Senior Clinical Operations Assistant
Primary Location: Romania, Bucharest 求人ID R0000043283 Category Clinical Trials
About this Role
Parexel is a leading clinical research organization dedicated to advancing life-changing medicines. We work with the world's most innovative companies to bring new treatments to patients who need them. If you're passionate about quality, precision, and making a real difference in clinical research, we want to
As a Senior Clinical Operations Assistant (SCOA), you'll be the backbone of our clinical teams, ensuring the smooth execution of clinical trials through meticulous administrative excellence. You'll manage critical documentation, coordinate site activations, process payments, and provide essential support to our clinical teams—all while maintaining the highest standards of quality and compliance.
This is a role for someone who thrives on organization, attention to detail, and supporting others to succeed. You may also have the opportunity to lead COA teams on large studies and participate in company-wide initiatives.
This role offers flexible working arrangements with a mix of office and home working.
Key Responsibilities:
Trial Master File Management
Track, scan, code, and organize documents according to the Trial Master File Plan. Maintain quality checks, manage document transfers, and ensure compliance with regulatory requirements.
Site Activation & Support
Coordinate vendor management for system access (EDC, IVRS), organize investigator site files, and provide comprehensive training support to site staff.
Payment Processing
Review site contract compliance, process invoices, coordinate with finance teams, and ensure timely and accurate site payments.
Clinical Team Support
Manage CTMS and study trackers, coordinate document translations, handle courier shipments, track recruitment initiatives, and support data cleaning activities.
Essential Skills & Experience:
Previous experience in Clinical Trials
Strong computer proficiency with CTMS, EDMS, Excel, and Word
Knowledge of ICH-GCP guidelines and clinical trial regulations
Experience in office management in an international environment
Excellent written and verbal communication skills
Ability to manage multiple tasks and prioritize effectively
High attention to detail and commitment to quality
Problem-solving mindset with the ability to work independently
Why Join Parexel?
Parexel is a leading global clinical research organization with a commitment to advancing clinical research and improving patient outcomes.
We offer:
Work in a collaborative, supportive environment with experienced clinical professionals
Flexible work arrangements
Career growth opportunities within a global organization.
If you are ready to join Parexel’s Journey, please apply!
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