Clinical Research Coordinator - Various Levels

Moffitt; Tampa (FL); Hybrid; USD 36,000 - 55,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Moffitt Cancer Center seeks a Clinical Research Coordinator at various levels to support innovative cancer trials across multiple sites in Florida. You will partner with physicians, nurses, pharmacists, and sponsors to translate protocols into patient-centered trial activities.

The role emphasizes screening, enrollment, patient education, documentation, and cross-team coordination, with hybrid on-site and remote work after training.

Qualifications

• Bachelor's degree required; two years of clinical trials experience or related coordination.
• Associate degree required; two years of relevant experience with HS or GED accepted in lieu of degree.

Responsibilities

• Screening, recruiting and enrolling research participants.
• Educating patients and families about trials.
• Coordinating research patient care and protocol procedures.
• Facilitating visits and procedures for participants.
• Supporting safety and protocol compliance.
• Maintaining accurate research documentation.
• Coordinating across multiple clinical and research teams and sponsors.

Skills

Clinical trials coordination

Data entry

Regulatory knowledge

Written and verbal communication

Education

Bachelor's degree

Associate degree

Job description

Clinical Research Coordinator - Various Levels - Moffitt Cancer Center### Clinical Research Coordinator - Various LevelsApply: Hybrid (Part -time in Office): Magnolia Hospital: Moffitt Speros Outpatient Center and the Richard M. Schulze Family Foundation Proton Center: Moffitt South Shore: Moffitt Cancer Center at International Plaza: Full time: Posted Yesterday: End Date: November 18, 2026 (5 days left to apply): R-5891### 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**Clinical Research Coordinator Opportunities Help Bring Tomorrow’s Cancer Treatments to Patients Today What if your work could help bring the next cancer treatment to a patient who needs it? At Moffitt Cancer Center, Clinical Research Coordinators are at the heart of making that possible. As a Clinical Research Coordinator, you will help bring innovative clinical trials to life while supporting patients and families through one of the most important parts of their cancer journey. This is more than coordinating a study. You will become a trusted connection between the patient, investigator, clinical care team, and clinical trial sponsor, helping translate a complex research protocol into a safe, coordinated experience for each patient. From screening and enrollment through treatment and follow-up, you will help patients understand what to expect, coordinate research visits and protocol-required activities, maintain accurate research documentation, and ensure important study requirements are completed. You will collaborate across Moffitt with physicians, nurses, pharmacists, research teams, regulatory professionals, data teams, and other clinical departments, while also working with study sponsors ranging from emerging biotechnology companies to leading pharmaceutical organizations. Moffitt's current CRC role expectations include screening, recruiting and enrolling research participants; educating patients and families; coordinating research patient care; facilitating visits and procedures; supporting safety and protocol compliance; maintaining research documentation; and coordinating across multiple clinical and research team Why Clinical Research at Moffitt? Make a difference for patients. You will work directly with patients and families, helping them navigate the clinical trial experience and serving as a consistent resource for trial-related questions and coordination. Moffitt's patient guidance identifies the CRC as the patient's primary point of contact for trial-related questions and support. Be part of advancing cancer treatment. You will work alongside teams delivering clinical trials of new cancer treatments and help turn complex research protocols into carefully coordinated patient experiences. Moffitt's Clinical Trials Office supports investigators conducting clinical trials of new treatments and provides services spanning protocol activation, enrollment, study-related patient care, data collection, compliance, and training. Build relationships across an incredible team. Clinical research is highly collaborative. CRCs serve as an important connection among patients, investigators, care providers, regulatory teams, sponsors and other partners involved in delivering a clinical trial. Use your critical thinking and problem-solving skills. Every patient and every clinical trial is different. Successful CRCs must be able to organize complex activities, communicate effectively, adapt to changing patient and protocol needs, identify concerns, and know when to escalate issues for clinical or investigator input. Grow your career in clinical research. Moffitt's CRC career structure provides progressive levels of responsibility. As coordinators gain experience, they can take on increasingly complex trials and patient populations, work with greater independence, mentor other coordinators, contribute to process improvement, and serve as subject matter experts**You May Be a Great Fit If You...**We welcome candidates from a variety of professional and educational backgrounds, including healthcare, biological sciences, public health, social work, psychology, sociology, communications, business, humanities, and other related fields.You may thrive as a Clinical Research Coordinator if you:* Enjoy working directly with patients and families.* Are an organized problem-solver who can manage multiple priorities.* Communicate clearly and build strong relationships.* Enjoy working as part of a multidisciplinary team.* Bring curiosity, initiative, good judgment, and a willingness to learn.* Can adapt quickly when patient needs or priorities change.* Are comfortable working in a detailed, highly coordinated environment.* Are excited to learn clinical research regulations, study protocols, and Good Clinical Practice requirements.* Have previous clinical research experience, or relevant experience that can translate to clinical research.At Moffitt, effective CRC practice requires collaboration, critical thinking, flexibility, organization, patient coordination, protocol compliance, and attention to patient safety and data integrity.**Training, Schedule & Career Path**Moffitt provides training and orientation through the **Human Subject Research (HSR) Academy** for introduction to good clinical practice and clinical research workflows and **Clinical Trials Office (CTO)** for science and disease specific training, helping team members build the knowledge and skills needed to succeed in clinical research.* **Monday through Friday schedule*** **Hybrid work opportunity** combining on-site and remote work following successful completion of the 90-day introductory and training period* **Multiple CRC career levels** based on education and experience* **Relocation assistance may be available****Find the Opportunity That Matches Your Experience****Clinical Trials Screening Coordinator*** Bachelor's degree required.* Two years of experience in clinical trials, such as patient-facing coordination, data management, regulatory, or other research coordination.* Knowledge of clinical research processes, procedures, and protocols.**Associate Clinical Research Coordinator*** Associate degree required.* In lieu of an associate degree, two years of relevant experience with a high school diploma or GED.* Experience with data entry and strong written, verbal, and organizational skills.**Clinical Research Coordinator I*** Bachelor's degree with one year of relevant clinical, health-related, scientific, business, or research experience.* In lieu of a bachelor's degree, an associate degree with an additional year of relevant experience, for a total of two years of experience.**Clinical Research Coordinator II*** Bachelor's degree with two years of clinical trials coordination experience.* In lieu of a bachelor's degree, an associate degree with four years of clinical trials coordination experience may be considered.* CCRP, CCRC, or equivalent certification preferred.**Clinical Research Coordinator III*** Bachelor's degree with four years of clinical trials coordination experience.* In lieu of a bachelor's degree, an associate degree with six years of clinical trials coordination experience may be considered.* CCRP or CCRC certification required.**Senior Clinical Research Coordinator*** Bachelor's degree with six years of clinical trial coordination experience.* In lieu of a bachelor's degree, an associate degree with an additional two years of clinical trials coordination experience, for a total of eight years, may be considered.* CCRP or CCRC certification required.**Bring Your Skills. Build Your Career. Make an Impact.**If you are looking for work that combines **patients, science, teamwork, problem-solving, and purpose**, a career in clinical research at Moffitt may be the opportunity you have been looking for.**Come help us bring tomorrow's cancer treatments to patients today.****Salary Range**$26.32 - $40.14*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.*