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Contract Administrator III — Medical Device (Remote — United States) Contract with Possible Extension

Key Facts

Remote From: 
Fixed term
Mid-level (2-5 years)
English

Other Skills

  • Microsoft Excel
  • Microsoft PowerPoint
  • Microsoft Word
  • Decision Making
  • Professionalism
  • Ability To Meet Deadlines
  • Communication
  • Time Management
  • Detail Oriented
  • Prioritization
  • Social Skills
  • Problem Solving

Roles & Responsibilities

  • 5+ years of professional experience with a bachelor's degree; OR a high school diploma/GED or associate degree with 7+ years in a related role, preferably within the legal department of a medical device or pharmaceutical company.
  • Thorough understanding of clinical contracting terms and conditions; clinical contracting experience (non-negotiable)
  • Ability to read and understand contract terms, redline agreements, and negotiate with a practical, business-minded approach
  • Strong computer skills (including Microsoft Office and Adobe software) with advanced proficiency in Word, Excel, and PowerPoint, and good communication skills

Requirements:

  • Prepare clinical study agreements and related documents using approved templates for sponsored studies at clinical sites worldwide.
  • Independently review revisions proposed by clinical sites and revise based on practices and procedures.
  • Raise contract issues as appropriate and liaise between Legal, Risk Management, clinical teams and other internal stakeholders to resolve issues.
  • Manage a high-volume workload in a fast-paced environment; ensure agreements and related documents are executed properly and uploaded to the contract management system, and organize/maintain the contract management system and Microsoft Teams folders.

Job description

This is a remote position.

Our F500 Medical Device client has an exciting opportunity for a Contract Administrator III

 

Job Summary:

This legal department position will support clinical studies across a global organization through preparation, review and negotiation of a high volume of clinical study agreements and related agreements/documents by working with global internal business partners and external vendors to facilitate the contracting process.

 

Responsibilities:

• Using approved templates, prepare clinical study agreements and related agreements and documents (e.g., hospital use agreements, device purchase agreements) for sponsored studies performed at clinical sites located around the globe

• Independently review revisions proposed by clinical sites and revise based upon practices and procedures

• Raise contract issues as appropriate and liaise between Legal, Risk Management, clinical teams and other internal stakeholders to resolve such issues

• Ability to manage and prioritize a high-volume workload in a fast-paced working environment

• Interface with Clinical, Contract Research Organizations and Global Clinical Operations contract support teams

• Ensure agreements and other related documents are executed properly and uploaded to the contract management system

• Organize and maintain contract management system and Microsoft Teams folders

 

Required Qualifications:

• 5+ years of professional experience with bachelor’s degree; OR High School Diploma or GED or associate degree with 7+ years in a related role, preferably within the legal department of a medical device or pharmaceutical company.

• Thorough understanding of clinical contracting terms and conditions

**Clinical contracting experience (non-negotiable)

• Able to read and understand contract terms, redline agreements, and make decisions with a practical, business-minded approach to contract negotiation

• Strong computer skills (including Microsoft Office and Adobe software) with advanced skills with Word, Excel, and PowerPoint.

**good communication skills

 

Preferred Qualifications:

* Med device experience a plus

• Capable of coordinating and prioritizing multiple tasks/projects while maintaining accuracy and meeting deadlines.

• Capacity to interact professionally with internal stakeholders across the globe.

 

Other Details:

Schedule: 08:00:AM - 04:30:PM

Work Setup: Remote (Must be based in the U.S.)

Contract Length: 6 Months (2/16/2026 - 8/15/2026)



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