Clinical Trials Coordinator
3 weeks ago
The Clinical Trials Coordinator 2 will work collaboratively within a multidisciplinary clinical/research team to ensure timely and accurate execution of all aspects of patient management. The incumbent must be comfortable working independently, managing interactions with and between team members, both internally and externally, to ensure high-quality management of NIH grant-funded, industry-sponsored, or investigator-driven studies/trials. The incumbent will promote improved access for patients to clinical trials and facilitate research activities throughout LSUHSC-affiliated clinics and partner hospitals as assigned. The incumbent will also prepare and edit clinical study protocols and scientific documents.
Key Responsibilities
- Collaborate with a multidisciplinary clinical/research team to ensure timely and accurate execution of all aspects of patient management.
- Manage interactions with and between team members, both internally and externally, to ensure high-quality management of NIH grant-funded, industry-sponsored, or investigator-driven studies/trials.
- Promote improved access for patients to clinical trials and facilitate research activities throughout LSUHSC-affiliated clinics and partner hospitals as assigned.
- Prepare and edit clinical study protocols and scientific documents.
Requirements
- Bachelor's degree in biological sciences, healthcare, or a related field from an accredited institution.
- CCRC or CCRP certification.
- Three years of research or clinical trial experience in a hospital/clinic/academic setting.
Preferred Qualifications
- Master's degree in biological science, healthcare, or a related field.
- Five years of research and/or clinical trial experience.
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