Global Study Manager II
Parexel
full-time
Posted on:
Location Type: Remote
Location: Pennsylvania • United States
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About the role
- Provides operational leadership throughout the study lifecycle
- Leads and coordinates the execution of a clinical trial globally
- Provides quality oversight and coordination of regional and country operations
- Drives decision making and works closely with the Clinical Study Team Lead
- Ensures development of study level plans
- Approves and oversees drug supply management
- Monitors vendor contracts for out of scope activities and budget spend
- Provides ongoing assessment of subject enrollment
- Serves as technical expert for study management systems and processes
Requirements
- 7+ years of relevant operational clinical trial experience
- Bachelor’s of Science or Bachelor’s of Arts degree
- Master’s of Science or Master’s of Business Administration degree with a minimum 6 years of relevant operational clinical trial experience preferred
- Experience in clinical research and/or study management
- Experience with oversight of CROs and vendors
- Experience in managing per subject costs, vendor and ancillary and monitoring costs projections and spend
- Fluency in written and spoken English required
Benefits
- Health insurance
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial managementstudy managementdrug supply managementvendor contract oversightbudget managementsubject enrollment assessmentoperational leadershipquality oversightCRO oversightcost projections
Soft Skills
decision makingcoordinationcommunicationleadershiptechnical expertise
Certifications
Bachelor’s of ScienceBachelor’s of ArtsMaster’s of ScienceMaster’s of Business Administration