Manager jobs in Poland
Explore 58 matching jobs.
Site Contracts Manager
Precision For Medicine
Posted: 10/21/2026Site Contracts Manager
Precision For Medicine
Posted: 10/21/2026Site Contracts Manager
Precision For Medicine
Posted: 10/21/2026Site Contracts Manager
Precision For Medicine
Posted: 10/21/2026Site Contracts Manager
Precision Medicine Group
Posted: 10/21/2026Site Contracts Manager
Precision Medicine Group
Posted: 10/21/2026Site Contracts Manager
Precision Medicine Group
Posted: 10/21/2026Fleet Manager
Helprise
Posted: 10/20/2026Global Study Manager
ICON plc
Posted: 10/19/2026Platform Manager
LITE TECH, INC.
Posted: 10/19/2026Global OE Manager
Umicore
Posted: 10/19/2026District Manager
beeline Group (Fashion Accessories)
Posted: 10/14/2026Global Study Manager – Single Sponsor, EMEA
IQVIA
Posted: 10/14/2026Regional Facilities Manager
Jones Lang LaSalle Americas, Inc.
Posted: 10/14/2026Global Sector Manager
Dentons
Posted: 10/14/2026Outsourcing Manager
Helprise
Posted: 10/13/2026Manager, FSA
ICON plc
Posted: 10/9/2026Community Outreach Manager – Temporary Parental Leave Coverage
World Central Kitchen
Posted: 10/9/2026Senior Manager, MED Oncology RWE/Epi Scientist
Pfizer
Posted: 10/8/2026Senior Manager, MED Oncology RWE/Epi Scientist
Pfizer
Posted: 10/8/2026
Site Contracts Manager
Precision For MedicineCore Competencies
Role fitUse this summary to align your resume positioning with the role.
Demonstrates expertise in drafting, reviewing, and negotiating clinical trial agreements and vendor contracts while ensuring compliance with company policies and procedures. Proven ability to collaborate with stakeholders and manage contract metrics effectively.
About the role
Key responsibilities & impact- Review, draft, negotiate and track confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments
- Review, draft and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements and other client contracts
- Collaborate with supervisors and internal and external stakeholders to resolve or escalate contractual issues
- Ensure adherence to company policies, procedures and contracting standards
- Update study team members on contract negotiation and execution status
- Establish, track, report and manage site contract metrics
- Maintain contract files and databases, including contract archiving
- Assist in designing and implementing procedures for timely contract execution
- Identify process improvement opportunities and take corrective action
- Work with Clinical Operations study teams to align deliverables with study timelines
- Perform other assigned tasks
Requirements
What you’ll need- Graduate, postgraduate, 4-year college degree
- Experience in a CRO/healthcare field
- At least 5 years of relevant experience drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations
- Experience leading interactions with Study Teams and Sponsors
- Proficiency in MS Office software programs and computer applications
- Ability to work independently and in a team environment
- Candidates must be legally authorized to work in the country of employment without employer sponsorship
- Bachelor's degree in law, scientific fields, business administration or equivalent degree preferred
Benefits
Comp & perks- Fully remote work arrangement
- Regular full-time employment
- Equal opportunity employment
- Reasonable accommodation for applicants with disabilities
ATS Keywords
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