Sr Medical Scientist

Updated: September 16, 2025
Location: USA-NY-Remote
Job :

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

• We are passionate about developing our people through career development and progression, supportive line management, technical and therapeutic area training, peer recognition, and total rewards programs.
• We are committed to our Total Self culture – where you can authentically be yourself. Our culture unites us globally and we are dedicated to taking care of our people.
• We continuously build the company we all want to work for. By bringing together diverse thoughts, backgrounds, cultures, and perspectives, we create a place where everyone feels like they belong.

• Work with the Medical Director to develop Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans; engage external experts to gather necessary medical/scientific input.
• Provide support for observational study execution, including epidemiological, non-interventional, pragmatic, and low-interventional studies and research collaborations to ensure consistency of approach, conduct, monitoring, analysis, reporting, and oversight.
• Perform regular and ad‑hoc medical review of data listings and visualizations; analyze data to identify risks and trends; support documentation of medical reviews; proactively resolve review issues.
• Author medical data queries, review responses to queries, and approve query closure with the Medical Director.
• Assist the Medical Director with patient profile review, scientific review of other study‑level data, protocol deviation review, and creation of Medical Review Summary reports as needed.
• Partner with Medical Directors for medical data review and safety review meetings, including slide preparation.
• Identify issues timely, lead solution implementation, and/or escalate as appropriate; provide operational input on tactical study implementation in a global environment.
• Manage project scope, objectives, and quality of deliverables to meet milestones and timelines.
• Serve as the primary interface between the internal team, customers, and vendors in medical data review and eligibility review.
• Collaborate with study team members (Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, Project Management) to identify data integrity and subject safety risks;
  Escalate concerns as needed.
• Attend and present at Trusted Process meetings; participate in internal and external audits.
• Acquire basic understanding of ongoing protocol designs, disease terminology, and pathology.
• Adhere to data privacy guidelines, ICH, GCP, enterprise policies, SOPs, and project plans; comply with customer policies.
• May manage a small number of direct reports and participate in interviews.

Over the past five years, we have worked with 94% of all novel FDA‑approved drugs, 95% of EMA‑authorized products, and more than 200 studies across 73,000 sites and 675,000+ trial patients.

Partner with the Medical Director to provide clinical and scientific input to early and late‑stage clinical development programs, focusing on protocol‑specific requirements and ensuring scientific integrity and data quality of clinical trials. Collaborate with team members on data reviews and other medical management activities to ensure successful execution and conduct of clinical trials.

Tasks, duties, and responsibilities listed are not exhaustive. The Company reserves the right to assign additional tasks, duties, or job responsibilities. Equivalent experience, skills, and/or education will be considered for qualification assessment.

Phone:
Fax:
Toll-Free:

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender identity, sexual orientation, protected veteran status, disability, or any other legally protected status and will not be discriminated against.

For applicants requiring a reasonable accommodation due to a disability to complete any part of the application process, please contact us at  and one of our staff members will provide alternate means to submit your application.