Senior Clinical Research Associate Job Description
We are seeking a highly skilled Sr. CRA I/II to join our team.
* Main Responsibilities:
* Perform site qualification, initiation, monitoring, management, and close-out visits to ensure compliance with regulatory requirements.
* Evaluate site performance and provide recommendations for improvement.
* Stay up-to-date with ICH/GCP guidelines and company SOPs.
The Ideal Candidate:
* Verifies informed consent processes and maintains confidentiality.
* Assesses factors affecting subject safety and data integrity.
* Conducts source document review and resolves queries remotely and on-site.
We Offer:
* A dynamic work environment with opportunities for growth and development.
* Competitive compensation and benefits package.
* Collaborative team atmosphere.
About Us:
* We are a leading biopharmaceutical solutions organization dedicated to accelerating customer success.