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Medpace · 2 days ago

Experienced Clinical Trials Proposal Writer

Cincinnati, OH

Full-time

Onsite

Entry, Mid Level

2+ years exp

Medpace is a full-service clinical contract research organization (CRO) focused on accelerating the global development of medical therapeutics. The Experienced Proposal Writer will collaborate with operations and business development teams to prepare proposals for new business, ensuring high-quality contributions and alignment with client requirements.

BiotechnologyPharmaceutical

Responsibilities

Lead proposal planning meetings to:

Identify issues and client requirements

Recommend proposal and overall study strategies, based on experience

Encourage multi-disciplinary discussions among subject matter experts to facilitate full and high-quality contributions to the text

Establish timelines and deliverables and hold internal stakeholders accountable to those plans and timelines

Extract relevant content from Subject-Matter Experts and consolidate this expertise into a meaningful proposal narrative

Include relevant data visualization materials into documents

Review and analyze Request for Proposal (RFP) and Request for Information (RFI) documents to gain understanding of client requirements and assist in identifying missing information

Identify information to be addressed in proposal text

Collate follow-up questions for additional information as requested

Draft standard documents in accordance with agreed strategy and Sponsor requirements within often expedited timelines

Contribute to assigned process improvement initiatives and support implementation

Define action plans and timelines; manage and determine modifications needed to ensure proposal alignment with client requirements and business strategies

Perform quality control/peer review and participate in the finalization of documents and distribution to the customer and internal departments