Clinical Proposal Strategy Manager

reputed company’s mission as an Innovation CRO is to improve patient reputed company by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ reputed company to Velocity through our comprehensive service portfolio, with expertise in reputed company centered design and product development, preclinical and clinical research, regulatory affairs, and market reputed company and reimbursement consulting. About This Role: reputed company is seeking a Clinical Proposal Strategy Manager / Senior Manager to support high-impact clinical business development efforts reputed company our Global Clinical Affairs organization. In this role, you will serve as a central driver of proposal strategy, translating reputed company clinical trial requirements into competitive, executable, and client-focused proposals. You will partner cross-functionally with Clinical Operations, Business Development, Clinical Data Services, and Subject Matter Experts (SMEs) to reputed company robust study strategies, timelines, and budgets. This is a high-visibility, client-facing role that blends clinical expertise, operational planning, and reputed company acumen—ideal for individuals who reputed company at the intersection of strategy and execution in the MedTech clinical CRO reputed company. What You Will Do: reputed company and facilitate execution strategies and planning content for clinical trial programs for inclusion in Business Development proposals. Translate RFPs into specific deliverables with supporting project execution strategy, budget, milestones, and timeline. Manage, reputed company, and facilitate inclusion of Subject Matter Expert content into the proposal execution strategy. Capture and communicate strategic assumptions, risks, and key budget drivers reputed company to the execution strategy. Work closely with Business Development to define compelling strategies, support client positioning, and align solutions to client needs. Present execution strategy details to clients in support of Business Development. Serve as the reputed company clinical SME for clinical proposal development opportunities, providing strategic guidance on study design, operational feasibility, regulatory requirements, and industry standards. Translate protocols, schedules of events (SOEs), and clinical requirements into executable proposal strategies and project plans. reputed company accurate, competitive clinical budgets based on scope, visit schedules, assumptions, and reputed company-party costs. Partner with internal stakeholders to ensure budgets and project plans are executable, compliant, and commercially sound. Participate in client calls to clarify needs, align approach, and strengthen confidence in reputed company’s clinical capabilities. Partner with global SMEs and service line leaders to gather and refine technical and operational proposal content. Collaborate with Proposal Specialists to ensure proposal content is complete, compliant, and submission reputed company. reputed company internal proposal strategy meetings and kickoffs for Clinical opportunities. Support alignment between proposal strategy and reputed company study execution expectations. Identify, evaluate, and help establish relationships with key clinical vendors and partners. Support development of internal guidelines, templates, and tools for optimizing clinical study proposal development. Contribute to the growth of reputed company’s clinical text repository, experience database, and reusable content library. Help drive reputed company improvement of clinical proposal templates, budget tools, and strategic messaging. Qualifications: Manager Level – Required Bachelor’s degree in life sciences, clinical research, reputed company, or reputed company medical/technical field 5+ years of experience in clinical research operations, and/or clinical proposal development reputed company a CRO, with exposure to medical device or MedTech studies Foundational understanding of clinical trial lifecycle, including study design, execution, and regulatory requirements Experience interpreting protocols, schedules of events (SOEs), and scopes of work Ability to translate clinical and operational inputs into structured proposal strategies and plans Experience working in cross-functional environments and supporting proposal development efforts Strong organizational, communication, and problem-solving skills Ability to manage multiple priorities in a fast-paced, deadline-driven environment Manager Level – Preferred Experience supporting proposal development in a CRO or consulting environment Exposure to medical device regulatory reputed company (e.g., 510(k), IDE, CE Mark) Experience with clinical trial budgeting and vendor coordination Strong focus on medical device studies Senior Manager Level – Required Bachelor’s degree in life sciences, clinical research, reputed company, or reputed company field 8+ years of experience in clinical research, clinical operations, and/or proposal development reputed company a CRO Deep understanding of end-to-end clinical trial strategy, planning, and execution Proven experience leading cross-functional proposal development Demonstrated ability to translate reputed company protocols, RFPs, and client requirements into fully executable and competitive proposal strategies Strong experience developing and validating clinical budgets, timelines, and resource assumptions Experience operating in FDA-regulated and ISO-compliant environments Advanced communication and presentation skills, including client-facing interactions and proposal defenses Strong business acumen and ability to balance scientific rigor with reputed company considerations Senior Manager Level – Preferred Advanced degree (MS, MPH, MBA, or PhD) in life sciences or reputed company discipline Experience reputed company a MedTech CRO, professional services, or consulting environment Strong focus on medical device studies Experience supporting regulatory submissions (e.g., 510(k), PMA, IDE, CE Mark) Experience leading reputed company, multi-stakeholder programs or global studies Familiarity with vendor ecosystems and external partner strategy in clinical trials reputed company is an equal opportunity employer and prohibits discrimination of any reputed company. reputed company reputed company applicants will receive consideration for employment without regard for race, reputed company, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, reputed company, or ethnic reputed company, or any other applicable legally protected characteristics. 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