Senior Clinical Research Associate – BD Nogales Norte
Job 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. Travel of approximately 60% of the time is required, mainly within Europe.
Main Responsibilities
* 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.
Qualifications
* 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 is beneficial.
* Strong analytical and communication skills with fluency in English.
Salary
€54,800.00 – €93,200.00 EUR Annual
Location
BD Nogales Norte (travel within Europe)
Equal Opportunity Statement
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.
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