Remote Principal Research Scientist, Clinical Development

Syneos Health, Inc.; United States; Remote; USD 80,000 - 140,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits

401k match

Employee Stock Purchase Plan

Commissions/bonus

PTO and sick time

Job summary

Syneos Health, Inc. is seeking a Principal Research Scientist for ONC - Clinical Development Scientist (Sponsor Dedicated/ Remote US).

The role centers on coordinating the development and validation of bioanalytical methods per client requests, within timelines, in a dynamic biopharma setting. You will apply trial design knowledge to protocols, contribute to CRFs and regulatory documentation, and support data outputs and scientific communication.

Qualifications

• PharmD or PhD with 3+ years in clinical research or clinical pharmacology in biopharma, healthcare, consulting, academia or related environment.
• MS with 6+ years’ relevant scientific and/or drug development experience.
• BS or RN with 8+ years’ relevant scientific and/or drug development experience.

Responsibilities

• Develops understanding of clinical trial design to support study concepts and protocols.
• Participates in protocol review meetings and contributes to design discussions.
• Assists in preparation of study protocols, amendments, investigator materials, and clinical trial documentation.
• Contributes to CRFs, Data Management Plans, and Statistical Analysis Plans under supervision.
• Supports responses to investigator inquiries on scientific and procedural aspects of studies.
• Assists in data outputs, study findings, manuscripts, and presentations.

Skills

Microsoft Word

Microsoft Excel

Analytical software

Education

PharmD or PhD

MS

BS or RN

Tools

Analytical software (e.g., Analyst)

Job description

Syneos Health, Inc. is seeking a Principal Research Scientist for ONC - Clinical Development Scientist (Sponsor Dedicated/ Remote US).

The role centers on coordinating the development and validation of bioanalytical methods per client requests, within timelines, in a dynamic biopharma setting. You will apply trial design knowledge to protocols, contribute to CRFs and regulatory documentation, and support data outputs and scientific communication.