Clinical Site Specialist
Vor 7 Tagen
Transforming Healthcare Through Innovation
Parexel is seeking a Clinical Site Monitor I or II to join our team. As a home-based Clinical Site Monitor, you will play a critical role in ensuring data integrity and quality, and ensuring compliance with ICH GCP and local regulations at the site level.
The successful candidate will be responsible for monitoring data quality and integrity, and will collaborate with the Site Manager to ensure that the site follows the protocol and is inspection-ready. You will also coordinate with institutions and investigators at the local level, and utilize systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), and electronic Investigator Site File (eISF).
Key Responsibilities:
- Ensure data integrity and quality
- Collaborate with Site Manager to ensure protocol compliance
- Coordinate with institutions and investigators
- Utilize CTMS, eTMF, and eISF systems
Requirements:
- A minimum of 1 year experience as a Clinical Research Associate
- Oncology trials experience
- Experience in utilizing CTMS, eTMF, and eISF systems
- Bachelor's degree or Registered Nurse (RN) in a related field
We Offer:
- Exceptional financial rewards
- Training and development opportunities
- A healthy work-life balance
About Us:
Parexel is a global biopharmaceutical company that relentlessly seeks breakthroughs to improve patients' lives. Our daily innovation contributes to a healthier global community.
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