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Research Scientist – Epidemiology, Scientific Affairs

100% Remote Full-time Open now

Job Description:

  • Design and implement de novo data collection studies (retrospective, prospective, and/or cross-sectional), primarily for pregnancy safety studies
  • Conceptualize advanced study designs, supervise the development of study protocols, study reports, and other scientific deliverables
  • Review statistical analysis plans
  • Ensure project completion and quality delivery
  • Work closely with other scientists, oversight directors, project leads, biostatisticians, and programmers
  • Lead interactions with clients in the pharmaceutical and medical device industries
  • Review and finalize project deliverables ensuring validity and reliability of study findings
  • Oversee budget, deliverables, and project timelines; identify scope expansion and need for amendments
  • Contribute to thought leadership, such as abstracts and manuscripts as co-author and, when possible, first author
  • Serve as a consultant to other principal investigators or staff on other projects
  • Guide and mentor staff across multiple levels
  • Participate in proposals, design conceptual approaches for proposals, supervise and mentor junior staff, contribute to business development, and identify and pursue business opportunities within Evidera/PPD

Requirements:

  • PhD in epidemiology or a closely related field, or MSc with at least 5-7 years of relevant experience
  • Minimum 5+ years of consulting experience (or equivalent) preferred; 3-5 years of management experience preferred
  • Experience with peri- or post-approval late phase interventional studies and pregnancy/lactation studies is preferred
  • Broad experience in quantitative methods in real-world evidence and health services research, with the focus on design of non-interventional studies and data analysis using observational retrospective and prospective data
  • Strong understanding of relevant methodology and biostatistics
  • Knowledge of drug development process and international regulatory requirements
  • Proficient in MS Office; ability to read and understand SAS/STATA output; working knowledge of data analysis software (e.g., SAS, Stata, R) is a plus
  • Excellent written and verbal communication skills in English

Benefits:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

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