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BeOne Medicines

Senior Regional Clinical Trial Management Associate

BeOne Medicines

Supports the Regional Clinical Study Manager in ensuring quality clinical trials delivery. Collaborates with teams on study area operations, supporting multiple aspects of clinical trials.

Posted 7/29/2026full-timeRemote • 🇫🇷 FranceSenior💰 €53,600 - €67,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical research and operations, with a strong focus on supporting regional study delivery and collaboration with key stakeholders. Proficient in overseeing clinical trial conduct and reviewing study-related documents.

Highest-signal resume keywords
Clinical Research ExperienceClinical Operations MethodologiesStudy ManagementCollaboration SkillsMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical ResearchClinical Trial ConductStudy Document ReviewRegional Study ManagementOperational Aspects of Clinical Studies
Soft Skills
CollaborationCommunication
Certifications & Qualifications
Bachelor’s Degree in Scientific Discipline
Industry Keywords
BiotechPharmaCROClinical Study Processes

About the role

Key responsibilities & impact
  • Supports the Regional Clinical Study Manager in regional study delivery
  • Supports the alignment of regional deliverables with overall study goals
  • Develops regional study management experience by supporting to oversee multiple aspects of clinical trial conduct
  • Establishes good collaboration with Regional Clinical Study Manager, Global Study Management Associate, and other key stakeholders
  • Assists in the review of study-related documents as delegated by the Regional Clinical Study Manager
  • Supports the organization of study-specific investigator meetings

Requirements

What you’ll need
  • Bachelor’s Degree in a scientific or healthcare discipline required
  • 2 + years of experience in clinical research within biotech, pharma or CRO industry
  • Knowledge of clinical operations methodologies, understanding of operational aspects of clinical study processes
  • Computer Skills: MS Office

Benefits

Comp & perks
  • Health insurance
  • Professional development