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Clinical Trials Coordinator
1 month ago
We are seeking a highly skilled Clinical Trials Coordinator to join our team at Dana-Farber Cancer Institute. As a key member of our clinical trials team, you will be responsible for effective and efficient scheduling of clinical trial or protocol patients and/or transplant donors for clinical services and other resources.
Key Responsibilities:
- Carry out specialized tasks to support regulatory requirements and patient safety, requiring an understanding of the sequential processes involved in clinical trials and patient treatment plans.
- Order and ensure or carry out the shipping and tracking of lab tests or samples as required.
- Participate in continuous training and maintain current knowledge of the clinical process, regulatory standards, and requirements that impact the assigned patient population.
- Responsible for ensuring filing or reporting of certain documentation, including patient records, protocol records, quality control and quality assurance reports.
- Maintain proficiency in operating multiple clinical information systems applications.
Requirements:
- Demonstrated ability to work in highly regulated environments, such as clinical trials or complex medical systems.
- Ability to manage complex projects through to completion.
- Proficient with Microsoft Office products and knowledge of electronic medical records system and GE_IDX preferred.
- Ability to work productively in a remote environment.
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and detail-oriented individual who is passionate about delivering exceptional patient care, we encourage you to apply for this exciting opportunity.