Dir, Epidemiology Pipeline (TA-Oncology)

Dir, Epidemiology Pipeline (TA-Oncology)

We are seeking a subject matter expert in oncology clinical trials who will provide scientific oversight and support for real‑world studies and global business opportunities. This position is part of an ongoing talent pipeline; there is no immediate opening, but qualified candidates will be considered when opportunities arise.

Job Responsibilities

• Serve as a scientific resource for real‑world studies, company senior management, and other functions by providing expertise in multiple scientific areas.
• Work hand‑in‑hand with management, business development, and operations to develop and win global business opportunities; lead project proposals, bid defenses, and represent capabilities in presentations.
• Provide overall scientific oversight of selected projects to meet or exceed customer expectations for timelines, budgets, quality, and 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, and interim/final study reports. Facilitate scientific advisory boards and produce scientific reports, manuscripts, abstracts, and presentations.
• Maintain a strong understanding of clinical and epidemiological practice guidelines, research models, protocol designs, real‑world research trends, and regulatory expectations. Develop trainings to enhance organization’s familiarity with epidemiologic study designs and applicable guidelines.
• Build organizational capacity and improve scientific and operational processes for non‑traditional site management tasks (remote or central monitoring, minimized regulatory document collection) and integrated technology solutions. Develop and maintain standard operating procedures.
• Collaborate across the organization to develop business opportunities in post‑marketing safety commitments and risk management. Recommend techniques to improve productivity, efficiency, reduce costs, and maintain state‑of‑the‑art practices.
• Build collegial relationships with sponsors, thought leaders, and clinical investigators.
• Develop abstracts, deliver podium presentations, and lead authorship of articles, manuscripts, and other publications to promote company services.

Qualifications

• Subject‑matter expert in oncology clinical trials.
• Graduate degree in Epidemiology, Statistics, or Public Health (Master’s preferred, Doctorate preferred).
• In‑depth knowledge and experience with a variety of study designs, including post‑marketing and late‑phase studies. Familiarity with relevant guidelines is preferred.
• Basic knowledge of statistical programming languages such as SAS, R, or Python.
• Excellent written and verbal communication and presentation skills.
• Strong interpersonal and team‑oriented skills.
• Demonstrated leadership and technical skills.

Benefits

Potential benefits may include a company car or car allowance, health benefits (medical, dental, vision), company‑match 401(k), participation in the employee stock purchase plan, eligibility for commissions/bonuses, and flexible paid time off (PTO) and sick time.

Additional Information

Tasks, duties, and responsibilities as listed may not be exhaustive. The company may assign additional duties at its discretion. The company complies with all applicable laws regarding equal opportunity and accommodations for qualified individuals with disabilities.