Clinical Research Coordinator - Contract - Longmont, CO
Lead the heartbeat of clinical trials-where precision meets patient care.
Proclinical is seeking a Clinical Research Coordinator for a contract role in Longmont, CO.
Primary Responsibilities:
The successful candidate will oversee the daily operations and management of assigned clinical trials, ensuring compliance with protocols, regulatory requirements, and company procedures. You will collaborate with various stakeholders, including study sponsors, monitors, investigators, and site management, to ensure the success of clinical trials. This role also involves mentoring junior team members and addressing challenges that may arise during the studies.
Skills & Requirements:
- Experience in clinical research, with a strong understanding of trial protocols and regulatory compliance.
- Proficiency in phlebotomy and handling laboratory specimens.
- Strong organizational skills and attention to detail for data collection and documentation.
- Ability to communicate effectively with diverse stakeholders, including patients, investigators, and sponsors.
- Problem-solving skills to address protocol deviations or unexpected challenges.
- Familiarity with electronic data capture (EDC) systems and good documentation practices.
The Clinical Research Coordinator's responsibilities will be:
- Manage the enrollment process for clinical trials, aiming to exceed recruitment goals.
- Collaborate with recruitment teams and site management to optimize patient recruitment strategies.
- Educate patients or caregivers about study details and associated procedures.
- Monitor study activities to ensure adherence to protocols and regulatory standards.
- Maintain and regularly update study e-regulatory binders, ensuring compliance.
- Guide and support junior coordinators in following protocols and regulatory guidelines.
- Schedule study visits and monitor timelines according to protocol requirements.
- Collect and document data accurately during patient visits, adhering to good documentation practices.
- Enter collected data into electronic data capture (EDC) systems promptly and resolve queries within set timelines.
- Manage inventory of lab and study supplies to meet study needs and enrollment goals.
- Attend investigator meetings and site initiation visits, gathering relevant study information.
- Perform protocol-specific procedures such as vital signs, electrocardiograms, and specimen collection.
- Record and report adverse events, ensuring proper documentation and communication with investigators.
- Oversee drug accountability, including logging shipments, dispensing medication, and maintaining accurate records.
- Maintain master logs, training logs, and delegation logs for assigned studies.
- Participate in quality assurance audits and ensure investigational product (IP) management meets protocol requirements.
- Safeguard patient health information and sponsor confidentiality.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@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.
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