We are seeking an experienced full time Clinical Research Coordinator, preferably an RN, responsible for coordinating and conducting ALL aspects of clinical drug studies, from pre-study planning and recruitment through successful completion of all patient visits, and understanding of regulatory documentation. We have many new studies in various modalities.
We are committed to excellence and looking for the best!
Competitive salary and high earning potential
Highly involved P.I. on site with over 30 years of research experience
Recruitment and regulatory support team
Conduct Clinical Research studies in Multi-Therapeutic areas
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements
Responsible for the completion of all study documentation forms, including case report forms and other study specific documents
Patient recruitment and pre-screening of patients
Interacting with the Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed, alerting the Principal Investigator of serious adverse events
Interacting with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process
Confirming clinical research in compliance with all applicable regulations
Conducting EKGs and Spirometry
Giving injections and IVs
Work flexible hours
Occasional travel for attendance at investigator meetings
Education and Experience:
ACRP certification preferred
Certification in Basic Cardiac Life Support (BCLS) is required
1 + year of Medical experience
3 + years of Clinical Research experience
Current State Nursing License (RN or LPN) or Certificate of Completion of accredited MA Program
Skills and Abilities:
Must hold strong clinical skills Strong knowledge of GCP guidelines and Federal Regulations
Excellent communication skills
Professional and dependable
Strong multitasking abilities
Ability to treat and assist ill, older, or distraught patients
Computer literate and familiar with Microsoft Word, Excel, and EMRs
Background in medical history intake and medical terminology
Ability to work well with co-workers, peers, monitors and potential subjects
Ability to effectively and efficiently handle multiple tasks simultaneously with precision and adhere to sponsor requirements
Strict attention to detail and strong organization skills.
The candidate should be able to promote a teamwork philosophy with a positive attitude
Must be a quick learner and able to initiate and complete work without supervision.
Additional Salary Information: We offer a highly competitive salary structure with the potential for regularly earning additional income
St. Francis Medical Institute is dedicated to the physical, psychological, and spiritual well-being of our patients. We successfully address a wide range of healthcare issues by offering our patients individualized attention in our beautiful and welcoming environment from one of the top physicians in the U.S. Frank Averill, and his professional staff provide comprehensive diagnosis, treatment, and... strategies to help prevent future health concerns. Our Clinical Research Center provides a critical service to bio-pharmaceutical companies by conducting clinical research in various therapeutic areas. Current areas of study include: asthma, COPD, dermatology and sleep.