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Precision for Medicine seeks a Site Contracts Manager to join the European team, working fully remotely from Poland, Slovakia, Serbia, Romania, or Hungary.
You will review, draft, negotiate, and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements. You will work closely with the Clinical Operations study team and play a key role in ensuring deliverables align with defined study timelines.
Key responsibilities include:
- Review, draft, and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts
- Work with your supervisor and internal/external stakeholders to resolve and escalate contractual issues
- Ensure adherence to company policies, procedures, and contracting standards
- Update relevant study team members on contract negotiation and execution status
- Establish, track, report, and manage site contract metrics
- Support maintenance of contract files and databases, including archiving
- Assist in designing and implementing policies and procedures for timely contract execution
- Identify process improvement opportunities and take corrective action
- Perform other assigned tasks
You will need strong organizational and written communication skills, the ability to multitask and prioritize in a fast-paced environment, and the capacity to execute time-sensitive matters while maintaining accuracy and attention to detail. You should be self-motivated, able to work independently and collaboratively, demonstrate professionalism and sound business judgment, and handle sensitive issues with discretion. Proficiency in MS Office and computer applications is required, along with the ability to work effectively in a virtual environment and develop strong relationships with colleagues and external partners.
REQUIREMENTS:
Minimum Required:
- Bachelor's degree or higher (4-year college degree minimum)
- Experience in a CRO (Contract Research Organization) or healthcare field
- At least 5 years of relevant experience in drafting, reviewing, and negotiating site Clinical Trial Agreements, Vendor Contracts, and Site Budget negotiations
- Demonstrated experience leading interactions with Study Teams and Sponsors
Preferred:
- Bachelor's degree in law, scientific fields, business administration, or equivalent
- Knowledgeable in setting up Contracting Plans and Guides for CTA & Budget negotiations
- Successful track record managing relationships with study teams, CRAs, Start-up Associates, or BSCAs to meet study timelines
- Candidates must be legally authorized to work in the country of employment without employer sponsorship
