Medpace

Senior Contract Manager (Remote)

Medpace$90K — $130K *
US-AnywhereRemote in Cincinnati, OH
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant legal or business field
  • 8+ years of direct Clinical CRO experience
  • Site contract and budget negotiation experience
  • 4+ years of management or oversight experience
  • Ability to effectively influence others
  • Exceptional communication skills
  • Advanced knowledge of Microsoft Word, Excel, and PowerPoint

Responsibilities

  • Manage the clinical trial agreement (CTA) process for global, multi-site trials
  • Develop study-specific CTA strategy with Sponsor and stakeholders
  • Create country-specific CTA templates
  • Negotiate CTAs and budgets directly with sites
  • Present progress to stakeholders to ensure timely deliverables

Benefits

  • Flexible work environment (office or remote)
  • Opportunity for career growth and development
  • Work within a rapidly growing company
  • Be part of an impactful team in Clinical Operations
  • Engage in global, multi-site clinical trials
Full Job Description
Job Summary

We are growing rapidly, and currently seeking a full-time, office or remote-based Site Contract Manager to join our Clinical Operations team (CRO experience required for remote-based). This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

Responsibilities

  • End-to-end management of the clinical trial agreement (CTA) process for global, multi-site clinical trials
  • Develop the study-specific CTA strategy with the Sponsor and internal stakeholders
  • Develop country-specific CTA templates
  • Negotiate CTAs and the corresponding budget directly with sites
  • Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines.


Qualifications

  • Bachelor's degree (required) in relevant legal or business field;
  • 8+ years of direct Clinical CRO experience required;
  • Site contract and budget negotiation experience required;
  • 4+ years of management or oversight experience required;
  • Ability to effectively influence others;
  • Exceptionally strong communication skills; and
  • Advanced knowledge of Microsoft Word, Excel, and PowerPoint.


Travel: minimal

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

About Medpace

Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
Learn more about Medpace
Size
4,700 employees
Market Cap
$6.4 billion
Industry
Net Income
$145.3 million
Founded
1992
5 Year Trend
+22.1%
Revenue
$925.9 million
NASDAQ

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