Senior Research Associate - Epidemiology
Role Overview
The Senior Research Associate drafts scientific deliverables, interacts with clients, contributes to strategy under senior direction, and coordinates multiple projects.
The role carries scientific responsibility for designing and implementing de novo data-collection projects under oversight of more senior staff.
Key Skills for This Role
Full Job Posting
Role overview
The Senior Research Associate drafts scientific deliverables, interacts with clients, contributes to strategy under senior direction, and coordinates multiple projects.
The role carries scientific responsibility for designing and implementing de novo data-collection projects under oversight of more senior staff.
Scientific and project responsibilities
- Provide scientific guidance on methodological and operational aspects of project design and conduct.
- Lead or coordinate drafts of protocols, analysis plans, case report forms, survey questions, and reports for senior review.
- Engage with project sponsors, physicians, clinical sites, and other relevant contacts.
- Monitor project budget spend and manage scientific task and deliverable timelines.
- Serve as Principal Investigator on some client engagements, with final responsibility for budgets, deliverables, and timelines.
- Lead or coordinate development of abstracts and manuscripts.
Business and organizational responsibilities
- Support business development through proposal development, sales-cycle participation, conference attendance, and presentations.
- Collaborate with clinical operations, data management, biostatistics, and data analysts; contribute to training materials and process improvements.
- Participate in client calls, address questions about assigned work, and contribute to client or project strategy under senior direction.
- May supervise or mentor junior staff or interns.
- Travel nationally and internationally may be expected.
Education and experience
- A PhD in epidemiology or a closely related field, or an MSc with 3–5 years of relevant experience, is required.
- A good understanding of epidemiologic methodology is required.
- Consultancy and/or CRO experience is highly desirable, not mandatory.
- Experience with de novo data-collection field projects, particularly non-interventional designs, is preferred.
Skills and languages
- Fluency in spoken and written Mandarin Chinese is required.
- Effective written English communication and scientific documentation are expected.
- Working knowledge of MS Office is listed; SAS, Stata, or R knowledge is a plus.
- Strong organization, time management, prioritization, decision-making, communication, and interpersonal skills are expected.
- Formal presentation experience is mentioned.
Schedule
- Standard Monday-to-Friday work schedule.
Workplace
- The source location is Remote, GB; the posting's environmental-conditions field says Office.
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