Medpace

Director of Feasibility & Proposals

Medpace$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree minimum, advanced degree preferred.
  • 5+ years of project management/clinical trial management experience; CRO experience preferred.
  • Strong leadership, writing, and problem-solving skills.
  • Superior time management, planning, and organizational skills.
  • Advanced knowledge of drug development and clinical trial procedures, including GCP guidelines.
  • Effective communicator with experience in client interactions.

Responsibilities

  • Mentor and lead proposal writers in creating strategic proposals and managing quality control.
  • Review RFPs for capacity issues and negotiate deadlines with executives.
  • Participate in pre-RFP client meetings to align on expectations.
  • Collaborate with business development and medical teams to design compelling proposals.
  • Contribute operational strategies to proposals for execution clarity.
  • Revise proposal content for strategic alignment and clarity.
  • Engage in client discussions post-delivery of proposals.
  • Lead improvements in proposal development processes.

Benefits

  • Flexible work environment.
  • Competitive PTO starting at 20+ days.
  • Company-sponsored employee appreciation events.
  • Employee health and wellness initiatives.
  • Structured career paths with growth opportunities.
  • Discounted tuition for UC online programs.
  • Modern, ecofriendly campus with an on-site fitness center.
Full Job Description
Job Summary

Medpace is currently seeking an office or home based Director of Proposals to join our Clinical Operations team at our HQ in Cincinnati, OH. The Director will collaborate closely with our medical experts and senior functional managers to create the operational strategy for new business development opportunities. This will include direct management of the proposal team.

Responsibilities

  • Mentor/Lead Proposal Writers in the preparation of compelling, strategic proposals, rebids, and exhibits, including rigorous quality control and timeline adherence;
  • Review RFPs, identify any capacity issues, and negotiate deadlines with Business Development Executives, as needed;
  • Participate in pre-RFP client meetings;
  • Partner with Business Development, Medical and Operational personnel to design effective proposals;
  • Contribute strategic operational content to proposals;
  • Review and revise proposal content as needed to ensure a clear, compelling strategy to execute the trial is articulated;
  • Participate in client discussions and requests for information following delivery of proposal;
  • Lead the enhancement of proposal development tools and processes;
  • Stay abreast of latest industry tactics and strategies regarding proposal development; and
  • May be responsible for other projects and responsibilities as assigned.


Qualifications

  • Bachelor's degree minimum, advanced degree preferred.
  • Highly-proficient employee with strong leadership, writing and problem solving skills;
  • 5+ years of project management/clinical trial management experience in clinical research; CRO experience preferred;
  • Must possess superior time management, planning and organizational skills, written and verbal communication skills, and quality decision-making skills;
  • Advanced knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines; and
  • Demonstrated ability to effectively interact face-to-face with Sponsors and represent company in outside settings.


Cincinnati Perks
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs


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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