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Precision for Medicine

Global CRO for precision medicine trials

Site Contracts Manager

Contract ManagementConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A graduate, postgraduate, or four-year college degree is required.
  • Experience in a CRO or healthcare field is required.
  • At least five years of relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budget negotiations is required.
  • Experience leading interactions with Study Teams and Sponsors is required.
  • Strong organizational and written communication skills, with the ability to multitask and prioritize in a fast-paced environment, are required.
  • Ability to execute time-sensitive matters accurately and with attention to detail is required.
  • Ability to work and plan independently and as part of a team is required.
  • Professionalism, punctuality, reliability, service orientation, and positive customer and teammate interactions are required.
  • Sound business judgment and a proactive, independent work style are required.
  • Proficiency in Microsoft Office software programs and computer applications is required.
  • Ability to handle sensitive issues with discretion is required.
  • Ability to work independently and cooperatively with others in a virtual environment is required.
  • Ability to develop, maintain, and strengthen relationships with internal and external contacts who can provide information, assistance, and support is required.
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsibilities

  • Review, draft, negotiate, and track confidentiality agreements, master confidentiality agreements, clinical study agreements, amendments, master services agreements, site contracts, consulting agreements, vendor agreements, and other client contracts.
  • Work with the supervisor and internal and external stakeholders to resolve or 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 the maintenance and archiving of contract files and databases.
  • Assist in designing and implementing policies and procedures to support timely contract execution.
  • Identify opportunities to improve processes and take corrective action.
  • Perform other assigned tasks.

Desired Qualifications

  • A bachelor's degree in law, a scientific field, or business administration, or an equivalent degree, is preferred.
  • Knowledge of establishing Contracting Plans and guides for Clinical Trial Agreement and budget negotiations is preferred.
  • Successful relationship handling with study teams and/or Clinical Research Associates, Start-up Associates, or (S)BSCA to meet study timelines is preferred.

About the Company

Precision for Medicine

Global CRO for precision medicine trials

Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$225M
Headquarters
Bethesda, MD
Founded
2012

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