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Senior Research Associate - Epidemiology

Thermo Fisher Scientific
Remote, GBR
Full-time
Senior
Remote
Discovered 2 weeks ago
EpidemiologyEpidemiologic methodologyObservational study designDe novo data collectionScientific protocol developmentAnalysis plan development

Full Job Posting

Schedule

  • Standard Monday-to-Friday work schedule.

Workplace

  • The job data lists the role as remote in the United Kingdom.
  • The description lists office environmental conditions.
  • National and international travel may be expected.

Role overview

Draft scientific protocols, reports, and project deliverables, engage with clients, and contribute to strategy under senior staff direction.

Lead scientific coordination and project management, including scope, progress tracking, and coordination of tasks across multiple projects.

Work under oversight of more senior staff, with possible Principal Investigator responsibility on some engagements.

Duties

  • Design and implement retrospective, prospective, and/or cross-sectional de novo data collection projects.
  • Advise on scientific methodology and operational considerations for project design and conduct.
  • Lead or coordinate draft protocols, analysis plans, case report forms, survey questions, and reports for senior review.
  • Engage with sponsors, physicians, clinical sites, and other relevant contacts.
  • Monitor project budget spend and scientific task and deliverable timelines.
  • On some engagements, serve as Principal Investigator with final responsibility for budget, deliverables, and timelines.
  • Develop abstracts and manuscripts; support proposals, sales-cycle activities, conferences, and presentations.
  • Support mentoring, collaboration with clinical operations and data teams, training materials, and process improvement.
  • Participate in client calls, answer questions about own work, and contribute to client and project strategy under senior direction.

Education and experience

  • PhD in epidemiology or a closely related field, or MSc with 3–5 years of relevant experience, is required.
  • Good understanding of epidemiologic methodology is required.
  • Consultancy and/or CRO experience is highly desirable.
  • De novo data collection field-project experience, particularly non-interventional designs, is preferred.
  • Experience designing peri- or post-approval late-phase interventional projects is a plus, but is not required.

Professional skills

  • Working knowledge of MS Office is required; knowledge of data-analysis software such as SAS, Stata, or R is a plus.
  • Fluent spoken and written Mandarin Chinese is required.
  • Effective written English is needed for scientific reports, presentations, emails, and other deliverables.
  • The role calls for strong organization, time management, prioritization, decision-making, communication, interpersonal skills, and formal presentation experience.
  • The role requires the ability to learn quickly, remain proactive, and adapt to project, budget, process, or client changes.

Consulting and team expectations

Deliver a positive client experience, listen to client needs, recommend solutions, and use sound judgment to respond to inquiries and escalations.

May mentor or manage junior staff or practice-area interns.

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