Clinical Research Coordinator - Contract - Edmond, OK
Make your mark in global health by managing high-impact clinical research within a leading contract research organisation!
Proclinical is seeking a Clinical Research Coordinator II to oversee the daily operations and management of assigned clinical trials.
Primary Responsibilities:
This role involves administrative duties, regulatory compliance, and collaboration with various stakeholders, including study sponsors, monitors, CROs, and site management. You will also provide guidance and training to junior team members while ensuring adherence to standard operating procedures (SOPs) and protocols.
Skills & Requirements:
- Experience in clinical research, including knowledge of regulatory compliance and study protocols.
- Proficiency in phlebotomy.
- Strong organizational and communication skills.
- Ability to manage multiple tasks and prioritize effectively.
- Attention to detail and commitment to maintaining high-quality documentation.
- 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, identifying strategies to exceed recruitment goals.
- Collaborate with recruitment teams and site management to optimize recruitment practices.
- Educate patients or caregivers about study details and procedures.
- Monitor study activities to ensure compliance with protocols and regulatory requirements.
- Maintain and update study e-regulatory binders, ensuring all documentation is accurate and complete.
- Schedule study visits and monitor schedules in alignment with protocols and study plans.
- Complete source documentation during patient visits, ensuring accuracy and adherence to good documentation practices.
- Enter collected data into electronic data capture (EDC) systems within one business day and resolve data queries promptly.
- Manage inventory of lab and study supplies to meet study requirements and enrollment goals.
- Attend investigator meetings and site initiation visits, gathering relevant study information.
- Maintain records of study activities, including case report forms and drug dispensation logs.
- Perform protocol-specific procedures such as vital signs, electrocardiograms, and specimen collection.
- Communicate with laboratories and investigators regarding findings and adverse events.
- Oversee drug accountability, including logging shipments, dispensing medication, and maintaining accurate records.
- Identify and address protocol deviations or unanticipated events.
- Participate in quality assurance audits and ensure investigational product (IP) management, including proper storage and restricted access.
- Maintain training and delegation logs, as well as safety reports, ensuring compliance with review and signature requirements.
- Uphold confidentiality of patient health information and sponsor data.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerhcio@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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