Love writing. Thrive on deadlines. Interested in clinical research?
We’re hiring an RFI Associate to support global business development opportunities in a fast‑paced CRO environment. You’ll help manage RFIs end‑to‑end — reviewing requirements, pulling inputs from SMEs, drafting and QC’ing content, and keeping everything on track to deadline.
You’ll work closely with experienced Proposal Managers, gain exposure to higher‑complexity opportunities, join strategic calls, and build strong knowledge of clinical, regulatory, and sponsor expectations.
Summary of Responsibilities:
Responsible for managing RFI opportunities of low to medium complexity, with support.
Assists Proposal Managers with responses to Requests for Information [RFIs] (i.e., collating data, following up with other departments, meeting minutes, etc.).
Shadow and/or assist more senior colleagues on opportunities of medium to high complexity.
Review and analyze RFI documents to gain understanding of client requirements and to assist in identifying missing information for RFI response preparation. Collates follow-up questions for additional information as requested.
Attend strategic and operational calls related to the opportunity.
Works across the organization in matrix environment across multiple time-zones and locations to facilitate the process and complete deliverables.
Drafts standard documents in accordance with Sponsor requirements and expectations under the pressure of changing timelines.
Administratively supports facilitating internal and external opportunity management negotiations as needed.
Ensures timely delivery of assigned deliverables.
Escalates issues/challenges to Manager for support on resolution.
Performs timely and accurate data entry into departmental and/or corporate databases/systems as directed.
Seeks appropriate knowledge of the technical and regulatory environments.
Contributes to assigned process improvement initiatives and supports implementation.
Perform quality control activities per the appropriate process/requirements.
Expected to contribute to content library by submitting new content or updates to existing content, using the official content submission process. May be requested to handle the content submission for more senior colleagues.
Completes other appropriate duties, as assigned by the manager, which require similar skills in accordance with business needs and common sense.
Qualifications (Minimum Required):
Bachelor’s degree required in related field or equivalent work experience.
Experience (Minimum Required):
Minimum 2 years of experience in text development (RFI or RFP acceptable), or an equivalent combination of education and CRO/pharma/other related experience to successfully perform the essential job duties.
Excellent customer service skills, attention to detail and ability to be persistent while maintaining tact.
Demonstrated computer skills – requires excellent MS Office experience (specifically Excel, Word, Outlook).
Knowledge of RFI and/or proposal management software applications (e.g., Salesforce.com, Responsive, Sharepoint, other RFI/Proposal Automation applications) is a plus.
Demonstrated text editing and writing skills (based on business unit and/or team expectations).
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.
Positive attitude and sense of urgency.
Ability to work irregular and/or extended hours as needed to meet the client’s proposal deadline.
#LI-REMOTE
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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