CLINICAL TRIALS SCREENING COORDINATOR I

About the role

The Clinical Trials Screening Coordinator I reports to the Clinical Trials Office but will directly support a specific Disease Site Program. This position is embedded in the clinic to serve as a single point of contact to aid physicians, clinical team members and research personnel with timely identification of patients for consideration for clinical trial enrollment. The role performs an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program. The role has the primary responsibility for referring physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials.

Responsibilities

• Serve as a single point of contact to aid physicians, clinical team members and research personnel with timely identification of patients for consideration for clinical trial enrollment.
• Perform an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program.
• Have the primary responsibility for referring physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials.
• Support the PI in clinical trials within the clinical trials career path.

Requirements

• Bachelor's degree in science, health-related field or related project management.
• 2 years' experience in clinical trials (patient-facing coordination, data management, regulatory or other research coordination).

Qualifications

• Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills.
• Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences.
• Prior experience in clinical trials is preferred.
• 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.

Skills

• Effective communication skills.
• Good decision-making skills.
• 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.
• Knowledge of regulatory guidelines and following a clinical trial protocol.

Benefits

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. Moffitt 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 Trials Office) Academy.

Pay

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.

Schedule

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.