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Medpace, Inc.

Director of Proposal Writing

City of London
$0/yr
Posted 5 months ago
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Director of Proposals

Medpace is currently seeking an office-based Director of Proposals to join our Clinical Operations team at our London office. 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 the latest industry tactics and strategies regarding proposal development
  • 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
  • Demonstrated ability to effectively interact face-to-face with Sponsors and represent the company in outside settings

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Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

  • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

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Collaborative Culture

  • Contribute to an interactive team environment that empowers decision-making, creative thinking, and continuous learning through open communication and mutual trust
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

  • Office-based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry-renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

  • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office-based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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Skills

Leadership
Writing
Problem Solving
Project Management
Clinical Trial Management
Time Management
Planning
Organizational Skills
Communication Skills
Decision-Making
Drug Development
GCP Guidelines
Proposal Development
Client Interaction
Quality Control
Strategic Thinking

Location

City of London, England, United Kingdom

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