Study Manager - Future Roles (us)

Syneos Health

Morrisville, NC, United States
On-site
Gcp and regulatory compliance
Client liaison and contractual agreement
Quality, timelines, and budget management
Manages interdisciplinary clinical research studies, ensuring compliance with GCP, SOPs, and regulatory requirements, acting as the primary liaison between the Company and the Customer

Job Summary

  • Manages interdisciplinary clinical research studies, ensuring compliance with GCP, SOPs, and regulatory requirements, acting as the primary liaison between the Company and the Customer.
  • Leads project teams to ensure quality, timelines, and budget management, holding accountability for financial performance and proactive issue management.
  • Syneos Health offers a supportive environment with career development, training, and a Total Self culture, along with benefits like a company car, health benefits, 401k match, ESPP, and flexible PTO.

Matching Summary

Manages interdisciplinary clinical research studies, ensuring compliance with GCP, SOPs, and regulatory requirements, acting as the primary liaison between the Company and the Customer.

Skills & Requirements

Must-have

  • GCP and regulatory compliance
  • Client liaison and contractual agreement
  • Quality, timelines, and budget management
  • Financial performance accountability
  • Study conduct partner coordination
  • TMF quality and completeness
  • Inspection readiness

Nice-to-have

  • Embrace new technologies
  • Develop strong client relationships
  • Participate in bid defense meetings
  • Line management experience

Key Requirements

  • Bachelor’s Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience
  • Clinical research organization (CRO) and relevant therapeutic experience preferred
  • Strong knowledge of Good Clinical Practice/ICH guidelines
  • Ability to travel as necessary (approximately 25%)

Work Rights

Not specified

Tailored Resume

Cover Letter