Senior Scientist, Medical Writing (MD)
Quick Summary
Serve as the primary clinical expert for pre-clinical research publications. Prepares, writes,
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.
Responsibilities
~1 min read- →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.
What We Offer
~1 min readOnce you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare!
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Location & Eligibility
Listing Details
- Posted
- August 15, 2026
- First seen
- August 15, 2026
- Last seen
- August 15, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 67%
- Scored at
- August 15, 2026
Signal breakdown
ClinChoice is a global full-service CRO that specializes in accelerating drug and device approvals across various healthcare sectors.
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