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Site Contracts Manager

4 days, 2 hours ago
Serbia, Slovakia, Spain, Hungary, Poland, Romania
Full-time
Senior
Contract Manager
Project and Program Management
Apply Now
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012
View All Jobs 148

Description

  • Review, draft, negotiate, and track a variety of legal and clinical research agreements.
  • Manage master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts.
  • Work with supervisors and internal and external stakeholders to resolve or escalate contractual issues.
  • Ensure compliance with company policies, procedures, and contracting standards.
  • Update study team members on the status of contract negotiations and execution.
  • Establish, track, report, and manage site contract metrics.
  • Maintain contract files and databases, including contract archiving.
  • Assist in designing and implementing policies and procedures to support timely contract execution.
  • Identify process improvement opportunities and take corrective action.
  • Support other assigned tasks as needed.

Requirements

  • Graduate, postgraduate, or 4-year college degree.
  • At least 5 years of relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budget negotiations.
  • Experience in a CRO or healthcare field.
  • Experience leading interactions with study teams and sponsors.
  • Bachelor's degree in law, scientific fields, business administration, or an equivalent degree preferred.
  • Excellent organizational, written communication, and attention-to-detail skills preferred.
  • Knowledge of setting up contracting plans and guides for CTA and budget negotiations preferred.
  • Experience successfully working with study teams, CRAs, Start-up Associates, or (S)BSCAs to meet study timelines preferred.
  • Proficiency in MS Office software programs and computer applications.
  • Ability to work remotely from Poland, Slovakia, Spain, Serbia, Romania, or Hungary.

Benefits

  • Fully remote work from Poland, Slovakia, Spain, Serbia, Romania, or Hungary.
  • Opportunity to work on European clinical studies with a cross-functional team.
  • Equal Opportunity Employer status.
  • Reasonable accommodation support for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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