Site Contracts Manager

2 hours, 6 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 a variety of legal and clinical research 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 Clinical Operations study teams and other internal and external stakeholders to resolve or escalate contractual issues.
  • Ensure adherence to company policies, procedures, and contracting standards.
  • Provide regular updates to 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 policies and procedures that support timely contract execution.
  • Identify process improvement opportunities and take corrective action.
  • Work independently and collaboratively in a virtual environment to support study timelines and deliverables.
  • Perform other assigned tasks as needed.

Requirements

  • Graduate, postgraduate, or 4-year college degree.
  • At least 5 years of relevant experience in 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 degree preferred.
  • Excellent organizational, written communication, and interpersonal skills.
  • Strong attention to detail and ability to multitask and prioritize in a fast-paced environment.
  • Proficiency in MS Office software programs and computer applications.
  • Ability to handle sensitive issues with discretion.
  • Experience working effectively with CRAs, Start-up Associates, and/or (S)BSCAs to meet study timelines is preferred.

Benefits

  • Fully remote work from Poland, Slovakia, Spain, Serbia, Romania, or Hungary.
  • Equal Opportunity Employer status.
  • Accommodation support for applicants with disabilities during the application process.
  • Privacy protections for applicant data in accordance with the company Privacy Policy and CA Privacy Notice.

Interested in this position?

Apply directly on the company website

Apply Now

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