Associate Clinical Research Coordinator-Breast
About the role
Moffitt Cancer Center is a National Cancer Institute-designated Comprehensive Cancer Center located in Florida. It employs a dedicated team of nearly 11,000 members who are working towards preventing and curing cancer. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is consistently named one of the Tampa Bay Times’ Top Workplaces.
Responsibilities
- Interact directly with patients, patient families, study sponsors, and the Clinical Trial Team.
- Coordinate activities related to assigned research protocols, including obtaining informed consent from study participants, specimen collection, and data entry.
- Support therapeutic studies by completing data entry into various database systems, following protocol, and maintaining regulatory documents.
- Facilitate the collection of study-required specimens and communicate with study sponsors.
- Apply job skills and company policies to complete assigned tasks within semi-routine assignments.
Requirements
- Achieve effective communication, good decision-making, and a sense of urgency and enthusiasm.
- Show excellent teamwork skills and the ability to collaborate with diverse backgrounds and experiences.
- Have prior experience in clinical trials or the ability to successfully learn this.
- Experience interacting with patients and coordinating care with medical staff.
- Gain a solid understanding of regulatory guidelines and following a clinical trial protocol.
Qualifications
- A minimum of an Associate’s degree, or 2 years of relevant experience in lieu of a degree, with a high school diploma or GED.
- A Bachelor’s degree preferred in scientific, health-related, or business administration programs.
Skills
- Effective communication skills.
- Good decision-making abilities.
- Eagerness to embrace challenges with a sense of urgency and enthusiasm.
- Time management skills.
- Excellent teamwork skills.
- Ability to collaborate with those from diverse backgrounds and experiences.
- Prior experience in clinical trials.
- Familiarity with regulatory requirements in clinical research or ability to successfully learn this.
- Experience interacting with patients and coordinating care with medical staff.
- Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol.
Benefits
Moffitt Cancer Center offers a Monday through Friday schedule and a hybrid work (mix of remote and on-site) after a 90-day introductory and training period. Relocation assistance may be provided.
Pay
The salary range for this position is $21.65 - $33.05. 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.
Schedule
This position offers a Monday through Friday schedule and a hybrid work (mix of remote and on-site) after a 90-day introductory and training period.
Benefits
Moffitt Cancer Center offers benefits such as paid training and orientation through its CTO (Clinical Trials Office) Academy. Relocation assistance may be provided.