Medical Director (HIV Research Scientific Lead - Clinical/Observational Research)

Medical Director (HIV Research Scientific Lead - Clinical/Observational Research) Updated: Yesterday Location: Morrisville, NC, United States Job ID: 25109760-OTHLOC-1500-2DDE-2DR Description Syneos Health® is a leading fully-integrated life sciences services organization that accelerates customer success across the drug development and commercialization continuum. The Clinical Solutions team applies extensive expertise to understand customer needs and shape solutions. Job Responsibilities Provides medical oversight of assigned clinical studies as a medical monitor and primary medical contact for customers. Provides medical input and oversight for Drug Safety and Pharmacovigilance. Responsible for protocol design and development; provides input into protocol amendments. Develops and delivers project‑specific and therapeutic training to project team members, clinical site staff, and customer staff as needed. Provides medical and therapeutic input to Study Start‑Up, Feasibility, and Subject Identification efforts, including review of Informed Consent Templates and subject‑facing materials. Provides input into data collection tools, monitoring plans, and review and analysis plans. Oversees assigned Medical Scientist staff and Medical Director colleagues in reviewing clinical data, presenting trends, issues, and mitigation strategies to customers and project teams to minimize risks to subject safety or data integrity. Provides after‑hours medical coverage for clinical studies. Adheres to enterprise policies, work instructions, standard operating procedures, and project plans, as well as customer policies and standard operating procedures as required. Maintains in‑depth knowledge of FDA and worldwide drug development regulations, national and ICH Good Clinical Practice (GCP) guidelines. May support responses to Requests for Proposals (RFPs) or Bid Defense Meetings (BDMs) upon request. May provide input to clinical development or regulatory teams within the Company upon request. May represent the Company at scientific meetings upon request. Qualifications Doctorate degree in medicine with clinical experience in the specific therapeutic area and required clinical research experience. Must possess in‑depth knowledge of FDA and worldwide drug development regulations. Expected to have a strong understanding of medical terminology and drug nomenclature across multiple nations. Experience working in matrix teams is preferred. Proficiency in Microsoft Office Suite, email, and voicemail. Excellent organizational, interpersonal, communication, and presentation skills. Attention to detail, accuracy, and ability to manage multiple tasks and deadlines in a dynamic environment are essential. Fluency in written and spoken English is required. Up to 25% travel may be required. Benefits Benefits for this position may include a company car or car allowance, medical, dental, and vision health benefits, 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 in accordance with applicable federal, state, and municipal requirements. Salary Range $146,000.00 - $277,000.00 Summary Provides medical oversight of assigned clinical studies, interacts with senior management, customers, and project teams to ensure subject safety and scientific integrity, delivers therapeutic area medical input and consultation, participates in business development and scientific meetings, and performs the duties of Medical Monitor. Additional Information Tasks, duties, and responsibilities are not exhaustive. The Company may assign other tasks at its discretion. Equivalent experience, skills, or education may be considered. The Company is committed to compliance with the Americans with Disabilities Act and provides reasonable accommodations when appropriate. • The Company complies with all applicable federal, state, and municipal paid sick time requirements. #J-18808-Ljbffr