CCRC (Certified Clinical Research Coordinator), CCRP (Certified Clinical Research Professional)
Academic / Research
Forward Clinical Trials, Inc is a growing company searching for a potential candidate for the role of Clinical Research Coordinator.
The Coordinator arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. The position works closely with the Principal Investigator, study sponsors and monitors, and the institutions, to provide support and guidance in various aspects of ongoing clinical studies.
Job Knowledge and Skills
Excellent interpersonal skills to deal effectively with clinicians, patients, auditors, monitors and sponsors.
Knowledge of good clinical practice(GCP), FDA Regulations/Guidelines, HIPAA policies
Excellent organizational skills to independently manage work flow
Familiarity with the CTMS:RealTime preferred.
Ability to prioritize quickly and appropriately
Ability to multi-task
Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Reviews and comprehends each assigned protocol including study proceedings and timelines. inclusion and exclusion criteria, confidentiality and privacy protections.
Working closely with the PI, participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols open to enrollment. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
May attend Investigator meetings requiring travel and report pertinent information back to research team members.
Collaborates with PI and institution to respond to any audit findings and implement-approved recommendation
Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data
Assists in the submission of accurate and timely closeout documents to applicable Federal agencies, and the sponsoring agency in accordance with Federal regulations and institutional policies and procedures.
CCRC or CCRP certification preferred
Two years in a clinical research setting, preferably working as a clinical research coordinator on Industry-Sponsored clinical trials.
Forward Clinical Trials, Inc., led by Seth B. Forman, MD is a rapidly growing Clinical Research Center in Tampa, FL that specializes in Dermatology. Forman Dermatology is a general, surgical and cosmetic practice that generates approximately five thousand (5,000) patient visits a year through our facility.