About the Role:

We are looking for a Clinical Research Associate to manage clinical trial activities from initiation to closeout. This role involves ensuring trials are conducted in compliance with regulatory standards, monitoring site activities, and ensuring data integrity. The ideal candidate is organized, detail-oriented, and experienced in managing complex clinical trials.

Key Responsibilities:

• Monitor clinical trial sites to ensure protocol adherence and compliance with regulatory standards.
• Assist with site selection, initiation, monitoring, and close-out activities.
• Maintain detailed study documentation and ensure data accuracy and completeness.
• Collaborate with cross-functional teams, including project management and regulatory affairs.
• Mentor junior team members and assist in their professional development (Senior CRA).

Qualifications:

• Bachelor’s degree in Life Sciences or related field; advanced degree preferred.
• Minimum of 2 years (for CRA) or 5 years (for Senior CRA) of clinical research experience.
• Strong knowledge of FDA regulations, ICH guidelines, and GCP.
• Excellent organizational and communication skills.
• Ability to travel for site visits.