Job Overview
Location
Germany-Berlin-Remote
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 16, 2026
Full Job Description
đź“‹ Description
- • Senior Clinical Research Associate role focused on ensuring patient safety and quality execution of clinical trials for a major sponsor in the EU, contributing to the development of therapies that benefit patients worldwide.
- • Day-to-day responsibilities include managing site activation, monitoring, and close-out activities; ensuring compliance with Study Monitoring Plans, ICH/GCP, and regulatory requirements; tracking adverse events; interfacing with study teams, vendors, and investigator sites; and supporting audit readiness and CAPA processes.
- • Parexel is a global leader in clinical research, supporting trials for many of today’s top-selling drugs and enabling critical niche therapies across therapeutic areas, with a mission to improve global health through empathy-driven, patient-centered work.
- • In this role, you will deepen your expertise in oncology-focused clinical monitoring, strengthen cross-functional collaboration skills, and play a pivotal role in bringing safe, effective therapies to patients while growing within a purpose-driven organization.
🎯 Requirements
- • Bachelor’s degree in life sciences or equivalent professional background (e.g., nursing, pharmacy, medical)
- • Minimum 3.5 years of relevant experience in clinical research site monitoring, preferably in Oncology
- • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA, and local country regulations
🏖️ Benefits
- • Opportunity to contribute to meaningful patient outcomes through impactful clinical trial work
- • Engagement with a global leader in clinical research supporting top-tier drug development
- • Collaboration within a dedicated, mission-driven team focused on improving world health
Skills & Technologies
About Parexel International Corporation
Parexel provides global biopharmaceutical services, managing Phase I-IV clinical trials, regulatory consulting, market access, and real-world evidence studies for drug and device development. The company supports sponsors in trial design, site selection, patient recruitment, data management, biostatistics, pharmacovigilance, and health economics. Operating in over 100 countries, Parexel integrates therapeutic expertise with technology platforms to accelerate approvals and improve evidence generation. Services span oncology, neurology, rare diseases, and vaccines, combining decentralized trial capabilities, digital health tools, and post-marketing surveillance to optimize development timelines and commercial success.
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