What are the responsibilities and job description for the Clinical Research Assistant position at Perseverance Research Center, LLC?
Job description
Summary Of Responsibilities
The clinical research assistant/coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of Perseverance Research Center (PRC), which are subject to change from time to time.
Roles and Responsibilities
* Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
*Prescreening qualified patients via medical records and telephone calls
* Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately
* Administer sponsor required questionnaires
* Works with PRC members to assist with ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand
* Creates, manages, and maintains source documents for each trial
* Attends teleconferences and Investigator Meetings as requested by research director
* Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections
* Efficiently completes all study tasks delegated to them
* Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required time frame
* Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified time frame indicated in the study contract.
* Oversees data and ensures that it is being entered correctly and resolves any queries issued within required time frame
* Collects and reports Adverse Events
* Collects and reports Serious Adverse Events
* Coordinates monitor site visits and assists with preparation of site visit documentation
* Works with the monitor to make any corrections needed to meet requirements and deadlines as needed
Company Overview
Perseverance Research Center (PRC), is a well established clinical research site located in North Scottsdale. PRC is ran by an experienced group of research professionals who came from a variety of settings including large academic institutions, hospitals, and clinical research organizations, who have dedicated their time focusing on clinical research and education in a variety of therapeutic areas.
At Perseverance Research Center, our mission is to assist pharmaceutical and biotechnology companies through every phase in the clinical trial process. We are committed to improving quality of life for our study participants through new and innovative therapies, as well as providing an unparalleled level of service to our providers. Utilizing our experienced team of clinical research professionals and physicians, PRC is committed to transforming the landscape of how clinical trials are performed.
PRC is dedicated to providing quality patient care and continual attention to clinical excellence and patient safety to assure the best healthcare for all patients. PRC also is committed to further educating medical professionals, combining a team of excellent physicians, researchers and clinical staff to improve quality of life in patients diagnosed with a variety of illnesses.
If you are an assiduous worker who is benevolent and passionate about helping others, we want to hear from you!
We know you will love working with us!