Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Precision Medicine Group

Site Contracts Manager

Precision Medicine Group

. Review, draft, negotiate, and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, amendment agreements, master services agreements, site contracts, consulting agreements, vendor agreements, and other client contracts .

Posted 9/15/2026full-timeRemote • SlovakiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in drafting, reviewing, and negotiating legal agreements within the healthcare sector, particularly Clinical Trial Agreements and Vendor Contracts. Strong organizational skills and attention to detail are essential for managing contract metrics and ensuring compliance with company policies.

Highest-signal resume keywords
Clinical Trial Agreement NegotiationVendor Contract ManagementMS Office ProficiencyOrganizational SkillsStakeholder Communication

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Contract DraftingContract NegotiationContract TrackingSite Budget NegotiationProcess Improvement
Soft Skills
Attention to DetailMultitaskingDiscretionTeam CollaborationWritten Communication
Tools & Technologies
Contract DatabasesContract Archiving Systems
Industry Keywords
CROHealthcareStudy TeamsSponsorsContracting Plans

About the role

Key responsibilities & impact
  • Review, draft, negotiate, and track legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, amendment agreements, master services agreements, site contracts, consulting agreements, vendor agreements, and other client contracts
  • Work with supervisors and internal/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
  • Support maintenance of contract files and databases, including contract archiving
  • Assist in designing and implementing policies and procedures for timely contract execution
  • Identify process improvements and take corrective action
  • Perform other assigned tasks

Requirements

What you’ll need
  • Graduate, postgraduate, or 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
  • Strong organizational and written communication skills
  • Ability to multitask and prioritize in a fast-paced environment
  • Ability to execute time-sensitive matters accurately and with attention to detail
  • Ability to work independently and in a team environment
  • Ability to handle sensitive issues with discretion
  • Ability to work cooperatively in a virtual environment
  • Preferred: Bachelor's degree in law, scientific fields, business administration, or equivalent degree
  • Preferred: Knowledge of setting up Contracting Plans and guides for CTA and budget negotiations
  • Preferred: Successful relationship handling with study teams and/or CRAs/Start-up Associates/(S)BSCA

Benefits

Comp & perks
  • Fully remote work arrangement
  • Regular full-time employment
  • Equal opportunity employment
  • Reasonable accommodation during the application process