<p>About the Opportunity</p> <p>We are seeking a highly skilled and experienced Clinical Trial Liaison to join</p> <p>our team. The ideal candidate will have a minimum of 3 years of experience</p> <p>in clinical research, a background in nursing or other healthcare fields, and a proven</p> <p>track record in patient recruitment. This role will involve working closely with clinical</p> <p>sites to ensure the smooth execution of clinical trials, with a particular focus on</p> <p>cardiovascular and/or imaging studies. As a key point of contact between study sites</p> <p>and the sponsor, the Clinical Trial Liaison will be responsible for fostering strong</p> <p>relationships, ensuring protocol compliance, and supporting patient recruitment and</p> <p>retention efforts.</p> <p>Salary: $100,000 - $130,000 TTC*</p> <ul> <li>Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, </li></ul> <p>bonuses, etc.). We hire employees anywhere within the United States and account for geography when</p> <p>determining base salary.</p> <p>Responsibilities</p> <ul> <li>Serve as the primary liaison between the clinical trial sponsor and </li></ul> <p>participating sites, ensuring effective communication and collaboration.</p> <ul> <li>Support clinical sites in meeting patient recruitment goals by providing </li></ul> <p>guidance on strategies, tools, and resources.</p> <ul> <li>Monitor site performance and provide proactive support to resolve any </li></ul> <p>issues related to protocol compliance, patient recruitment, and data</p> <p>collection.</p> <ul> <li>Ensure that all site staff are trained and compliant with study protocols, </li></ul> <p>Good Clinical Practice (GCP) guidelines, and regulatory requirements.</p> <ul> <li>Collaborate with site staff to identify and overcome barriers to patient </li></ul> <p>recruitment and retention.</p> <ul> <li>Track site progress and prepare reports on site performance, recruitment </li></ul> <p>metrics, and study milestones.</p> <ul> <li>Conduct regular site visits, both remote and in-person, to provide hands-on </li></ul> <p>support and address any operational challenges.</p> <ul> <li>Work closely with cross-functional teams, including project management, regulatory affairs, and data management, to ensure seamless study </li></ul> <p>execution.</p> <ul> <li>Maintain a thorough understanding of cardiovascular disease, study </li></ul> <p>protocols, and the specific needs of the patient population</p> <p>Requirements</p> <ul> <li>Bachelor's degree in healthcare related field; </li><li>Minimum of 3 years of experience in clinical research, with a focus on site </li></ul> <p>management and patient recruitment.</p> <ul> <li>Experience working in cardiovascular and/or imaging clinical trials is highly </li></ul> <p>desirable.</p> <ul> <li>Strong knowledge of clinical trial protocols, GCP guidelines, and </li></ul> <p>regulatory requirements.</p> <ul> <li>Proven ability to work independently and manage multiple clinical sites </li></ul> <p>simultaneously.</p> <ul> <li>Excellent communication, organizational, and problem-solving skills. </li><li>Ability to build strong relationships with site staff and foster a </li></ul> <p>collaborative working environment.</p> <ul> <li>Flexibility to travel as required for site visits and meetings. </li></ul> <p>Preferred Qualifications</p> <ul> <li>Advanced degree in nursing, clinical research, or a related field. </li><li>Experience working with diverse patient populations in cardiovascular </li></ul> <p>studies.</p> <ul> <li>Certification in clinical research (e.g., CCRP , ACRP , SOCRA) is a plus </li></ul>