Clinical Research Associate
As a Clinical Research Associate, you will be responsible for conducting site monitoring visits, developing and driving subject recruitment plans, administering protocol training, and evaluating study site practices in accordance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Key Responsibilities:
* Conducting site monitoring visits to ensure compliance with GCP and ICH guidelines
* Developing and implementing subject recruitment plans to meet study enrollment targets
* Administering protocol training to site personnel to ensure understanding of the study protocol
* Evaluating study site practices to identify areas for improvement
Requirements: A Bachelor's Degree in a scientific discipline or healthcare, basic knowledge of clinical research regulatory requirements, good therapeutic and protocol knowledge, computer skills, written and verbal communication skills, organizational and problem-solving skills, and ability to establish and maintain effective working relationships.
About This Role:
This is an exciting opportunity to work in a fast-paced environment and contribute to the advancement of medical knowledge. If you have a passion for clinical research and excellent communication skills, we encourage you to apply.
We Offer:
* A competitive salary and benefits package
* Opportunities for professional growth and development
* A dynamic and supportive work environment