Senior Clinical Research Associate (Project Lead)

Overview :

Revvity is seeking a Senior Clinical Research Associate (Sr. CRA) to support global In Vitro Diagnostic (IVD) clinical trials. This role goes beyond traditional monitoring as you will be involved in the full lifecycle of clinical studies, including site startup, monitoring, data oversight, and preparation for regulatory submissions.

The ideal candidate is a hands-on clinical research professional who thrives in a multi-hat role : part CRA, part study coordinator, and part project contributor. You will have the opportunity to work across diverse diagnostic programs within a global Clinical Affairs team, supporting studies that directly impact patient care worldwide.

Why Join Revvity :

At Revvity, you will be part of a lean, high-impact global Clinical Affairs team driving the development of diagnostic solutions that improve patient care worldwide. This position offers the chance to step beyond traditional monitoring and gain broad exposure to regulatory submissions, data management, and study planning. Your contributions will be visible, valued, and essential to advancing our mission.

Key Responsibilities :

Clinical Study Execution

Contribute to study planning, feasibility, and protocol development

Identify, evaluate, and activate clinical trial sites

Support contract and budget coordination during site startup

Serve as a primary point of contact for site staff throughout the study

Monitoring and Oversight

Conduct site qualification, initiation, interim monitoring, and close-out visits Ensure compliance with protocol, ICH-GCP, FDA, and applicable local and global regulations

Verify informed consent and assent processes and patient protections, including pediatric populations

Apply risk-based monitoring strategies and escalate issues when needed

Data Quality and Reporting

Perform source document verification, CRF and eCRF review, and query resolution

Monitor study databases for accuracy, completeness, and data integrity

Collaborate with data management and biostatistics teams to resolve discrepancies

Cross-Functional Collaboration

Work closely with Global Clinical Affairs colleagues, regulatory, and operations teams to support study deliverables

Provide input into study documents and clinical operations planning

Basic Qualifications :

• Bachelor’s degree in a scientific or healthcare field or RN / BSN AND a minimum 5 years of clinical research experience including independent monitoring AND
• Experience in Type 1 Diabetes, infectious diseases, or newborn screening clinical studies AND in Vitro Diagnostic (IVD)

Preferred Qualifications :

The base salary range for this full-time position is $102,500.00 - $128,000.00. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.

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What do we offer?

We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits :

Learn more about Revvity’s benefits by visiting our page. Log-In instructions are provided towards the bottom of the Bswift page.

For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information.