
Clinical Trial Coordinator Specialist
10 hours ago
This role involves working closely with a team to design and develop calendars, budgets, financials, and case report forms for clinical trial study protocols.
","Key Responsibilities:
","- Interpret clinical trial study protocols to create calendars and site budgets.
- Design and develop case report forms for clinical trial study protocols.
- Collaborate with reporting manager to complete daily/weekly tasks.
Requirements:
","- Knowledge of clinical research methodology, Good Clinical Practice guidelines, and industry regulations.
- Ability to work independently and in a team environment.
- Strong organizational and administrative skills.
Preferred Qualifications:
","- Previous experience in clinical trial coordination or data management.
- Familiarity with MS Office and business software.
As a Research Associate, you will have the opportunity to work on challenging projects and contribute to the success of our organization.
","We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
","Our team is passionate about delivering high-quality results and providing excellent customer service.
","Physical and Mental Requirements:
","- Sitting or standing for extended periods at a workstation.
- Occasional lifting and moving up to 25 pounds.
- Specific vision abilities required.
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