Vaccine Study Project Lead

Syneos Health/ inVentiv Health Commercial LLC; Morrisville (NC); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Car allowance

Health benefits

401k match

Stock purchase plan

Bonus eligibility

PTO & sick leave

Job summary

Syneos Health is seeking a Study Manager for Vaccine programs to oversee interdisciplinary clinical research studies, ensuring GCP compliance and alignment with contractual obligations. You will coordinate study teams, manage timelines and budgets, and maintain TMF quality across projects.

The role requires strong communication, organizational excellence and approximately 25% travel, with opportunities to influence study delivery and client satisfaction within a global biopharma solutions

Qualifications

• Bachelor's Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience.
• CRO experience and therapeutic knowledge preferred with strong knowledge of GCP/ICH guidelines.
• Strong organizational skills and ability to manage time independently.
• Ability to travel approximately 25%.
• Excellent communication, presentation and interpersonal skills.

Responsibilities

• Project leadership and delivery; oversee interdisciplinary clinical research studies in compliance with GCP and regulatory requirements.
• Serve as primary liaison betweenCompany and Customer to ensure timely study launch, conduct and closeout.
• Lead project team to ensure quality, timelines and budget management.
• Accountable for the financial performance of each project and coordination of study partners.

Skills

Organizational skills

Time management

Communication

Interpersonal skills

Travel flexibility

Education

Bachelor's degree in life sciences/Medicine/Pharmacy/Nursing

Job description

Syneos Health is seeking a Study Manager for Vaccine programs to oversee interdisciplinary clinical research studies, ensuring GCP compliance and alignment with contractual obligations. You will coordinate study teams, manage timelines and budgets, and maintain TMF quality across projects.

The role requires strong communication, organizational excellence and approximately 25% travel, with opportunities to influence study delivery and client satisfaction within a global biopharma solutions