Clinical Trial Operations Specialist
13 hours ago
We are seeking a highly skilled Clinical Trial Operations Specialist to join our team. As a key member of the clinical trial management team, you will be responsible for ensuring the timely and accurate delivery of clinical trial activities.
The ideal candidate will have a PhD in Life Sciences and excellent analytical skills. Fluency in English is required, as well as the ability to work in a fast-paced dynamic environment. Prior experience in the CRO or pharmaceutical industry is advantageous but not necessary.
This is an exciting opportunity for recent graduates or professionals looking to transition into a career in clinical trials. You will receive comprehensive training and support to develop your skills and advance your career.
Key Responsibilities:
- Communicate and collaborate with global study teams
- Ensure timely delivery of recurrent tasks with high accuracy
- Compile and maintain project-specific status reports
- Interact with internal project teams, sponsors, and third-party vendors
What We Offer:
- Competitive salary: $65,000 - $85,000 per annum
- A comprehensive benefits package
- A flexible work environment
- Structured career paths with opportunities for professional growth
About Us:
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
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