Excel Medical Clinical Trials, LLC is seeking a qualified Clinical Research Coordinator (CRC) for a busy and rapidly growing clinical research site for Phase 1-IV studies. General responsibilities include performing a variety of clinical and administrative tasks required for successful operation of a clinical study.
Candidate must possess the following:
Impeccable organizational skills and attention to detail.
Commitment to excellence and quality patient care.
Excellent communication, writing, and interpersonal skills.
Ethical compass that compels the candidate to be honest, detail-oriented, and self-driven.
High level critical thinking skills.
Knowledge of medical terminology and lab collection/processing/storage procedures.
Proficiency with computers and Microsoft Office Suite.
Understand in detail all applicable study protocols to ensure completion of clinical trial activities.
Execute study protocol procedures in detailed, organized, and professional manner.
Perform lab draws, and when necessary, process and prepare specimens for shipment.
Must uphold federally-mandated guidelines and monitor and protect the safety and welfare of all study patients, as well as practices of informed consent and Good Clinical Practice.
Effectively, accurately, and promptly document, notify and report any adverse events and Serious Adverse Events to Sponsor.
Complete study source documentation.
Enter study data into computerized databases.
Serve as a liaison between Site, assigned Clinical Research Associate (CRA), and Sponsor/CRO.
Coordinate timing and schedule study visits throughout the duration of the trial.
Maintain study files and study-specific supplies.
Effectively communicate with study research team, Principal/Sub-investigators, Sponsors/CROs, and study patients.
Actively participate in site visits from Sponsors/CROs, including site qualification, monitoring, and closeout visits.
May be required to travel in the US to attend Investigator Meetings (<5% per year).
Previous CRC experience (minimum 5 years).
Phlebotomy certification and experience.
Bilingual (English/Spanish) is a plus.
Clear understanding of ICH, FDA, and GCP regulatory requirements.
Internal Number: 001
About Excel Medical Clinical Trials, LLC
Excel Medical Clinical Trials conducts preeminent pharmaceutical and genetic clinical trials in Boca Raton, Florida. We offer patients the highest level of integrity, professionalism, and safety. We offer sponsors a genuinely experienced research site, comprising a consortium of carefully-vetted clinicians from diverse specialties and an exemplary staff. Our team is eminently-qualified, impeccably-trained, and uncompromisingly-compassionate; they are compulsive, and diligent. Excel Medical Clinical Trials brings Boca Raton a research site of which it can be exceptionally proud.