Entry Clinical Trials Proposal Writer
Sacred Heart University, Fairfield, Connecticut, us, 06828
and the job listing Expires on February 9, 2026
We are currently seeking a full-time, office-based 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
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
Qualifications
Bachelor’s degree in life science field required, Master’s degree in life science field preferred
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.
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We are currently seeking a full-time, office-based 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
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
Qualifications
Bachelor’s degree in life science field required, Master’s degree in life science field preferred
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.
#J-18808-Ljbffr