Overview
Join our international Clinical Operations team as a Clinical Project Manager. As a Clinical Project Manager, you will be responsible for planning, organizing, and overseeing the execution of clinical trials, ensuring projects are completed on time, within budget, and in compliance with industry regulations. Position is in any EU country. Please provide CV in English language for assessment. Responsibilities: Manage and co-ordinate efforts of cross-functional teams, including 3rd party vendors, to support milestones achievement and compliance with company procedures and regulations Manage project budget including tracking, forecasting, identification of out-of-scope items and participation in the preparation of change orders Develop clinical project plans (project management, communication, monitoring and etc.) Lead clinical project team (internal resources and third parties/vendors) Ser
Full job description
Full Job Description
Join our international Clinical Operations team as a Clinical Project Manager.
As a Clinical Project Manager, you will be responsible for planning, organizing, and overseeing the execution of clinical trials, ensuring projects are completed on time, within budget, and in compliance with industry regulations.
Position is in any EU country.
Please provide CV in English language for assessment.
Responsibilities:
- Manage and co-ordinate efforts of cross-functional teams, including 3rd party vendors, to support milestones achievement and compliance with company procedures and regulations
- Manage project budget including tracking, forecasting, identification of out-of-scope items and participation in the preparation of change orders
- Develop clinical project plans (project management, communication, monitoring and etc.)
- Lead clinical project team (internal resources and third parties/vendors)
- Serve as the first point of contact for the sponsor providing regular updates on the project’s status
- Identify quality issues, implement appropriate corrective and preventive action plans
- Provide input and/or develop proposals for new projects
- Support business development by preparation and participation in bid defense meetings
Requirements
- Preferable Master or higher degree in Life Science field
- Fluent English language
- 5 years’ experience in Clinical Research field (Healthcare, Sponsor organization or CRO) with the responsibilities including organization and management of clinical projects
- Project management and study team management experience
- Experience in early phase clinical trials and oncology field is an advantage
- Reporting, time and risk management skills
- Familiarity with standard business and eClinical systems (CTMS, EDC, IXRS, eTMF and project planning tools)
Benefits
- International team and environment
- Performance based annual bonus
- Remote Work, workation & Flexibility
- Health & Wellbeing – wellness initiatives
- Professional growth and development in the Life science industry
- Team Culture – Team buildings, global meetings, and B Active events.
- Comprehensive Insurance - Personal accident, business trip coverage, and additional health insurance.
Qualifications And Requirements
Mid-Senior level
Requirements & qualifications
Mid-Senior level
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Verification notes
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