Clinical Research Coordinator II - GYN

Moffitt Cancer Center is a National Cancer Institute-designated Comprehensive Cancer Center focused on the prevention and cure of cancer. The Clinical Research Coordinator II supports principal investigators in coordinating clinical trials, including patient screening, enrollment, care coordination, documentation, and protocol compliance. The role serves as a liaison among investigators, care providers, regulatory staff, and study sponsors while managing moderately complex studies.

Responsibilities

Supporting the PI in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center

Supporting PI sponsored IND or IDE trials

Coordinating patient care by collaborating with medical staff, and documenting in accordance with standards and regulatory guidelines

Acting as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor

Screening, enrolling, and following study subjects, ensuring protocol compliance and close monitoring while the subjects are on study

Performing all CRC core support and additional responsibilities of more complex studies, with a higher patient volume in comparison to the CRC I

Determining methods and procedures for the coordination of newly assigned studies

Preferred

Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred

CCRP/CCRC or equivalent preferred

Bachelor’s Degree in Science

Business Administration

CCRP/CCRC Certification

Benefits

Monday through Friday schedule

Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period

Paid training and orientation through its CTO (Clinical Trails Office) Academy

Relocation assistance may be provided

Company

Comprehensive cancer hospital and research center

Tampa, Florida, USA

http://moffitt.org/

Founded in 1986

10001+ employees

Qualifications

Two (2) years of clinical trials coordination experience

*Associate's degree considered with two (2) additional years of experience.*

TheCRC II is required to have thorough knowledge of word processing (Microsoft Office Suite), data base entry, and thorough knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research

They should be proficient in the use of EMR systems, clinical trial management systems and various other data capture/reporting systems

This person must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals

A proficient understanding of medical terminology required

The CRC II is required to work under minimal supervision to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing

The ability to prioritize assignments and pace one's-self when working under the pressure of deadlines and work volume is required

Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred

CCRP/CCRC or equivalent preferred

Two (2) years of clinical trials coordination experience.

Required skills

Clinical trials coordination, Clinical Practice (GCP), Human-subjects research regulations, Microsoft Office Suite, Electronic medical records (EMR) systems, Clinical trial management systems, Data capture and reporting systems, Medical terminology, CCRP/CCRC certification, Relationship management

Preferred skills

CCRP/CCRC or equivalent preferred

Experience

2+ years