Clinical Trial Liaison
New
C
CleerlyHealthcare
Virtual USFull-TimeMiddle
Salary100,000 - 116,000 USD per year
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Job Details
- Experience
- Minimum of 3 years of experience in clinical research
- Required Skills
- Problem SolvingOrganizational skills
Requirements
- Bachelor’s degree in healthcare related field
- Minimum of 3 years of experience in clinical research, with a focus on site management and patient recruitment.
- Experience working in cardiovascular and/or imaging clinical trials is highly desirable.
- Strong knowledge of clinical trial protocols, GCP guidelines, and regulatory requirements.
- Proven ability to work independently and manage multiple clinical sites at the same time.
- Excellent communication, organizational, and problem-solving skills.
- Ability to build strong relationships with site staff and foster a collaborative working environment.
- Flexibility to travel as required for site visits and meetings, travel up to 50% of time.
- Advanced degree in nursing, clinical research, or a related field.
- Experience working with diverse patient populations in cardiovascular studies.
- Certification in clinical research (e.g., CCRP, ACRP, SOCRA) is a plus
Responsibilities
- Serve as the primary liaison between the clinical trial sponsor and participating sites, ensuring effective communication and collaboration.
- Support clinical sites in meeting patient recruitment goals by providing guidance on strategies, tools, and resources.
- Monitor site performance and provide proactive support to resolve any issues related to protocol compliance, patient recruitment, and data collection.
- Ensure that all site staff are trained and compliant with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
- Collaborate with site staff to identify and overcome barriers to patient recruitment and retention.
- Track site progress and prepare reports on site performance, recruitment metrics, and study milestones.
- Conduct regular site visits, both remote and in-person, to provide hands-on support and address any operational challenges.
- Work closely with cross-functional teams, including project management, regulatory affairs, and data management, to ensure seamless study execution.
- Maintain a thorough understanding of cardiovascular disease, study protocols, and the specific needs of the patient population
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