This is an opportunity for an experienced Senior Clinical Research Coordinator to contribute to medical research as part of one of the largest HIV related trials in history. The ideal candidate understands the importance of the clinical research process and has experience in all the responsibilities of a research coordination (consenting, phlebotomy, labs, EDC, and sponsor monitoring visits).
For the right motivated candidate, this is an excellent opportunity to work with passionate and engaged Principal Investigators, while also contributing to the growth of the company.
Primary coordinator on two large HIV related studies
Work with Principal Investigators to see patients and manage their clinical care throughout the trial
Discuss study protocols with patients and verify the informed consent documentation
Meet with a patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study
Dispense study medication in a professional and accountable manner following protocol requirements
Collect, process, and ship blood/urine specimens at scheduled patient visits
Perform ECGs and obtain vital signs of patients
Schedule all patient research visits and procedures consistent with protocol requirements
Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy
Maintain accurate and complete regulatory files
Prepare for monitor visits
Administer questionnaires/diaries per protocol
Requirements and Qualifications:
Minimum four years of experience on-site as a research coordinator in pharma or device clinical trials.
Venipuncture / EKG experience
Excellent written and verbal communication skills
About Research & Development Institute
Research & Development Institute (RDI) is a leading in the clinical research industry, with over 110 clinical trials completed since its establishment in 2008. The company boasts a national network of physicians & labs and supplies the largest BioTech companies with the research data they need to improve healthcare worldwide.
The Company has the ability to sponsor clinical trials as a Contract Research Organization as well as provide qualified physician sites through its Site Management Network,