Experienced Clinical Trials Proposal Writer Job Locations United States-OH-Cincinnati Category Feasibility & Proposals Job Summary We are currently seeking a full-time, office-based Experienced Proposal Writer to join our Proposal and Feasibility team. This position will work closely with the operations and business development teams to prepare proposals for new business in the pharmaceutical industry with the opportunity to develop strategical content at the intersection of science, operations and financewhile developing your career. If you want an exciting career where using your previous expertise and while developing and growing your career even further, this is the opportunity for you! 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 Qualifications Bachelor's degree in life science field required, Master's degree in life science field preferred 2-3 years of CRO experince or Proposal Writing experience within industry Strong initiative to learn Strong written and oral communication skills Project management skills and the ability to prioritize multiple projects and tasks Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks Cincinnati Campus Overview Hybrid work-from-home options (dependent upon position and level) Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Flexible work schedule Company-sponsored employee appreciation