Description
Syneos Health is seeking experienced Clinical Project Managers with strong global immunology clinical trial experience to join a high-performing sponsor-dedicated team supporting a diverse portfolio of immunology studies across multiple indications and phases of development.
As a Clinical Project Manager II, you will help drive the operational execution and delivery of global immunology clinical trials, ensuring studies are conducted efficiently, compliantly, and according to established timelines.
Key Responsibilities:
- Support and partner with Clinical Study Leads and cross-functional study teams on global immunology trials
- Lead day-to-day study management activities across study startup, conduct, maintenance, and closeout
- Manage study timelines, deliverables, risks, and issue resolution
- Oversee external vendors, CROs, central laboratories, specialty providers, and other study partners
- Coordinate Clinical Team meetings and drive action item follow-up
- Support study-level planning, forecasting, and operational strategy execution
- Monitor study performance metrics and proactively identify areas requiring intervention
- Ensure inspection readiness and compliance with applicable regulations and sponsor requirements
- Collaborate with stakeholders across Clinical Operations, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, Safety, Supply Chain, and Quality
- Contribute to study status reporting and executive-level communications
- Support achievement of study milestones, enrollment targets, database locks, and study closeout activities
- Travel up to 25%
Required Qualifications:
- Bachelor's degree in a scientific, healthcare, or related field
- 3+ years of Clinical Project Management experience supporting global immunology clinical trials
- Experience managing studies across multiple countries and regions
- Vendor management experience required
- Strong understanding of clinical trial operations and study lifecycle management
- Experience supporting Phase I, Phase II, Phase III, and/or Phase IV immunology studies
- Strong working knowledge of ICH-GCP guidelines and clinical research regulations
- Proficiency with Microsoft Office Suite
- Ability to work effectively within global, cross-functional matrix organizations
Immuno-Oncology Therapeutic Area Experience:
- Candidates should have direct clinical trial experience supporting one or more immunology indications, including but not limited to:
- Gastroenterology / Inflammatory Bowel Disease (IBD)
- Autoimmune and Inflammatory Diseases
- Dermatology
- Respiratory and Allergy
- Other Immune-Mediated Disorders
Preferred Qualifications:
- Experience independently leading global immunology studies
- Experience supporting complex, multi-regional Phase II and Phase III programs
- Experience with early-phase immunology studies (Phase I/Ib)
- Experience supporting biologics, monoclonal antibodies, immunomodulators, or novel immune-targeted therapies
- Familiarity with CTMS, eTMF, IRT/RTSM, and clinical data review platforms
- Experience working in sponsor-dedicated or FSP environments
Benefits:
- Salary Range: $120,000–$135,000
- 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
- Health benefits to include Medical, Dental and Vision
- Company car or car allowance