CLINICAL RESEARCH COORDINATOR I

Moffitt; Tampa (FL); Hybrid; USD 52,000 - 68,000; Full time

Job summary

Moffitt is seeking a Clinical Research Coordinator I to support patient care, enrollment, and trial coordination in a dynamic cancer research environment. Work involves interacting with patients and study teams to ensure protocol adherence and data integrity across trials at the Moffitt Discovery Center.

The role offers a Monday–Friday schedule with hybrid work after a 90-day training period, relocation assistance may be provided, and opportunities to advance within a leading National Cancer

Qualifications

• Bachelor’s degree preferred in science, health, or business fields.
• CCRP/CCRC or equivalent certification preferred.
• Minimum 1 year of relevant clinical or research experience.

Responsibilities

• Coordinate patient care with medical staff and document per standards.
• Act as liaison between investigators, regulatory staff, and sponsors.
• Screen, enroll and follow study subjects with protocol adherence.
• Manage data, source documentation and adverse event reporting.
• Perform diverse administrative duties with understanding of study procedures.

Skills

Clinical coordination

Regulatory documentation

Patient interaction

Data entry

Education

Bachelor's degree (preferred)

Associate's degree + 2 years experience

Job description

## CLINICAL RESEARCH COORDINATOR IApply: Onsite: Moffitt Discovery Center: Full time: Posted Today: R-143### 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**Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career. This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided. https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/ These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Position Highlights:• Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor.• Act as liaison between the investigators, Moffitt regulatory staff and the sponsor.• Will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.• Responsible for data and source documentation and adverse experience reporting.• Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.• Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.Credentials and Qualifications:• \\*Bachelor’s degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience◦ \\*In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience\\*• CCRP/CCRC or equivalent preferred.