Dir, Epidemiology Pipeline (TA-Oncology)

Dir, Epidemiology Pipeline (TA-Oncology) Job Responsibilities Serve as scientific resource for RWLP management, company senior management, and other functions within the company providing expertise in multiple scientific areas. Work hand‑in‑hand with RWLP management, business development, and operations personnel to develop and win global business opportunities; lead development and delivery of project proposals, bid defenses, and presentations. Provide overall scientific oversight of selected projects, ensuring meeting or exceeding customer expectations for timelines, budgets, quality, and overall satisfaction. Coordinate with the project manager to oversee scientific aspects of study start‑up and ongoing study management, lead development and peer‑review of essential study documents including protocol, case report forms, statistical analysis plan, study management plans, interim/final study reports; facilitate scientific advisory boards and produce scientific reports, manuscripts, abstracts, and presentations. Maintain understanding of clinical and epidemiological practice guidelines, clinical research models, protocol designs, real‑world research development trends, regulatory expectations, and develop trainings for the organization on epidemiologic study designs and applicable guidelines. Build organizational capacity, improve scientific and operational processes and methodologies for non‑traditional site management tasks, integrated technology solutions, and standard operating procedures. Collaborate across the organization to develop business opportunities in post‑marketing safety commitments and risk management; recommend techniques to improve productivity, increase efficiency, reduce costs, and maintain best practices. Establish collegial relationships with sponsors, thought leaders, and clinical investigators. Develop abstracts, provide podium presentations, and lead authorship of articles, manuscripts, and other publications in industry and peer‑reviewed journals to promote company services. Requirements SME in oncology clinical trials. Graduate degree in Epidemiology, Statistics, or Public Health (Master’s required, Doctorate preferred). In‑depth knowledge of various study designs; familiarity with post‑marketing and late‑phase study designs and relevant guidelines. Basic knowledge of statistical programming language(s) (e.g., SAS, R, Python). Excellent written and spoken communication and presentation skills. Strong personal communication and team‑oriented skills. Demonstrated leadership and technical skills. Benefits and Salary The salary range for this position is subject to variation based on qualifications, skills, and proficiency. Benefits may include a company car or car allowance, health benefits (medical, dental, vision), 401(k) with company match, eligibility for an employee stock purchase plan, commission or bonus opportunities, and flexible paid time off (PTO) and sick time. At Syneos Health, we comply with all applicable federal, state, and municipal equal‑opportunity and anti‑discrimination laws. We are committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate. #J-18808-Ljbffr Syneos Health/ inVentiv Health Commercial LLC