Associate Clinical Research Manager

BeOne Medicines

. Oversee clinical monitoring activities and CRA team performance .

Posted 10/27/2026full-timeRemote • United StatesMid-Level💰 $105,800 - $140,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical monitoring and team management, ensuring compliance with ICH-GCP and local regulations while optimizing processes and supporting trial delivery. Possesses strong interpersonal and organizational skills to effectively lead and mentor CRA teams in the pharmaceutical or CRO industry.

Highest-signal resume keywords

Clinical MonitoringICH-GCP ComplianceTeam ManagementDrug Development ProcessOncology Experience

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

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

Hard Skills

Clinical Monitoring ActivitiesCRA Performance ManagementMonitoring Quality ReviewRisk ManagementProcess OptimizationStudy Milestone SupportIssue Resolution StrategiesSite Compliance AuditsTrial Execution UnderstandingResource Allocation

Soft Skills

Interpersonal SkillsOrganizational SkillsEffective CommunicationMentoringAdaptability

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft Outlook

Industry Keywords

PharmaceuticalCROClinical Research AssociateHealth Authority RequirementsOncology

About the role

Key responsibilities & impact

Oversee clinical monitoring activities and CRA team performance
Ensure compliance with ICH-GCP, local regulations, and company SOPs
Allocate CRA resources and assess workloads to meet study deliverables
Ensure CRAs possess the knowledge and skills required for high-quality monitoring
Manage CRA performance and quality indicators
Strengthen site relationships and support trial delivery
Review monitoring quality and resolve compliance issues
Support study and site milestones with cross-functional teams
Execute assessment visits and accompanied visits when 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, onboard, assign tasks, support, evaluate, mentor, and develop team members
Act as a point of contact for issue escalation and feedback
Address personnel issues promptly and fairly

Requirements

What you’ll need

Bachelor’s degree or higher in a scientific or healthcare discipline
Minimum 5 years of industry experience in the pharmaceutical, 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
Proficient in Microsoft Word, Excel, PowerPoint and Outlook
Fluent in written and verbal English
Adaptable to business trips as required
Valid driver’s license in applicable countries

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 benefits
Professional development opportunities