Remote Principal Research Scientist, Bioanalytical Methods

Syneos Health, Inc.; North Carolina; Remote; USD 80,000 - 140,000; Full time

Benefits offered by this job

Health benefits

401k match

Stock Purchase Plan

Bonuses/Commissions

Flexible PTO

Job summary

Syneos Health, Inc. seeks a Principal Research Scientist ONC - Clinical Development Scientist to coordinate and execute bioanalytical method development and validation projects for sponsor-delivered trials in a remote US setting.

You will collaborate with cross-functional teams to ensure timely, scientifically rigorous study deliverables. Requirements include advanced degrees in pharma/biomedicine with several years of clinical research or drug development experience, plus strong regulatory and

Qualifications

• PharmD or PhD with 3+ years in clinical research or 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 experience in scientific/drug development.

Responsibilities

• Coordinate and carry out development and validation of bioanalytical methods per client requests and timelines.
• Support protocol development and review, contributing to scientific rationale and study design.
• Assist in preparation of study protocols, amendments, investigator materials, manuals and other clinical documentation.
• Contribute to CRFs, Data Management Plans, and Statistical Analysis Plans with supervision.
• Support responses to investigator inquiries on scientific, clinical and procedural aspects.
• Assist in data outputs, study findings, manuscripts and scientific presentations.

Skills

Clinical research

English bilingual

Problem solving

Education

PharmD or PhD

MS with 6+ years

BS or RN with 8+ years

Job description

Syneos Health, Inc. seeks a Principal Research Scientist ONC - Clinical Development Scientist to coordinate and execute bioanalytical method development and validation projects for sponsor-delivered trials in a remote US setting.

You will collaborate with cross-functional teams to ensure timely, scientifically rigorous study deliverables. Requirements include advanced degrees in pharma/biomedicine with several years of clinical research or drug development experience, plus strong regulatory and