Site Contracts Manager

2 hours, 13 minutes ago
Full-time
Senior
Project and Program Management
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

Description

  • Review, draft, negotiate, and track legal and clinical study agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements.
  • Review, draft, and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, and other client contracts.
  • Work with supervisors and internal and external stakeholders to resolve or escalate contractual issues.
  • 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.
  • Help design and implement policies and procedures that support timely contract execution.
  • Identify process improvement opportunities and take corrective action.
  • Support alignment of deliverables with defined study timelines.
  • Perform 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 environment.
  • Experience leading interactions with study teams and sponsors.
  • Bachelor’s degree in law, scientific fields, business administration, or an equivalent field preferred.
  • Excellent organizational, written communication, and attention-to-detail skills preferred.
  • Knowledge of contracting plans and guides for CTA and budget negotiations preferred.
  • Experience working successfully 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 independently, prioritize in a fast-paced environment, and handle sensitive issues with discretion.

Benefits

  • Fully remote work from Poland, Slovakia, Spain, Serbia, Romania, or Hungary.
  • Equal Opportunity Employer.
  • Reasonable accommodation available for applicants with disabilities during the application process.
  • Privacy policy and CA privacy notice provided for applicant data protection.

Interested in this position?

Apply directly on the company website

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