What are the responsibilities and job description for the Clinical Trial Liaison - Cardiovascular position at TSP (A Syneos Health Company)?
Location: Princeton, NJ, United States
Date Updated: Oct 2, 2025
Job ID: 11745-OTHLOC-CjawYfwH
Description
Clinical Trial Liaison, Philadelphia, PA (Cardiovascular)
The Clinical Trial Liaison with deep therapeutic and scientific knowledge, with strategic agility to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies in existing and new therapeutic areas. Will build strong relationships that improve return on enrollment while also partnering closely with Clinical Development and Medical Affairs teams to help shape development strategies.
Primary Responsibilities:
- Accountable for investigator engagement from identification and qualification through enrollment while supporting database lock and study closeout
- Serve as a scientific ambassador while providing a scientific rationale for patient eligibility requirements
- Influence enrollment through tailored recruitment strategies aligned with site capabilities
- Lead site-level strategy and risk planning while leveraging performance metrics as needed
- Drive inspection readiness
- Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
- Provide monitoring oversight and quality assurance for vendors
- Enable investigator experience by being a responsive, knowledgeable, and valued partner
- Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery)
Minimum Qualification Requirements:
- Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields
- 5 years of experience in clinical research or the pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites
- 3 years of experience working in the Cardiovascular therapeutic area
- Seeking candidates who reside in or who are able to relocate to Philadelphia, PA
Other Information/Additional Preferences:
- Advanced degree in a scientific or clinical field (PharmD, PhD, MD, or MSc preferred)
- Excellent understanding of GCP, clinical development, and operations, and trial lifecycle
- Data-driven decision-making skills
- Strong communication, negotiation, and organizational skills
Travel Requirements:
- Willingness to travel extensively, up to 80%
