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Clinical Research Coordinator
Clinical Research CoordinatorProclinical • Fort Collins, USA
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Clinical Research Coordinator

Clinical Research Coordinator

Proclinical • Fort Collins, USA
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Clinical Research Coordinator - Contract - Fort Collins, CO

Are you looking to drive groundbreaking medical research and make a real impact? Join our client and lead the way in advancing clinical trials!

Proclinical is seeking a Clinical Research Coordinator II to oversee the daily operations and management of assigned clinical trials.

Primary Responsibilities :

In this role, you will ensure compliance with protocols, regulatory requirements, and organizational standards while collaborating with internal and external stakeholders. You will also provide guidance and training to junior team members and contribute to the success of clinical trial enrollment and execution.

Skills & Requirements :

  • Experience in clinical research operations.
  • Proficiency in phlebotomy.
  • Strong organizational and communication skills.
  • Ability to interpret complex medical data and perform protocol-specific procedures.
  • Familiarity with electronic data capture systems and regulatory compliance.
  • Attention to detail and problem-solving capabilities.

The Clinical Research Coordinator's responsibilities will be :

  • Manage daily operations of assigned clinical trials, including administrative and regulatory tasks.
  • Collaborate with recruitment teams and site management to optimize patient enrollment strategies.
  • Inform patients or caregivers about study procedures and protocols.
  • Monitor study activities to ensure compliance with local, federal, and state regulations.
  • Maintain and update study e-regulatory binders, ensuring all documentation is accurate and complete.
  • Schedule study visits and monitor timelines according to protocol requirements.
  • Collect and document data during patient visits, ensuring accuracy and adherence to good documentation practices.
  • Enter collected data into electronic data capture (EDC) systems within required timelines and resolve queries promptly.
  • Manage inventory of lab and study supplies to meet enrollment and study visit needs.
  • Attend investigator meetings and site initiation visits, gathering relevant study information.
  • Perform protocol-specific procedures such as vital signs, electrocardiograms, and specimen collection.
  • Record adverse events and collaborate with investigators for proper reporting.
  • Dispense medical devices or drugs, calculate dosages, and provide instructions as needed.
  • Identify and address protocol deviations or unanticipated events.
  • Maintain investigational product accountability, including logging shipments and dispensed medication.
  • Ensure proper storage and restricted access for investigational products.
  • Participate in quality assurance audits and maintain accurate study logs.
  • Ensure confidentiality of patient health information and sponsor data.

    • Compensation :

  • $25 to $28 per hour.
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    Clinical Research Coordinator • Fort Collins, USA

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