Clinical Research Coordinator III Job at Proclinical Staffing, Austin, TX

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  • Proclinical Staffing
  • Austin, TX

Job Description

Clinical Research Coordinator III - Permanent - Austin, Texas

Join the Brainiacs: Unleash your inner scientist at our client's Research Institute!

Proclinical is seeking a Clinical Research Coordinator III to manage and oversee a variety of clinical studies. This role involves administrative duties, regulatory functions, and mentoring junior coordinators.

Primary Responsibilities:

The successful candidate will be the primary point of contact for study sponsors, monitors, and site managers, ensuring all trials are conducted efficiently from start to finish. Your expertise will be crucial in problem-solving and planning clinical trials, with minimal oversight required.

Skills & Requirements:

  • Proven experience leading multiple clinical trials as a lead coordinator.
  • Strong independent and team-working abilities.
  • Effective training and communication skills.
  • Proficiency in English and medical terminology.
  • Willingness to travel for training and support at various sites.

The Clinical Research Coordinator III's responsibilities will be:

  • Achieve and exceed enrollment goals for clinical trials.
  • Collaborate with recruitment and site management to optimize recruitment strategies.
  • Educate participants or caregivers about study procedures.
  • Train and monitor study team compliance with protocols and regulations.
  • Ensure accurate and timely data collection and entry.
  • Maintain and audit study e-regulatory binders for compliance.
  • Schedule and prepare for study visits according to protocol.
  • Manage inventory of lab and study supplies.
  • Attend investigator meetings and site initiation visits.
  • Maintain records of study activities and manage drug accountability.
  • Communicate and resolve laboratory findings and adverse events.
  • Oversee specimen management and drug dispensation.
  • Identify and address protocol deviations or unanticipated events.
  • Prepare for quality assurance audits and maintain safety reports.
  • Provide expert guidance and support to peers.
  • Maintain confidentiality of patient and sponsor information.

If you are having difficulty in applying or if you have any questions, please contact Nico Kohlwes at n.kohlwes@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

Job Tags

Permanent employment,

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