Clinical Trial Liaison

137447
  • 145000 USD - 160000 USD
  • Dallas, United States
  • Permanent

All candidates must be based in Texas or Georgia and have a strong oncology clinical operations background. The targeted start date for this role is February.

 

Our client is seeking a motivated and detail-oriented individual to join our team as a Clinical Trial Liaison. The Clinical Trial Liaison will play a crucial role in our clinical operations by serving as the primary point of contact between our client and clinical trial sites. This individual will work closely with clinicians, nurses, and other healthcare professionals at the clinical sites to ensure the smooth and efficient conduct of our clinical trials.

 

Responsibilities:

  • Collaborate with clinical trial sites: Establish and maintain strong relationships with clinicians, nurses, and other healthcare professionals at the clinical trial sites. Serve as the main point of contact for any questions or concerns related to the clinical trials.
  • Real-time data collection: Work closely with clinical trial sites to gather real-time data on patient recruitment, enrollment, treatment, and outcomes. Ensure that data is collected accurately and in accordance with the study protocols and regulatory requirements.
  • Communication with Client team: Act as a liaison between the clinical trial sites and the Client pharma team. Provide regular updates on the progress of the clinical trials, including any issues or challenges that may arise.
  • Outgoing operations: Coordinate outgoing operations related to the clinical trials, including the shipment of print material and other necessary items between Client and the clinical trial sites.
  • Compliance and documentation: Ensure compliance with all regulatory requirements and internal policies related to the conduct of clinical trials. Maintain accurate and up-to-date documentation of all communication and activities related to the clinical trials.
  • Disseminates information for the clinician audience about clinical issues during emergencies, including updated clinical guidelines.
  • Collects and compiles clinical inquires to inform communication strategies.

Qualifications:

• Bachelor's Degree (Masters of Public Health, RN, BSN or similar, preferred) and 5+ years of related communications experience in clinical or nursing environments.

• Previous experience in clinical research or healthcare industry preferred.

• Strong communication and interpersonal skills.

• Ability to work independently and as part of a team.

• Excellent organizational and time management skills.

• Knowledge of regulatory requirements governing clinical trials (e.g., FDA regulations, ICH-GCP guidelines) is a plus.
 

This is an exciting opportunity to join a dynamic and growing company at the forefront of precision oncology. If you are passionate about making a difference in the lives of cancer patients and are looking for a challenging and rewarding career, we encourage you to apply.

Amanda Blunck Lead Recruiter

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