Regional Clinical Trial Management Associate

BeOne Medicines

. Support the Regional Clinical Study Manager in regional study delivery and delegated clinical study components .

Posted 10/9/2026full-timeRemote • United StatesJuniorMid-Level💰 $72,800 - $97,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research operations, including study delivery, regulatory compliance, and document management. Proficient in utilizing clinical trial management systems and supporting cross-functional teams in the execution of clinical studies.

Highest-signal resume keywords

Clinical Research ExperienceKnowledge of Clinical Operations MethodologiesMS Office ProficiencyETMF ManagementCTMS Utilization

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ConductFeasibility AssessmentDocument GenerationSample TrackingParticipant EnrollmentQuality ControlOperational Risk IdentificationVendor SetupBudget ManagementData Cleaning

Soft Skills

Team CollaborationCommunication SkillsOrganizational SkillsProblem-Solving

Tools & Technologies

CTMSETMFSharePoint

Industry Keywords

BiotechPharmaCROICH GuidelinesSOPs

About the role

Key responsibilities & impact

Support the Regional Clinical Study Manager in regional study delivery and delegated clinical study components
Support Clinical Research Associates and Study Start-up Specialists in country study delivery
Support clinical trial conduct, including feasibility assessment, study start-up, document generation and review, sample tracking, and participant enrollment
Support CTMS updates, ISF binder preparation, document collection, ICF customization, and eTMF maintenance
Interpret and implement regulations and ICH guidelines
Set up regional and country team meetings, agendas, and minutes
Maintain SharePoint folders, distribution lists, eTMF, CTMS, and other study systems
Support system access requests and user account management
Support study start-up, investigator meetings, TMF creation, review, and quality control
Help resolve regional or country clinical supply issues and support data cleaning
Prepare site newsletters and clinical trial correspondence
Support public registry information maintenance and Clinical Study Report inputs
Support operational risk identification, audits, inspections, tools, work instructions, and SOPs
Support vendor setup, regional study budgets, purchase orders, payments follow-up, and accrual activities

Requirements

What you’ll need

1 or more years of experience in clinical research within biotech, pharma or CRO industry
Knowledge of clinical operations methodologies and understanding of operational aspects of clinical study processes
MS Office, eTMF, CTMS
Preferably Bachelor’s Degree, preferably in a scientific or healthcare discipline required
Limited travel might be required
Exceptions might be made for candidates with relevant clinical operations experience

Benefits

Comp & perks

Annual bonus plan eligibility for non-commercial roles
Incentive compensation plan eligibility for commercial roles
Discretionary equity awards
Voluntary Employee Stock Purchase Plan participation
Medical
Dental
Vision
401(k)
FSA/HSA
Life Insurance
Paid Time Off
Wellness