

• Advise teams on cardiovascular disease states, treatment pathways, current standards of care, and emerging technologies, correlating them to the source documents, whenever necessary.

• Support publication strategy for cardiovascular device portfolio.

• Perform comprehensive scientific and clinical review of manuscript drafts developed by medical writers.

• Identify gaps, inconsistencies, and unsupported claims.

• Ensure manuscripts are suitable for submission to high-impact peer-reviewed journals.

• Collaborate with medical writers during publication planning and manuscript development.

• Participate in author meetings and publication review discussions.

• Participates in creation of medical training materials and programs that are used to support initial and ongoing training for new employees (e.g., medical writers).

• Act as backup medical writer.

• MD, DO, MBBS, or equivalent medical degree.

• Board certification or specialty training in a cardiovascular discipline is preferred.

• At least 5 years of clinical, scientific, or medical writing experience.

• Experience interpreting pre-clinical, translational, and clinical study data.

• Familiarity with FDA, EU MDR, and global medical device regulatory requirements.

• Experience working within a CRO, medical device manufacturer academic research organization, or cardiovascular research center.

• Flexible Working Hours

• Full performance and development process with end of year reviews

• Team events and end of year party

• Employee satisfaction survey - your feedback is important for continuous improvement

• Health Insurance

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we