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Medpace · 2 days ago

Entry Clinical Trials Proposal Writer

Cincinnati, OH

Full-time

Onsite

New Grad, Entry Level

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. They are seeking a full-time Proposal Writer to prepare proposals for new business in the pharmaceutical industry, collaborating with operations and business development teams to develop strategic content.

BiotechnologyPharmaceutical

Responsibilities

May 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 timeline

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 informationReview

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