Associate Clinical Research Manager

BeOne Medicines

. Oversee clinical monitoring activities and CRA team performance .

Posted 9/18/2026full-timeRemote • United StatesJuniorMid-Level💰 $105,800 - $140,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical monitoring and team leadership, ensuring compliance with ICH-GCP and local regulations while optimizing trial execution and performance. Proficient in managing CRA resources, conducting performance evaluations, and fostering team development in a pharmaceutical or CRO environment.

Highest-signal resume keywords

ICH-GCP ComplianceClinical MonitoringTeam LeadershipDrug Development ProcessOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical MonitoringCRA Performance ManagementProcess OptimizationRisk ManagementMonitoring Quality ReviewStudy Milestone DeliveryResource AllocationPerformance EvaluationIssue ResolutionTrial Execution

Soft Skills

Interpersonal SkillsOrganizational SkillsEffective CommunicationMentoringCollaboration

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft Outlook

Industry Keywords

PharmaceuticalCROHealth Authority RequirementsSite Compliance VisitsOncology

About the role

Key responsibilities & impact

Oversee clinical monitoring activities and CRA team performance
Ensure compliance with ICH-GCP, local regulations, and company SOPs
Lead the CRA team to achieve organizational goals and high performance
Allocate CRA resources and assess workload to meet study deliverables
Ensure CRAs have the monitoring knowledge and skills needed to perform activities with high quality
Manage CRA performance and quality indicators
Strengthen site relationships to enhance performance and trial delivery
Review monitoring quality and resolve compliance issues
Support study and site milestone delivery with cross-functional teams
Execute assessment visits and accompanied visits where required
Identify issues and develop resolution strategies
Contribute to process optimization and manage risk escalation and resolution
Support site audits, inspections, and Site Compliance Visits
Ensure corrective action and follow-up for identified issues
Recruit, hire, and onboard team members
Assign tasks based on individual strengths and team objectives
Provide team members with resources and support
Encourage communication and collaboration within the team and with other functions
Conduct performance evaluations and provide constructive feedback
Mentor team members and support their professional development
Address personnel issues promptly and fairly

Requirements

What you’ll need

Proficient in Microsoft Word, Excel, PowerPoint and Outlook
Fluent in written and verbal English
Minimum 5 years of industry experience in the pharmaceutical or CRO or relevant field
Thorough understanding of the drug development process
Expert knowledge of international standards (ICH-GCP) and health authority requirements
Understanding of all aspects of monitoring and trial execution
Previous experience as a CRA preferred
Excellent interpersonal skills
Strong organizational skills
Effective written and verbal communication skills
Experience in Oncology highly recommended
Adaptable to business trips as required per business need
Valid driver’s license in applicable countries
Bachelor’s degree or higher in a scientific or healthcare discipline
Advanced degrees preferred

Benefits

Comp & perks

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