Clinical Research Coordinator I - Heme/Myeloid

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 52,000 - 65,000; Full time

Benefits offered by this job

Hybrid work after training period

Relocation assistance

Paid training and orientation

CTO Academy

Job summary

Moffitt Cancer Center in Tampa, FL is seeking a Clinical Research Coordinator I to support Heme/Myeloid trials. This role involves direct patient interaction, screening and enrolling participants, educating them about trial participation, and guiding them through study procedures within a therapeutic clinical trial framework.

You will work with physicians, pharmacists, nurses, and data managers to ensure protocol compliance, data integrity, and safety reporting, while benefiting from a hybrid

Qualifications

• Coordinate patient care and ensure protocol adherence under supervisor.
• Screen, enroll, and follow study subjects with regulatory compliance.
• Maintain data integrity and adverse event reporting.
• Prepare documentation and communicate with sponsors and team.

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with guidelines.
• Screen, enroll, and monitor subjects while ensuring protocol compliance.
• Manage data and source documentation and adverse event reporting.
• Support trial logistics and administrative procedures under supervision.

Skills

Clinical coordination

Regulatory knowledge

Documentation

Customer service

Education

Bachelor’s degree (preferred in scientific/ health related/ business)

Associate’s degree with 2 years relevant experience

Tools

CCRP/CCRC certification preferred

Job description

Clinical Research Coordinator I - Heme/Myeloid - Moffitt Cancer Center### Clinical Research Coordinator I - Heme/MyeloidApply: Hybrid (Part -time in Office): Moffitt Discovery Center: Full time: Posted Today: R-5354### 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. 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. ## Clinical Research Coordinator I **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.**Salary Range***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.* *We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.*