Syneos Health Careers: Apply Now for Clinical Scientist Role
Syneos Health Careers: Syneos Health, a global biopharmaceutical solutions organization, is hiring an FSP Clinical Scientist to support early- and late-stage clinical development programs. This role is ideal for life science and medical professionals seeking to work at the intersection of clinical research, medical data review, and scientific strategy, contributing directly to the integrity and success of global clinical trials.
Syneos Health Careers: Job Details
- Position: FSP Clinical Scientist
- Employment Type: Full-time
- Work Model: Functional Service Provider (FSP)
- Industry: Clinical Research / Biopharmaceutical
- Therapy Area: Hematology (anticipated focus on Myeloma or Lymphoma)
- Experience Level: Experienced Clinical Research Professional
About the Company
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, partnering with customers to accelerate the delivery of therapies that change lives. With over 29,000 employees across 110 countries, Syneos Health supports clinical development, medical affairs, and commercial solutions across the drug development lifecycle.
Over the past five years, Syneos Health has worked on 94% of novel FDA-approved drugs and 95% of EMA-authorized products and conducted more than 200 studies across 73,000 sites, impacting 675,000+ trial patients globally. The organization is driven by innovation, agility, and a strong commitment to patient-centric research.
Syneos Health Careers: Qualifications
- Degree (MSc, PharmD, PhD, DMD, MD) or equivalent
- Relevant scientific or clinical research experience
- Strong understanding of clinical trial processes and medical data analysis
- Knowledge of ICH-GCP guidelines and drug development preferred
- Excellent written and verbal communication skills
- Strong organizational and time-management abilities
- Proficiency in MS Office (Word, Excel, PowerPoint)
- Ability to work effectively in a cross-functional, global team environment
- Self-starter comfortable with dynamic timelines and changing scopes
About the Role
The FSP clinical scientist partners closely with the medical director to provide clinical and scientific input across early- and late-stage clinical trials. The primary focus of this role is medical and scientific data review, ensuring data integrity, subject safety, and regulatory compliance. The role involves collaboration with cross-functional teams and supports critical medical management activities throughout the study lifecycle.
Key Responsibilities
- Perform medical and scientific data review for hematology clinical trials
- Conduct standard data listing reviews (AEs, concomitant medications, efficacy, and safety data)
- Support patient profile reviews, safety narratives, PD analysis, and efficacy assessments
- Collaborate with the Medical Director to develop Medical Management, Data Review, and Eligibility Review Plans
- Author medical data queries and review query responses
- Participate in safety review meetings and medical data review discussions
- Support documentation, including Medical Review Summary reports
- Interface with internal teams, customers, and vendors for medical data review activities
- Identify risks, data trends, and patterns affecting subject safety or data integrity
- Collaborate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams
- Ensure compliance with ICH, GCP, data privacy regulations, and company SOPs
- Participate in internal and external audits as required
