Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Contract Manager (Remote)

8-9 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Contract Manager (Remote)
Location:Cincinnati, Ohio
Department: Site Activation & Maintenance
Job ID: 10783

Job Summary:

Medpace is currently seeking a Senior Contract Manager to join its Clinical Operations team. This position can be office-based or remote (CRO experience is required for remote-based candidates). As part of the team, you'll work on pivotal tasks and projects that contribute to the company's success. This is a great opportunity for someone with expertise in clinical trial agreements (CTAs) and a desire to grow in the field.

Responsibilities:

  • End-to-End CTA Management: Oversee the entire process for clinical trial agreements (CTA) for global, multi-site clinical trials.
  • Strategy Development: Collaborate with the Sponsor and internal stakeholders to develop a study-specific CTA strategy.
  • Country-Specific Templates: Create country-specific CTA templates to ensure consistency and compliance.
  • Negotiations: Lead negotiations of CTAs and corresponding budgets directly with clinical sites.
  • Progress Reporting: Present progress to internal and external stakeholders, ensuring deliverables are met within agreed 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;
  • 3+ 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.
  • Skills:
    • Ability to effectively influence others.
    • Exceptionally strong communication skills.
    • Advanced knowledge of Microsoft Word, Excel, and PowerPoint.

Travel: Minimal

Medpace Overview:

Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Medpace aims to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With over 5,000 employees across 40+ countries, Medpace has vast local regulatory and therapeutic expertise in key therapeutic areas such as oncology, cardiology, metabolic disease, endocrinology, and more.

Why Medpace?

  • Purpose-Driven Work: Medpace’s work has positively impacted the lives of patients and families facing many diseases. The work continues to improve the lives of individuals worldwide.
  • Career Growth: Medpace offers structured career paths and professional growth opportunities.
  • Impactful Work Environment: Join a team that’s focused on making a difference in the field of clinical research.

Medpace Perks:

  • Flexible work environment.
  • Competitive compensation and benefits package.
  • Competitive PTO packages.
  • Structured career paths with professional growth opportunities.
  • Company-sponsored employee appreciation events.
  • Employee health and wellness initiatives.

This position is an excellent opportunity for someone with expertise in contract management and negotiation who wants to play a pivotal role in the success of global clinical trials. If you’re interested in making a difference and growing your career with a leading CRO, apply now