Senior Clinical Research Associate
BeOne Medicines
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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Job Level
About the role
- Complete appropriate therapeutic, protocol and clinical research training/CRA training to perform job duties.
- Perform site selection and evaluation, supporting initial list of sites and recruitment targets.
- Conduct onsite/remote pre-study, initiation, routine monitoring and closeout visits per monitoring plan.
- Create and maintain documentation regarding site management and monitoring visit findings.
- Ensure inspection readiness of the study and sites.
- Collaborate with Country and Regional Clinical Study Managers to ensure timely delivery of study milestones.
- Mentor junior staff (Associate CRA and CRA) and act as the escalation point person for CRA(s) with site-related issues.
Requirements
- BS in a scientific or healthcare discipline preferred and at least 3 - 5 years of monitoring experience
- Advanced knowledge of applicable clinical research regulatory requirements
- Experience in oncology/onco-hematology global trials preferred
- Excellent communication and interpersonal skills
- Ability to establish and maintain effective working relationships
- Excellent organizational and problem-solving skills
- Computer Skills: Efficient in Microsoft Word, Excel, PowerPoint, Outlook
Benefits
- Professional development opportunities
- Health insurance
- Flexible working arrangements
- Paid time off
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchmonitoringsite selectionprotocol trainingregulatory requirementsoncology trialsonco-hematology trialsdocumentation managementproblem-solving
Soft Skills
communicationinterpersonal skillsorganizational skillsrelationship buildingmentoringleadership