Clinical Scientist - Vaccine

Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. Performs regular and ad‑hoc medical review of data listings and data visualization, analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. Assists Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. Manages project scope of work, objectives, and quality of deliverables to ensure the project‑specific milestones and timelines are met; serves as primary interface between internal team, customers, and vendors in medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management to identify risks related to data integrity and subject safety; escalates ongoing and newly developed study concerns. Attends 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, GCP, enterprise policies, SOPs, work instructions, and project plans; and adheres to customer policies as required. Summary Partners with Medical Director to provide clinical and scientific input to early and late‑stage clinical development programs, ensuring the scientific integrity and data quality of clinical trials by using scientific knowledge. Collaborates with Medical Directors and other team members on data reviews and other medical management activities to ensure successful execution of clinical trials. Benefits Benefits for this position may include a company car or car allowance, health benefits (Medical, Dental, Vision), company match 401(k), eligibility to participate in an Employee Stock Purchase Plan, eligibility to earn commissions/bonuses based on company and individual performance, and flexible paid time off (PTO) and sick time. Eligibility for paid sick time may vary depending on location. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Legal and EEO Statement 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. 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. The Company also complies with the EU Equality Directive and other applicable laws. #J-18808-Ljbffr Syneos Health, Inc.