Top 338 Scientific programmers Jobs

Research Scientist - Epidemiology and Scientific Affairs
Thermo Fisher Scientific —North Carolina
- $150,000 - $170,000 a year
- Full-time
- 5 years
- English
- Office
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Director Biostatistics
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CNC Programmer (Aerospace and Defense)
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Principal Biostatistician
CSL Behring —King of Prussia, PA
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Director, Statistical Programming
CSL Behring —King of Prussia, PA
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Penfield Search Partners —Philadelphia, PA
- 6 years
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Associate Director, Biostatistics
Genmab —Princeton, NJ
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Scientific Data Analyst
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2026 PhD Graduate - Senior Engineer-Analyst for ISR Scientific Applications
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Real Chemistry —Remote
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Research Scientist - Epidemiology and Scientific Affairs

Thermo Fisher Scientific -
North Carolina

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Job Details

Full-time
$150,000 - $170,000 a year

Benefits

Commuter assistance
Paid parental leave
Caregiver leave
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Statistics
Business development management
Healthcare consulting
Quantitative applied research
Clinical study protocols and reports
Biostatistics-based research
Scientific publications
Business development within consulting
SAS
Team leadership
5 years
Coaching
Client rapport building
Presentations for conferences or internal meetings
R
Doctoral degree in epidemiology
English
Microsoft Office
SAS language
Stata
Research project design
Collaborative research
Team development
Research project technical leadership
Professional development support
Presentation skills
Epidemiological study projects
Doctor of Philosophy
Content creation for professionals
Task prioritization

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

The Real-World Science, Epidemiology and Scientific Affairs team focuses on generating real-world evidence and supports biopharmaceutical companies throughout the product lifecycle, from early pre-launch planning to launch, and post-marketing management. Our focus is on helping our clients in the pharmaceutical/ biotechnology/ medical device industries generate real-world evidence to demonstrate and support the value of their products. Through the generation of real-world data via the design, implementation, and analyses of observational/non-interventional studies, we may provide key information such as:

Pregnancy safety studies (e.g., pregnancy exposure registries, descriptive pregnancy safety studies)
Incidence and prevalence of diseases and co-morbidities, and their risk factors
Burden of disease, unmet needs
Treatment patterns and drug utilization
Healthcare resource utilization
Overall safety, incidence of adverse events of special interest
Effectiveness and comparative effectiveness data

This position will focus on pregnancy safety studies.

Position Overview

The Research Scientist takes the role of independent principal investigator/consultant of projects and is responsible for coordinating all aspects of project delivery, including delegating project management tasks to junior staff. This role will also take scientific responsibility for project completion, strategic consultation, and for use of the best methods to address research needs. This position will focus primarily on implementing pregnancy safety studies.

Essential Duties (other duties may be assigned)

Scientific Accountability: 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.
Collaboration: Work closely with other scientists, oversight directors, project leads, biostatisticians, and programmers.
Client Engagement: Lead interactions with clients in the pharmaceutical and medical device industries.
Deliverables: Review and finalize project deliverables ensuring validity and reliability of study findings.
Project Management: Oversee budget, deliverables, and project timelines; identify scope expansion and need for amendments.
Thought leadership/Publications: Contribute to thought leadership, such as abstracts and manuscripts as co-author and, when possible, first author.
Consultation: Serve as a consultant to other principal investigators or staff on other projects.
Mentorship: Guide and mentor staff across multiple levels.
Growth: Lead the growth in your area of responsibility. 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.
Travel: National and international travel is expected.
Management: Possible managerial duties, including actively managing and/or mentoring a team of scientists.
Participate in client calls and address questions about your work.
Proactively identify issues and develop strategies for mitigation and/or effective solutions.
Provide scientific consultation and use the best methods to address research needs.
Contribute to strategic thinking and innovation.

Education, Professional Skills and Experience

Education: PhD in epidemiology or a closely related field, or MSc with at least 5-7 years of relevant experience. Degree in perinatal epidemiology, preferred.
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.
Knowledge: 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.
Technical Skills: 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.

Personal Skills & Competencies

Excellent written and verbal communication skills in English.
Strong organizational, time-management, prioritization, and decision-making skills.
Ability to learn and apply new information, skills, and procedures quickly.
Proactive and positive approach to tasks and projects.
Strong interpersonal skills with the ability to develop and sustain positive rapport with internal and external contacts.
Experience presenting ideas to individuals and groups.
Sound professional judgment in analyzing, responding to, and resolving enquiries, issues, and escalations.
Ability to tailor and deliver high-level presentations to diverse audiences.
Ability to make independent, critical decisions based on relevant information.
Desire and ability to guide and coach junior to mid-level scientific staff.

Why join us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Compensation and Benefits

The salary range estimated for this position based in North Carolina is $150,000.00–$170,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

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

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Apply Now

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