Clinical Study Start Up Project Coordinator

Job Description

We are seeking a Clinical Study Start Up Project Coordinator to manage clinical documents and treatment plans within a clinical research setting. The coordinator will: - Review study protocols, consent forms, and manuals to extract relevant information for the clinical team. - Develop and configure clinical research documentation. - Utilize study start up documents to initiate therapeutic EMR treatment plan creation. - Collaborate with Principal Investigator, clinical staff, and pharmacy to gather requirements and ensure documentation and treatment plans meet clinical needs. - Create and distribute Letters of Collaboration with multiple departments as needed. - Troubleshoot and resolve issues related to clinical documents, treatment plans, and Letters of Collaboration. - Maintain all documentation dispersed to the clinical team. - Participate in departmental meetings with regulatory and pharmacy. - Perform additional responsibilities as necessary.

Qualifications

1. Completion of a bachelor’s degree in a relevant field. 2. Strong understanding of clinical research workflow and protocol comprehension. 3. Excellent written and verbal communication skills. 4. Proficiency in Microsoft Office Suite. 5. Exceptional attention to detail and organizational skills. 6. Ability to work independently, manage multiple projects, and meet deadlines. 7. Two years of clinical research-related experience preferred.