Dir, Epidemiology Pipeline (TA-Oncology)

Dir, Epidemiology Pipeline (TA-Oncology) Updated: Yesterday Location: Morrisville, NC, United States Job ID: 25107866-OTHLOC-1500-2DID-2DR Job Responsibilities SME in Oncology Clinical Trials – serves as a scientific resource for RWLP management, company senior management, and other functions within the company providing expertise in multiple scientific areas. Works hand‑in‑hand with RWLP management, business development and operations personnel to develop and win global business opportunities; helps to lead the development and delivery of project proposals, bid defenses, and represents capabilities presentations. Provides overall scientific oversight of selected projects, responsible for meeting or exceeding customer expectations for timelines, budgets, quality, and overall satisfaction. Coordinates with the project manager to oversee the scientific aspects of study start‑up and ongoing study management. Leads the development of and/or peer‑review essential study documents including the protocol, case report forms, statistical analysis plan, study management plans, and interim/final study reports. Facilitates scientific advisory boards for safety studies and produces scientific reports, manuscripts, abstracts and presentations. Maintains a strong working understanding of clinical and epidemiological practice guidelines, clinical research models, protocol designs, real‑world research development trends, regulatory expectations, and develops trainings for RWLP/Company organization to enhance familiarity of epidemiologic study designs and applicable guidelines. Responsible for continued building of organizational capacity, improvement of scientific and operational processes and methodologies for non‑traditional site management tasks (remote or central monitoring approaches, minimized regulatory document collection, etc.), integrated RWLP technology solutions including secondary database resources, and RWLP Standard Operating Procedures (SOP) development and maintenance. Works collaboratively across the organization to help develop business opportunities in the area of post‑marketing safety commitments and/or risk management; develops and recommends techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state‑of‑the‑art practices. Works to develop collegial relationships with sponsors, thought‑leaders and clinical investigators. Develops abstracts, provides podium presentations, and leads authorship of articles, manuscripts, etc. in industry and peer‑reviewed journals to promote Company services. Requirements Graduate degree in Epidemiology, Statistics or Public Health (Master’s preferred; Doctorate preferred). In‑depth knowledge and experience with a variety of study designs, familiarity with post‑marketing and late‑phase study designs as well as relevant guidelines. Basic knowledge of statistical programming languages (e.g., SAS, R, Python). Excellent written and spoken communication, presentation skills. Strong personal communication and team‑oriented skills. Demonstrated leadership and technical skills. Benefits The benefits for this position may include a company car or car allowance, health benefits to include medical, dental and vision, company match 401k, eligibility to participate in employee stock purchase plan, eligibility to earn commissions or bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Equal Employment Opportunity Equity, diversity, and inclusion are core values. We are committed to compliance with the Americans with Disabilities Act, including provision of reasonable accommodations when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr