Job Description

About the Opportunity

We are seeking a highly skilled and experienced Clinical Trial Liaison to join
our team. The ideal candidate will have a minimum of 3 years of experience
in clinical research, a background in nursing or other healthcare fields, and a proven
track record in patient recruitment. This role will involve working closely with clinical
sites to ensure the smooth execution of clinical trials, with a particular focus on
cardiovascular and/or imaging studies. As a key point of contact between study sites
and the sponsor, the Clinical Trial Liaison will be responsible for fostering strong
relationships, ensuring protocol compliance, and supporting patient recruitment and
retention efforts.

 

Salary: $100,000 - $130,000 TTC*

*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission,
bonuses, etc.). We hire employees anywhere within the United States and account for geography when
determining base salary.

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

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
  simultaneously.
• 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.

 

Preferred Qualifications

• 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