Dir, Epidemiology Pipeline (TA-Oncology)
Updated: Today
Location: London, LND, United Kingdom
Job ID:25107866-OTHLOC-3526-2DR
Seeking a subject‑matter expert in oncology clinical trials to serve as a scientific resource for the organization’s real‑world evidence pipeline (RWLP) and senior management.
Job Responsibilities
* Serve as a scientific resource for Real‑World Evidence pipeline management, senior management, and other internal functions, 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; help lead development and delivery of project proposals, bid defenses, and represent capabilities presentations.
* Provide overall scientific oversight of selected projects, responsible for 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 of study documents (protocol, case report forms, statistical analysis plan, study management plans, interim/final reports); facilitate scientific advisory boards and produce scientific reports, manuscripts, abstracts, presentations.
* Maintain a strong working understanding of clinical and epidemiological practice guidelines, protocol designs, real‑world research development trends, regulatory expectations, and develop trainings for the organization to enhance familiarization of epidemiologic study designs and applicable guidelines.
* Build organizational capacity, improve scientific and operational processes and methodologies for non‑traditional site management tasks (remote or central monitoring, minimized regulatory document collection, etc.), integrated RWLP technology solutions, and SOP development and maintenance.
* Work collaboratively across the organization to develop business opportunities in post‑marketing safety commitments and/or risk management; recommend techniques to improve productivity, increase efficiencies, cut costs, and maintain state‑of‑the‑art practices.
* Build collegial relationships with sponsors, thought leaders, and clinical investigators.
* Develop abstracts, lead podium presentations, and lead authorship of articles and manuscripts for industry and peer‑reviewed journals to promote company services.
Requirements
* Subject‑matter expert in Oncology Clinical Trials.
* Graduate degree in Epidemiology, Statistics, or Public Health (Master’s preferred; Doctorate preferred).
* In‑depth knowledge of and experience with multiple study designs; familiarity with post‑marketing and late‑phase designs and relevant guidelines preferred.
* Basic knowledge of statistical programming languages (e.g., SAS, R, Python).
* Excellent written and oral communication, presentation skills.
* Strong personal communication and team‑oriented skills.
* Demonstrated leadership and technical skills.
Salary Range
The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Benefits
* Company car or car allowance.
* Health benefits: Medical, Dental and Vision.
* Company match 401(k).
* Eligibility to participate in Employee Stock Purchase Plan.
* Eligibility to earn commissions/bonus based on company and individual performance.
* Flexible paid time off (PTO) and sick time; eligibility for paid sick time may vary depending on location. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. Further, nothing contained herein should be construed to create an employment contract.
Equal Opportunity Employer
The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate, to assist employees or applicants to perform the essential functions of the job. The Company also complies with the EU Equality Directive and applicable legislation in each country in which it operates, and it is committed to a diverse, equitable and inclusive culture.
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