Senior Clinical Research Associate

Senior Clinical Research Associate

Location: Diegem (hybrid)

Duration: Until Jan 31, 2027

Hours: 40

Imagine your next project overseeing clinical trials that are critical to bringing life-saving medical devices to patients in need.

You will be responsible for managing clinical activities at study sites conducting studies for the MedTech group, as well as fostering strong, productive relationships with colleagues within the MedTech Group. You will verify the safety and well-being of study subjects and ensure the collection of high-quality, substantiated data.

roles and responsibilities.

In this role, you will be responsible for managing clinical study activities for multiple sites in single or several clinical projects.

This will involve:

• Verify safety and well being of study subjects are maintained for assigned study sites

• Support the operational execution of clinical trials and ensure collection of high quality, substantiated data

• Execute clinical trials activities following established standard operating procedures, good clinical practices and regulatory requirements

• Accountable for study site performance, and providing high quality data according to overall project timeline

• Assist Clinical Operations staff and study site staff to quickly and effectively resolve issues

• Verify Investigator Site Files at assigned study sites are maintained according to regulations and/or company requirements/procedures

• Responsible for supporting patient recruitment and retention activities

• Performs site visits and ensures study site is compliant with the study protocol and all Federal, State, local, and company regulations

• Interface and collaborate with Investigators, IRBs/ECs, contractors/vendors, and company personnel as needed

how to succeed.

To succeed in this role, you should have a strong understanding of clinical research regulations and the ability to travel up to 80% of the time.

You will also bring:

• 4+ years in Site Monitoring & Medical Devices

• Previous clinical research experience required

• Previous medical device monitoring or equivalent experience required

• Relevant industry certifications preferred (i.e., CCRA, RAC, CDE)

• Experience and knowledge working with computer systems (Microsoft Office – Excel, Word, and Power Point)

• Strong organizational skills and the ability to manage multiple sub-projects

benefits.

This role offers a very competitive hourly rate. This contract will run until Jan 31, 2027.

you are welcome here.

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson MedTech

At Johnson & Johnson MedTech, we unleash diverse healthcare expertise, purposeful technology, and a passion for people to transform the future of medical intervention and empower everyone to live their best life possible.

application process.

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”