Sr Medical Scientist

Updated: September 16, 2025Location: CAN-RemoteJob ID:25101747 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. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Job Responsibilities Works with the Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan) and engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input. Provides 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 of core activities. Performs regular and ad‑hoc medical review of data listings and data visualization; analyzes data to identify risks and data patterns/trends and supports documentation of medical reviews. Pro‑actively resolves medical data review issues as they arise. Authors medical data queries and reviews query responses, approving query closure in association with the Medical Director. May assist the Medical Director in patient profile review, scientific review of other study‑level data, protocol deviation review, and creation of Medical Review Summary reports as needed. Partners with Medical Directors for medical data review meetings and safety review meetings, including slide preparation as needed. Identifies issues in a timely manner, leads implementation of solutions, and/or escalates as appropriate; provides operational input on tactical implementation of studies in a global environment. Manages project scope of work, objectives, and quality of deliverables to ensure project milestones and timelines are met; serves as the primary interface between internal team, customers, and vendors for medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management to identify risks related to data integrity and subject safety, and escalates concerns to project leads in a timely manner. Attends and presents at Trusted Process meetings and may participate in internal and external audits. Acquires basic understanding and knowledge of ongoing protocol designs and disease‑related terminology and pathology. Adheres to all data privacy guidelines, ICH, and GCPs, as well as enterprise policies, SOPs, work instructions, and project plans; also adheres to customer policies and SOPs as required. May manage a limited number of direct reports and may participate in or conduct interviews. Get to Know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across 73,000 sites and 675,000+ trial patients. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Partners with Medical Director to provide clinical and scientific input to early and late‑stage clinical development programs with an emphasis on protocol‑specific requirements and ensuring the scientific integrity and data quality of clinical trials by using scientific knowledge. Collaborates with Medical Director(s) and other team members on data reviews and other Medical Management activities to ensure the successful execution and conduct of clinical trials. Phone: 919 876 9300Fax: 919 876 9360Toll-Free: 866 462 7373 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, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at: Email: jobs@syneoshealth.com. One of our staff members will work with you to provide alternate means to submit your application. #J-18808-Ljbffr