Job Description
As a Senior Clinical Research Associate, you will play a vital role in the success of our clinical trials, driving health outcomes globally. With over 100 countries participating, your dedication to quality and accuracy will make a meaningful impact.
Responsibilities
* Coordinate all aspects of clinical monitoring and site management, ensuring seamless execution.
* Conduct remote or on-site visits to assess protocol and regulatory compliance, managing required documentation efficiently.
* Develop and implement procedures and guidelines from various sponsors and/or monitoring environments.
* Audit sites to ensure compliance with approved protocols, ICH-GCP guidelines, applicable regulations, and SOPs.
Required Skills and Qualifications
* Apply a risk-based monitoring approach to enhance data quality.
* Utilize critical thinking and problem-solving skills to overcome challenges.
* Ensure data accuracy through SDR, SDV, and CRF review.
Why Choose This Opportunity?
This role offers a unique chance to contribute to groundbreaking research and drive innovation in the field of clinical trials. As a Senior Clinical Research Associate, you will have the opportunity to work on diverse projects, develop your skills, and grow professionally.