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Job Description Summary
This position plays a key role in managing the day‑to‑day activities of clinical studies from initiation through close‑out. The Senior Clinical Research Associate ensures that all site‑level activities comply with applicable regulations, Good Clinical Practice, company standards and procedures. The role involves planning and conducting monitoring visits, ensuring data quality, participant safety, and compliance, while also providing leadership and mentoring within the clinical research team. You will be expected to travel around 60% of your time, mainly within Europe.
OUR VISION FOR BDB AT BD
BD Biosciences (BDB) is a leading provider of high‑quality flow cytometry and single‑cell genomics solutions, scientific research and clinical laboratories. Here, we are leading the way by developing the best technologies that have the ability to look closer at the details of cells and diseases.
Why join us?
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth‑centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Main Responsibilities Will Include
* Plan and deliver site management and monitoring activities within timelines and budget.
* Track and report study progress, including data collection, cleaning, and site performance.
* Conduct on‑site and remote monitoring visits, ensuring accurate documentation and compliance.
* Prepare and maintain study documentation, including monitoring plans, reports, and site files.
* Review site performance data to identify risks and develop corrective actions where needed.
* Support training for investigators, study staff, and junior team members.
* Act as the primary contact for study sites and coordinate with internal teams and vendors.
* Contribute to continuous improvement initiatives and support audits or inspections.
About You
* Bachelor’s degree in a healthcare or scientific field, or equivalent experience.
* Minimum five years of experience in a similar position with hands‑on site monitoring.
* Understanding of ICH‑GCP, ISO standards, and regional regulations related to clinical research.
* Proficiency in using clinical trial management systems such as EDC, CTMS, and eTMF.
* Knowledge of BD instruments and reagents would be beneficial.
* Strong analytical and communication skills with fluency in English.
Click on apply if this sounds like you!
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally‑protected characteristics.
To learn more about BD visit: https://bd.com/careers
Salary Range Information
€54,800.00 – €93,200.00 EUR Annual
Seniority level
* Mid‑Senior level
Employment type
* Full‑time
Job function
* Research, Analyst, and Information Technology
Industries
* Medical Equipment Manufacturing
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