P

Precision AQ

Data-driven drug access and launches

Site Contracts Manager

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

About the Job

Requirements

  • A graduate, postgraduate, or 4-year college degree is required.
  • Experience in a contract research organization or healthcare field is required.
  • At least 5 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 and 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 independently and plan work as well as collaborate in a team environment is required.
  • Proficiency in Microsoft Office software programs and computer applications is required.
  • Ability to handle sensitive issues with discretion is required.
  • Ability to develop, maintain, and strengthen relationships with internal and external stakeholders is required.
  • Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsibilities

  • Review, draft, negotiate, and track 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 the supervisor and internal and external stakeholders to resolve or escalate contractual issues.
  • Ensure adherence to 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.
  • 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 tasks as assigned.

Desired Qualifications

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

About the Company

Precision AQ

Data-driven drug access and launches

Precision AQ helps pharmaceutical companies get FDA-approved medicines to patients by using data, evidence, and market insights to shape access and launches. Its services combine medical science, commercial strategy, and technology development to create new pathways for drug availability and timely delivery. The company partners with drug makers to plan launches and expansion, using analytical and creative approaches to make medicines reachable and effective in real-world settings. Unlike firms that focus only on science or marketing, Precision AQ blends data-driven insights with strategic execution across development and commercialization to accelerate patient access. The goal is to raise standards in healthcare accessibility and impact by getting the right medicines to the right patients faster.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
New York City, New York
Founded
Not listed

Recently Posted Jobs

Explore more opportunities at Precision AQ

See more jobs