Dir, Epidemiology Pipeline (TA-Oncology)
A leading biopharmaceutical solutions organization.
Job Responsibilities
* Serve as a subject matter expert in oncology clinical trials.
* Act as a scientific resource for real‑world learning and pipeline (RWLP) management, senior company management, and other functions within the company, providing expertise in multiple scientific areas.
* Collaborate with RWLP management, business development, and operations personnel to develop and win global business opportunities; aid in the development and delivery of project proposals, bid defenses, and represent capabilities through presentations.
* Provide overall scientific oversight of selected projects, ensuring customer expectations for timelines, budgets, quality, and satisfaction are met or exceeded.
* Coordinate with the project manager to oversee the scientific aspects of study start‑up and ongoing study management; lead the development or peer‑review of essential study documents including protocols, case report forms, statistical analysis plans, study management plans, and interim/final study reports.
* Facilitate scientific advisory boards for safety studies and produce scientific reports, manuscripts, abstracts, and presentations.
* Maintain a strong working knowledge of clinical and epidemiological practice guidelines, research models, protocol designs, real‑world research development trends, regulatory expectations, and develop training for the organization.
* Responsible for building organizational capacity and improving scientific and operational processes for non‑traditional site management tasks, RWLP technology solutions, and standard operating procedures.
* Collaborate across the organization to create business opportunities in post‑marketing safety commitments and risk management; recommend techniques to improve productivity, efficiency, and cost‑effectiveness.
* Develop collegial relationships with sponsors, thought leaders, and clinical investigators.
* Develop abstracts, give podium presentations, and lead authorship of articles, manuscripts, and other industry publications to promote the company’s services.
Qualifications
* Subject matter expert in oncology clinical trials.
* Graduate degree in Epidemiology, Statistics, or Public Health (Master’s; Doctorate preferred).
* In‑depth knowledge and experience with a variety of study designs; familiarity with post‑marketing and late‑phase study designs and relevant guidelines.
* Basic knowledge of statistical programming languages (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
The benefits for this position may include a company car or car allowance, health benefits (medical, dental, and vision), a 401(k) company match, eligibility to participate in an employee stock purchase plan, eligibility to earn commissions or bonuses based on company and individual performance, and flexible paid time off and sick time.
Salary Range
The base salary range represents the anticipated low and high of the organization’s salary range for this position. Actual salary will vary based on factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Equal Employment Opportunity Statement
All qualified applicants will receive equal consideration for employment without regard to race, color, religion, national origin, gender, disability, veteran status, or applicable protected characteristics. No employee or applicant is to be discriminated against in any manner. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations where appropriate.
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