Clinical Trials Coordinator
3 weeks ago
At ClinLab Staffing, we are seeking a highly motivated and organized Protocol Associate I to join our team.
Key Responsibilities:
- Oversee disease committees in all aspects of protocol development, including concept development, protocol development, NCI and CIRB submissions, quality control reviews, and tracking development timelines.
- Assist with coordinating protocols for review, editing, and formatting for scientific and editorial accuracy.
- Coordinate group-wide notification of study status changes, including activation, suspension, and termination.
- Lead contact for disease chairs, investigators, and senior colleagues.
- Maintain computer databases related to protocol development and status changes.
- Plan and manage monthly teleconferences for assigned disease sites.
- Generate committee tracking documents and prepare high-level notes from teleconferences.
- Participate in departmental meetings, protocol development meetings, and conference calls.
- Interact with other cooperative groups, the NCI, and member coordinators and investigators.
- Prepare concept/LOI packets for submission to the ECOG-ACRIN Executive Committee.
Requirements:
- Exemplary interpersonal, communication, and organizational skills.
- Motivation, organization, and problem-solving skills.
- Ability to manage multiple tasks and meet deadlines.
- Ability to work as part of a team.
- Bachelor's degree in a life science discipline or relevant professional experience.
- Healthcare-related background and prior clinical and/or data services experience.
We offer a dynamic and supportive work environment with opportunities for growth and professional development.
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