Clinical Trials Screening Coordinator I - GI

Responsibilities

• 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
• This is role is within the clinical trials career path supporting the PI in clinical trials

Preferred

• Prior experience in clinical trials is preferred

Benefits

• Monday through Friday schedule
• Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period
• Paid training and orientation through its CTO (Clinical Trials Office) Academy
• Relocation assistance may be provided
• Glassdoor
• 3.9
• Comprehensive cancer hospital and research center.
• Tampa, Florida, USA
• http://moffitt.org
• Late Stage
• Total Funding
• $0.01M
• Key Investors
• Foundation Medicine
• MassMutual Foundation
• 2023-07-31
• Grant
• 2023-07-12
• Grant· $0.01M
• Leadership Team
• Joanna Weiss
• Chief Financial Officer
• Timothy Yeatman
• Executive Vice President, Founding Chief Scientific Officer
• Recent News
• BioSpace
• Anixa Biosciences Announces First Case of Stable Disease for Three Months in Ovarian Cancer CAR-T Clinical Trial
• 2026-10-06
• Morningstar.com
• Cizzle Bio Highlights CIZ1B Biomarker Blood Test for Lung Cancer at Next Generation Dx Summit

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
• 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
• 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)
• Prior experience in clinical trials is preferred
• 2 years' experience in clinical trials (patient-facing coordination, data management, regulatory or other research coordination).

Required skills

• Clinical Trials, Clinical Research Regulatory Requirements, Clinical Trial Protocols, Patient Care Coordination

Preferred skills

• Prior experience in clinical trials is preferred

Experience

• 2+ years