Global Study Coordinator
4 days ago
We are seeking a highly skilled Clinical Research Coordinator to join our team at Vitalief.
Key Responsibilities
- Perform various research operations for assigned observational clinical studies.
- Implement quality control SOPs, conduct monitoring visits, and develop protocols with investigators.
- Establish standard operating procedures and manuals for clinical studies.
- Train junior research assistants in study document preparation and protocol implementation.
Requirements and Qualifications
- Bachelor's Degree or Master's Degree with relevant experience.
- Experience overseeing protocols, translating them into operational implementation, and conducting international site visits.
- Excellent relationship building, interpersonal, and communication skills.
- Organizational skills, attention to detail, and computer literacy.
Work Location and Travel Requirements
- 100% remote job, but candidates must reside in NY, NJ, CT, or PA.
- Ability to travel internationally up to 30% for site visits and meetings.
Benefits
- Estimated salary range: $65,000 - $73,000 depending on experience.
- 20 PTO days plus 9 paid Holidays annually.
- Company-paid life insurance, short/long-term disability coverage, 401K retirement program, and robust healthcare plans.
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