Global Study Manager II

Parexel

Global Study Manager providing leadership for clinical trials at Parexel. Ensuring compliance, budget oversight, and successful trial delivery across multiple countries.

Posted 4/22/2026full-timeRemote • 🇵🇱 PolandMid-LevelSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide leadership and direction to the trial team
Accountable for the overall success and delivery of their assigned clinical trial according to defined milestones and KPI’s
Responsible for steering and directing clinical trial activities
Direct communication and interaction with multiple internal and external stakeholders
Ensure trial team members are aligned and on track for trial timelines
Supports development of trial level documents owned by other functions
Verifies and provides input into the country allocation and oversees trial feasibility
Maintains oversight during clinical trial conduct including adherence to GCP and all regulatory requirements
Ensures budget oversight in collaboration with other functions
Prepare and implement amendments of core documents
Support authority/ethics response as applicable
Ensures timely cleaning and delivery of clinical trial data
Coordinates and supports trial medical writer in providing the CTR
Responding for timely, complete and compliant archiving of all relevant global documents

Requirements

What you’ll need

Bachelor’s degree and minimum 6 years of relevant global study management/leadership experience
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
Ability to work outside of core business hours, as required, to support global trials or initiatives
Ability to travel, as required, including IMs, vendor kick off and re-set meetings, and client internal global or department level meetings
Technical proficiency in trial management systems and MS applications, including but not limited to Teams, MS Office, Project, CTMS, EDC, IWRS/IVRS.
Knowledge of ICH GCP and relevant regulatory guidelines/directives.
Demonstrated interpersonal & leadership skills.
Ability to understand and implement the strategic direction and guidance for respective clinical studies.
Effective communication skills via verbal, written and presentation abilities.

Benefits

Comp & perks

health insurance
retirement plans
paid time off
flexible work arrangements
professional development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial managementbudget oversightdata cleaningKPI managementvendor managementcost projectionsregulatory compliancedocument preparationtrial feasibility assessmentstudy management

Soft Skills

leadershipinterpersonal skillseffective communicationstrategic direction implementationteam alignmentstakeholder interactionproblem-solvingadaptabilitytime managementpresentation skills