Job Description for Investigator Grants Manager-II (P2-3)
Preliminary Summary of Responsibilities:
• Responsible for working on opportunities (moderate to high complexity) for developing Investigator Grants Estimates (IGE).
• Develops detailed and accurate IGE at the RFP stage for clinical trials. May also assist on post-award Investigator Grants Estimates as applicable.
• Creates Investigator Grants Estimates utilizing Grant Plan tool based on available protocol and schedule of events.
• Ensures that IGEs are competitive yet realistic, reflecting the needs of the study while adhering to RFP/site requirements.
• Support on rebids for IGE revisions as study protocols are refined, keeping updated grant budgets aligned with any changes to scope, timeline, or requirements.
• Analyzes historical data from previous grants and studies to benchmark costs and ensure the accuracy and competitiveness of estimates.
• Ensures that all IGEs comply with sponsor specifications, RFP requirements, and any regulatory or institutional requirements.
• Performs quality control activities per the appropriate process/requirements.
• Work together with the Proposal team and SMEs to develop competitive budget strategies for Pre-sales business proposals, ensuring alignment with the Request for Proposal (RFP) requirements.
• Responsible for addressing any client questions or concerns related to IGEs.
• Drive the resolution of complex grant-related challenges, ensuring client-focused analysis and the effective management of study grants PRE & POST AWARD STAGE for successful project outcomes.
• Engage in specific initiatives aimed at enhancing processes, tools, systems, and the overall organization.
• Works across the organization in a matrix environment across multiple time-zones and locations to lead the process, align stakeholders, influence contributors, and complete deliverables.
• Identifies, evaluates, and resolves routine to moderately complex issues around client enquiry requirements and Fortrea capabilities; escalates high-risk or highly complex matters with recommended options.
• Ensures timely delivery of assigned deliverables.
• Provides guidance to less experienced team members on proposal process, tools, timelines, quality expectations, and content standards.
• Completes other appropriate duties, as assigned by the manager, which require similar skills in accordance with business needs and common sense.
• Leads or contributes to ways to improve the efficiency and quality of processes and the resulting deliverables, including content reuse, data accuracy, cycle time, and stakeholder experience.
Qualifications (Minimum Required):
• Bachelor’s degree required in related field or equivalent work experience.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience (Minimum Required):
• A minimum of 6 years of experience within the Clinical Research, Pharma and/or Biotech industry with at least 3 years of experience in grants and budget development.
• Strong financial acumen, with the ability to develop accurate and detailed Investigator Grants Estimates.
• Strong financial analysis, budgeting, and forecasting skills.
• Familiarity with clinical trial budgeting and cost structures (e.g., patient care costs, investigator fees, indirect rates).
• Proficiency in Microsoft Excel and Grants management software (e.g., Grants.gov, eRA Commons, or similar platforms).
• Attention to detail and the ability to manage multiple grant estimates and deadlines simultaneously and accuracy in managing financial data.
• Ability to work under tight deadlines and manage multiple budget submissions simultaneously.
• Familiarity with cost accounting standards and regulatory compliance
• Strong communication skills, both written and verbal, for explaining complex financial information clearly.
• Demonstrated ability to plan, multi-task and prioritize.
• Demonstrated teamwork, communication (written and verbal), and organizational skills.
• Proven ability to work independently.
• Ability to work to deadlines.
• Strong analytical skills.
• Ability to communicate appropriately and effectively with internal stakeholders, clients and Fortrea senior management.
• Positive attitude and sense of urgency.
• Possesses an ability and willingness to work across Business Units.
• Ability to work irregular and/or extended hours as needed to meet the client’s proposal deadline.
Learn more about our EEO & Accommodations request here.
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com
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