Research Scientist – Epidemiology, Scientific Affairs

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🌲 North Carolina, Massachusetts – Remote

🌲 North Carolina – Remote 🍂 Massachusetts – Remote

💵 $150k - $170k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧬 Research Scientist

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 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