Clinical Study Start Up Project Coordinator

📋 Description

• Review research protocols, consent documents, and manuals to extract pertinent information for developing resources for the clinical team.

• Create and configure clinical research documentation.

• Use study startup documents to initiate the creation of therapeutic EMR treatment plans.

• Collaborate with the Principal Investigator, clinical staff, and pharmacy to gather requirements and ensure that documentation and treatment plans align with clinical needs.

• Draft and distribute Letters of Collaboration across multiple departments as required.

• Troubleshoot and resolve issues related to clinical documents, treatment plans, and Letters of Collaboration.

• Maintain all documentation distributed to the clinical team.

• Attend departmental meetings involving regulatory and pharmacy teams.

• Undertake additional responsibilities as needed.

⛳️ Requirements

• A bachelor's degree in a relevant field is required.

• Strong knowledge of clinical research workflows and protocol understanding.

• Excellent written and verbal communication abilities.

• Proficiency in Microsoft Office Suite.

• Outstanding attention to detail and organizational skills.

• Capability to work independently, juggle multiple projects, and meet deadlines.

• A minimum of two years of clinical research-related experience is preferred.

🏝️ Benefits

• Comprehensive health insurance coverage.

• Opportunities for professional development and training.

• Flexible work schedules and remote work options.

• Competitive salary and performance bonuses.