Principal Research Scientist – Clinical Development

Syneos Health

Principal Research Scientist coordinating and validating bioanalytical methods for clinical development and collaborating closely with clinical and operational teams at Syneos Health.

Posted 7/31/2026full-timeRemote • 🇺🇸 United StatesLead💰 $79,800 - $139,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial design, bioanalytical method development, and regulatory compliance, with a strong ability to synthesize scientific literature and contribute to study documentation. Proficient in scientific problem solving and effective communication in both verbal and written formats.

Highest-signal resume keywords

Clinical Trial DesignBioanalytical Method DevelopmentRegulatory ComplianceScientific Problem SolvingMultiple Myeloma Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchDrug DevelopmentStatistical Analysis PlansData Management PlansCase Report FormsProtocol DevelopmentGood Clinical PracticeAnalytical SoftwareMicrosoft WordMicrosoft Excel

Soft Skills

CommunicationTeam CoordinationProblem Solving

Tools & Technologies

Microsoft OfficeAnalyst Software

Certifications & Qualifications

PharmDPhDMSBSRN

Industry Keywords

BiopharmaHealthcareConsultingAcademiaCAR-T Therapy

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Responsible for coordinating and carrying out the full spectrum of activities related to the development and validation of bioanalytical methods according to client requests and within the required timeframes
Develops a solid understanding of clinical trial design and applies this knowledge to support the creation of study concept documents and clinical protocols
Participates in protocol review meetings, contributing to discussions on scientific rationale and operational study design considerations
Assists in the preparation of study protocols, protocol amendments, investigator meeting materials, study manuals, and other clinical trial documentation under appropriate guidance
Contributes to the development of Case Report Forms (CRFs), Data Management Plans, and Statistical Analysis Plans with supervision
Supports responses to investigator inquiries related to scientific, clinical, and procedural aspects of studies
Assists in the preparation and review of data outputs, summary reports, study findings, manuscripts, and scientific presentations
Provides support in the development and review of regulatory submission documents
Identifies and helps address moderately complex study-related challenges, implementing solutions with guidance from experienced team members
May coordinate project teams and provide direction on assigned activities when required
May perform clinical monitoring responsibilities for individual studies or specific components of larger clinical programs
Demonstrates the ability to quickly learn new therapeutic areas and synthesize relevant scientific literature to support study development activities
Ensures compliance with applicable regulatory requirements, Good Clinical Practice (GCP) guidelines, and company Standard Operating Procedures (SOPs).

Requirements

What you’ll need

PharmD or PhD with 3+ years in clinical research or clinical pharmacology with scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a 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
Relevant experience in Multiple Myeloma and/or CAR-T Therapy is preferred
Experienced with Microsoft Office and other job-related programs
Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel and analytical software (E.g. Analyst)
Demonstrates skills in scientific problem solving
English level: Required bilingualism includes communicating verbally and in writing on topics that are often technical, and writing procedures or technical reports.

Benefits

Comp & perks

Health benefits to include Medical, Dental and Vision
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO) and sick time