Clinical Research Coordinator II

SPEROS; Tampa, Northern (FL, KY); Hybrid; USD 40,000 - 61,000; Full time

Job summary

The Clinical Research Coordinator II at Moffitt Cancer Center in Tampa, FL, supports the PI in clinical trials by coordinating research activities, ensuring regulatory compliance, and managing data capture.

This development role requires an Associate's degree (Bachelor's preferred), proficiency with EMR and trial management systems, and strong communication skills to liaise with investigators, staff, and sponsors.

Qualifications

• Requires associate degree; bachelor’s preferred in scientific/health field.
• Proficient in Microsoft Office, data entry, and Good Clinical Practices compliance.
• Strong communication and interpersonal skills with patients and staff.

Responsibilities

• Coordinate protocols and trial activities under supervision.
• Screen, enroll, and monitor study subjects per protocol.
• Communicate with investigators, care providers, and sponsors.
• Maintain regulatory documentation and data accuracy.

Skills

Verbal and written communication

Interpersonal skills

Prioritization and time management

Attention to detail

Education

Associate's degree in health/science or related field

Bachelor's degree preferred

Tools

Microsoft Office Suite

Clinical trial management systems

EMR systems

Data capture/reporting systems

Job description

## Clinical Research Coordinator IIApply: Hybrid (Part -time in Office): Clinical Support Building: Full time: Posted Today: R-3888### Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.### As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.**Summary**The Clinical Research Coordinator II (CRC II) is a second level in the CRC career path within Clinical Trials. It is a development career position supporting the PI in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center. The CRC II may also support PI sponsored IND or IDE trials. As the primary resource for the protocols, the CRC II will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines. The CRC II will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, the CRC II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. The CRC II will perform all CRC core support and additional responsibilities of more complex studies, with a higher patient volume in comparison to the CRC I. The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies. The supervisor or Principal Investigator will provide more detailed instructions on new complex assignments where there is limited prior depth, or breadth of knowledge or working experience.Moderate supervision provided while developing latitude for independent judgment. Still developing and acquiring higher level knowledge and skills, while working on moderate scope complexity where analysis of situations or data requires a review of a variety of factors. Solves a range of straight forward problems using prescribed guidelines and policies. Limited problem solving while working under defined guidelines. Continues to build productive internal/external working relationships.**Job Title:** Clinical Research Coordinator II **Minimum Education Level:** Associate's Degree **Minimum Field of Study:** preferred scientific, health related or business administration program **Minimum Education Notes:** **Preferred Education Level:** Bachelor's Degree **Preferred Field of Study:** **Preferred Education Notes:** **Licensure Certification Needed:** No **Minimum Licensure:** **Minimum Licensure (Other):** **Training Required:** CRC II is required to have through knowledge of word processing (Microsoft Office Suite), data base entry, and through knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research. Should be proficient in the use of EMR systems, clinical trial management systems and other various data capture/reporting systems. Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals. Proficient understanding of medical terminology required. 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. Must have ability to prioritize and pace one’s-self when working under the pressure of deadlines and work volume. Successfully demonstrates competency by meeting established competency guideline/check list annually. **Preferred Licensure (Other):** CCRP/CCRC or equivalent**Salary Range**$29.05 - $44.28*Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.*