Philips Senior Clinical Research Associate 

United States 

837520616

Senior Clinical Research Associate

Your role:

• In this role, you'll contribute directly to the success of international post-market clinical investigations by ensuring site performance, safety, and regulatory compliance.

• You’ll collaborate closely with Clinical Study Managers, investigators, and cross-functional teams to ensure studies are conducted to the highest standards.

• This role offers opportunities for professional development through global exposure, autonomy in execution, and collaboration with world-class clinical teams. Remote work and limited travel may be required.

• Lead monitoring activities across global study sites, including start-up, site assessments, monitoring visits, and closeouts.

• Author and review clinical documentation such as study protocols, informed consents, and reports in alignment with regulatory and Good Clinical Practice (GCP) standards.

• Support training and guidance for investigators and internal stakeholders on clinical protocol requirements and regulatory expectations. Utilize and maintain trial management tools such as EDC, eTMF, and CTMS with a high level of competency.

• Oversee site management activities, including contract and budget negotiations, document collection, and regulatory submissions. You will also Contribute to the optimization of study processes, ensuring data integrity, protocol compliance, and continuous improvement in clinical operations.

You're the right fit if:

• You’ve acquired 2+ years of experience in clinical research, including at least 2 years as a Clinical Research Associate—ideally within Class III medical devices—or you bring a background in emergency care as a first responder or nurse with experience in an ER setting.

• Your skills include some regulatory compliance, knowledge of ISO 14155, FDA, ICH/GCP, medical terminology (cardiovascular preferred), and proficiency in EDC, eTMF, and CTMS systems.

• You have a Bachelor’s or Master’s degree in Life Sciences or Nursing; clinical background in Emergency Department, ICU, CCU, CVOR, or Cath Lab preferred.

• You’re an excellent communicator with a collaborative mindset and the ability to work independently under minimal supervision. Clinical Research certification (SOCRA or ACRP) is a plus.

• You’re experienced in post-market clinical trials or registries in the U.S., EU, Australia, or other international markets.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

How we work together

This is an Field role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The pay range for this position in AZ, AR, ID, IA, KS, KY, LA, ME, MS, MO, NE, NM, OK, SC, SD, TN, UT, or WV is $96,188 to $153,900

The pay range for this position in AL, CO, FL, GA, HI, IL, IN, MI, MN, NV, NH, NC, ND, OH, OR, PA, TX, VT, VA, WI, or WY is $101,250 to $162,000

The pay range for this position in AK, DE, MD, NY, RI, or WA is $106,313 to $170,100

The pay range for this position in CA, CT, DC, MA, or NJ is $113,400 to $181,440

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.