Job Description

Summary Description
We are looking for Experienced Clinical Research Coordinators to work on Phase II and III clinical trials. Our sites are located in Jupiter and Port St. Lucie, Florida and conduct Vaccine work as well as many therapeutic areas of General Medicine. Clinical Research Coordinators are responsible for following research protocols for accurate completion of study visits, adhering to regulatory standards and participating in ongoing study specific training, among other duties. Other duties typically include Phlebotomy, taking Vitals, and ECG's as well as processing and shipping Labs.
Responsibilities
Overseeing the smooth running of clinical trials.
Collecting data obtained from research.
Informing participants about study objectives.
Administering questionnaires.
Monitoring research participants to ensure adherence to study rules.
Adhering to research regulatory standards.
Adhering to ethical standards.
Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
Liaising with laboratories regarding results.
Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
Engaging with subjects and understanding their concerns.
Qualifications
Associates degree in Nursing or related field. MA's, CNA's, LPN's, RN's considered as well as those with specific CRC experience without these degrees.
2+ years in healthcare.
Analytical mindset.
Attention to detail.
Exceptional interpersonal skills.
Outstanding written and verbal communication.
Excellent organizational skill.
Willingness to continually self-educate.

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