Offer summary

Qualifications:

Bachelor's degree in a relevant field such as life sciences, nursing, or healthcare management., Proven experience in clinical research and site relationship management., Excellent communication and interpersonal skills are essential., Strong organizational and project management skills with a solid understanding of GCP and regulatory requirements..

Key responsibilities:

Develop and maintain strong relationships with key personnel at clinical trial sites.

Serve as a liaison between the sponsor and clinical trial sites, ensuring clear communication of study protocols.

Conduct Monitoring Oversight Visits and regular site engagement activities to ensure high-quality trial execution.

Track and report site engagement activities, enrollment status, and performance metrics.

Job description

TFS HealthScience is a leading mid-sized Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. Our Clinical Operations team, led by industry experts, combines the full-service capabilities and global reach of a large CRO with the flexibility and personal approach of a mid-sized CRO.

As a member of our SRS team, you will be fully dedicated to a single sponsor based in the United States. This is a contract-based position.

Responsibilities:

Relationship Building: Develop and maintain strong relationships with key personnel at clinical trial sites, including principal investigators, site coordinators, and other site staff.
Liaison Role: Serve as a bridge between the sponsor and clinical trial sites, ensuring clear and timely communication of study protocols, updates, and key information.
Site Oversight: Conduct Monitoring Oversight Visits and regular site engagement activities to ensure high-quality trial execution.
Enrollment Support: Design customized site-level engagement plans to help drive enrollment and support timely patient recruitment.
Issue Resolution: Collaborate with CRO CRAs and Medical Science Liaisons to identify, mitigate and resolve site-level challenges.
Feasibility Support: Participate in feasibility and site qualification visits, collaborating with CRO representatives.
Advocacy Engagement: Represent the sponsor at local and regional patient advocacy or support group meetings when needed.
Reporting: Track and report site engagement activities, enrollment status, and performance metrics.

Travel Requirements:

This is a very high travel position with at least 75% travel.
Sites will primarily be located in the Central USA region, though travel outside this area may occasionally be required.

Requirements:

Bachelor's degree in a relevant field (life sciences, nursing, healthcare management).
Proven experience in clinical research and site relationship management.
Excellent communication and interpersonal skills.
Proactive problem-solving abilities.
Strong organizational and project management skills.
Solid understanding of GCP and regulatory requirements.
Must reside within 30-45 minutes of one of the following airports: Dallas (DFW), Houston (IAH), Chicago (ORD), Minneapolis (MSP), or Detroit (DTW).

Contract Type:
0.7 FTE

Therapeutic Areas: