Proclinical Staffing
Base pay range
$20.00/hr - $25.00/hr
Consultant/Client Lead at Proclinical Staffing Clinical Research Coordinator - Contract - Denver CO
Position Overview Proclinical is seeking a Clinical Research Coordinator II to oversee the daily operations and management of assigned clinical trials.
Primary Responsibilities
Manage and oversee clinical trial enrollment, identifying strategies to exceed recruitment goals.
Collaborate with recruitment teams and site management to optimize recruitment practices.
Educate patients or caregivers about study procedures and requirements.
Monitor study activities to ensure compliance with protocols and regulatory guidelines.
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 timely entry into electronic data capture (EDC) systems.
Address and resolve data queries within specified timeframes.
Manage inventory of lab and study supplies to meet study 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 and report adverse events, collaborating with investigators as needed.
Ensure proper 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 maintain accurate master logs for each study.
Oversee investigational product (IP) management, ensuring proper storage, labeling, 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.
Skills & Requirements
Experience in clinical research, with a strong understanding of regulatory compliance and protocols.
Proficiency in data collection, documentation, and electronic data capture systems.
Strong organizational skills to manage study supplies, schedules, and documentation.
Ability to perform medical procedures such as vital signs, ECGs, and specimen collection.
Effective communication skills for interacting with patients, investigators, and study sponsors.
Problem‑solving skills to address protocol deviations and operational challenges.
Commitment to maintaining confidentiality and ethical standards.
Contact:
Jackie Cerchio
at
j.cerchio@proclinical.com
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 - https://www.proclinical.com/privacy-policy
#J-18808-Ljbffr
Consultant/Client Lead at Proclinical Staffing Clinical Research Coordinator - Contract - Denver CO
Position Overview Proclinical is seeking a Clinical Research Coordinator II to oversee the daily operations and management of assigned clinical trials.
Primary Responsibilities
Manage and oversee clinical trial enrollment, identifying strategies to exceed recruitment goals.
Collaborate with recruitment teams and site management to optimize recruitment practices.
Educate patients or caregivers about study procedures and requirements.
Monitor study activities to ensure compliance with protocols and regulatory guidelines.
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 timely entry into electronic data capture (EDC) systems.
Address and resolve data queries within specified timeframes.
Manage inventory of lab and study supplies to meet study 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 and report adverse events, collaborating with investigators as needed.
Ensure proper 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 maintain accurate master logs for each study.
Oversee investigational product (IP) management, ensuring proper storage, labeling, 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.
Skills & Requirements
Experience in clinical research, with a strong understanding of regulatory compliance and protocols.
Proficiency in data collection, documentation, and electronic data capture systems.
Strong organizational skills to manage study supplies, schedules, and documentation.
Ability to perform medical procedures such as vital signs, ECGs, and specimen collection.
Effective communication skills for interacting with patients, investigators, and study sponsors.
Problem‑solving skills to address protocol deviations and operational challenges.
Commitment to maintaining confidentiality and ethical standards.
Contact:
Jackie Cerchio
at
j.cerchio@proclinical.com
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 - https://www.proclinical.com/privacy-policy
#J-18808-Ljbffr