Senior/Clinical Research Associate

Responsibilities:

• Oversees study site management to protect patient safety and ensure high-quality data, conducts pre-study, initiation, monitoring, and close-out visits, and prepares accurate monitoring reports.
• Manages site start-up including regulatory submissions and contract negotiations, performs investigational product inventory and reconciliation, and verifies protocol compliance.

Qualifications:

• Requires a Bachelor's degree and a minimum of 2 years of on-site monitoring experience, with proficiency in Microsoft Office, fluency in English, and knowledge of ICH-GCP and the drug development process.
• Must demonstrate strong organizational and interpersonal skills, attention to detail, and the ability to work independently and in a team, with up to 70% travel required.

Company and Culture:

• Precision for Medicine is a CRO focused on integrating clinical trials with deep scientific expertise to improve therapy development speed and success.
• The organization values employee contributions and professional growth, ensuring ideas are nurtured to drive positive change within a collaborative, remote-friendly environment.