Lead Clinical Research Associate
Drive innovation and excellence in clinical research by serving as a key player in our sponsor-dedicated team.
About the Role
* We are seeking an experienced Lead Clinical Research Associate to conduct site selection, initiation, monitoring, and close-out visits with precision and purpose.
Key Responsibilities
* Develop subject recruitment strategies that deliver results and keep studies on track.
* Deliver protocol training and build strong relationships with site teams.
* Ensure compliance with GCP/ICH standards and escalate issues when necessary.
* Track study progress, manage documentation, and maintain Trial Master Files audit-ready.
* Mentor junior clinical staff and foster a culture of excellence and learning.
* Collaborate with cross-functional teams for seamless project execution.
Requirements
* Bachelor's degree in a scientific or healthcare discipline (or equivalent experience).
* 5+ years of independent on-site monitoring experience, with 3+ years in oncology.
* Deep knowledge of GCP, ICH, and clinical trial regulations.
* Strong therapeutic area expertise and protocol understanding.
* Tech-savvy with Microsoft Office and mobile tools.
* Excellent communication, organization, and problem-solving skills.
* A proactive mindset and ability to build strong stakeholder relationships.