Senior Clinical Research Associate
Jordan Griffiths is working with a global CRO, which is currently seeking a Senior Clinical Research Associate to join their team. As a Senior CRA, you will play a vital role in the execution and monitoring of clinical trials, ensuring compliance with protocols and regulatory requirements.
Key Responsibilities:
- Conduct site initiation, monitoring, and
- out visits - Ensure compliance with study protocols, GCP, and applicable regulatory guidelines
- Perform source data verification and review study documents
- Track and report patient enrollment and study progress
- Monitor study drug supply and accountability
Requirements
- Bachelor's degree in life sciences or related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Strong knowledge of GCP and regulatory requirements.
- Excellent communication and organizational skills.
- Ability to travel to sites as necessary.
Benefits
- Competitive salary & benefits.
- Clear progression plans in place.
- Work with leading technology.
- Be part of a global leader in clinical research with a strong commitment to innovation and quality.
- Work on
- edge clinical trials that impact patient lives around the world.
- Enjoy a supportive and collaborative work environment with opportunities for professional growth and development.
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