Senior Clinical Research Associate

Responsibilities

• Schedule and conduct pre-study, initiation, interim monitoring, and close-out visits according to the Monitoring Plan.
• Ensure HGRAC and IRB submissions and approvals are obtained.
• Verify that assigned sites conduct studies in compliance with protocols, applicable regulations, and guidelines.
• Protect the rights and wellbeing of human subjects throughout the clinical trial.
• Ensure trial data is accurate, complete, and verifiable from source documents.
• Perform source document verification against Case Report Forms and Electronic Data Capture entries.
• Manage Investigational Product accountability, including storage, inventory, and dispensing records.
• Communicate protocol or GCP deviations to investigators and project management teams.
• Deliver high-quality written reports and follow-up letters within established timelines.
• Participate in site audits and conduct site feasibility assessments as required.

Requirements

• Bachelor's or Master's degree (or equivalent university degree).
• At least 3 years of CRA experience within a multinational pharmaceutical company, Medical Device company, or CRO.
• Proven experience with Medical Device or IVD clinical trials.
• Strong knowledge of clinical trial Quality Management Systems (QMS).
• Fluency in English with strong communication skills.
• Academic background in clinical medicine, pharmacy, or pathology.
• Ability to travel domestically (approximately 10% of the time).

About the Company

Agilent is a global leader in laboratory and clinical technologies, dedicated to bringing great science to life. With over 50 years of expertise and 18,000 employees worldwide, we provide advanced instruments, software, and consumables that support life science research, patient diagnostics, and environmental safety. Our culture is built on trust, respect, and integrity, fostering an inclusive workplace where innovation drives meaningful impact in human lives.