Clinical Research Coordinator I - Head & Neck

Moffitt Cancer Center

United States

Hybrid

USD 50,000 - 75,000

Full time

4 days ago
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Benefits offered by this job

Paid training
CTO Academy
Relocation assistance

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator to join a dynamic team advancing cancer treatment through clinical trials. You will work directly with patients, coordinate enrollment, educate participants, and help ensure trials progress safely and smoothly in alignment with approved protocols.

The role supports hybrid work after a 90-day onboarding period, with paid training through the CTO Academy and relocation assistance if needed. Relocation may be provided.

Qualifications

  • Bachelor’s degree with 1 year of relevant clinical, health-related, scientific, business or research experience.
  • Alternatively, an associate’s degree with 2 years of relevant experience may qualify.
  • CCRP/CCRC or equivalent credential is preferred.

Responsibilities

  • Coordinate patient care with medical staff and document per standards and regulatory guidelines.
  • Serve as liaison between investigators, regulatory staff, and sponsor.
  • Screen, enroll and follow subjects, ensuring protocol compliance and safety.
  • Manage data and source documentation, including adverse event reporting.
  • Perform diverse administrative duties with judgment and knowledge of study protocol.

Skills

Clinical trial coordination
Subject enrollment
Regulatory documentation
Data management
Team collaboration

Education

Bachelor’s degree in scientific/health/business admin
Associate’s degree with 2 years relevant experience
CCRP/CCRC or equivalent

Job description

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/

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.

Moffitt Career Site

Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

Reasonable Accommodation

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at HRReceptionists@moffitt.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. Read more information about yourEEO rights under the law.

Transparency in Coverage Rule Careers

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.

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