This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Condor Software is seeking a seasoned FP&A professional to join our team as a Clinical Finance Engagement Manager. This role leads customer implementations end-to-end while serving as an FP&A subject-matter expert for biopharma R&D, combining hands-on delivery with deep planning and forecasting expertise across client and internal engagements. - Own implementations end-to-end for assigned clients, from discovery through go-live and early adoption. - Serve as an internal FP&A expert at Condor, acting as a thought partner and escalation point for complex forecasting, planning, and modeling topics. - Work directly with FP&A leaders, R&D finance teams, and senior stakeholders to ensure Condor is configured to support decision-ready planning and forecasting use cases. - Help customers move from spreadsheet-driven planning to system-based, decision-ready FP&A workflows. Key Responsibilities - Own end-to-end delivery of client implementations, serving as the primary owner from discovery through go-live and early adoption. - Lead structured discovery focused on FP&A requirements, including trial-level and portfolio-level planning assumptions, cost drivers, and governance models. - Configure Condor to support budgeting, AI-guided forecasting, dynamic scenario modeling, and portfolio-level planning use cases. - Act as a trusted advisor to client FP&A, finance, and clinical operations stakeholders, guiding planning and forecasting decisions throughout the implementation lifecycle. - Serve as an FP&A subject-matter expert across Condor engagement teams, providing guidance and escalation support for complex forecasting, portfolio analysis, and modeling challenges. - Validate configurations through walkthroughs, testing, and targeted client training, ensuring outputs are accurate, usable, and decision-ready. - Partner with Product, Engineering, and other Condor teams to improve FP&A-related capabilities, templates, and best practices based on real-world client use cases. - Provide continuity immediately post go-live, supporting early adoption, stabilization, and handoff into steady-state usage. Qualifications - Bachelor’s degree in Finance, Accounting, Economics, or a related field. - 8 or more years of progressive FP&A and R&D finance experience within biopharma or in advisory roles supporting biopharma organizations. - Direct, hands-on experience building and owning clinical trial forecasts, portfolio plans, and scenario models. - Deep understanding of clinical trial cost structures, enrollment-driven forecasting, and portfolio prioritization. - Proven experience in a client-facing role such as software implementation, professional services, consulting, or customer success. - Ability to engage senior FP&A and finance leaders with credibility and confidence. - Strong written and verbal communication skills, including the ability to explain complex models and assumptions clearly. - Advanced Excel skills, including complex financial modeling and scenario analysis. - Strong analytical and problem-solving skills, with comfort navigating ambiguity and incomplete information. - Ability to manage multiple engagements while maintaining high standards of quality and responsiveness. - Experience establishing FP&A standards, processes, or best practices across teams or portfolios. Preferred - MBA or advanced degree in Finance, Accounting, or Business Administration. - Experience implementing or owning FP&A, planning, or analytics platforms in an R&D or clinical context. - Experience using AI-powered tools to improve forecasting efficiency, modeling quality, or insight generation. - Prior experience in a fast-growing or startup environment. Personal Attributes - Client-first mindset with a strong sense of ownership and accountability. - High standards for analytical rigor, accuracy, and professionalism. - Comfortable operating as both an individual contributor and an internal expert within a growing team. - Self-directed, adaptable, and effective in a dynamic, high-expectation environment. Benefits - Competitive compensation and meaningful equity participation. - Comprehensive employee benefits, including 100% company-paid health, dental, vision, and life insurance. - 401(k) plan with a 3% company match that vests immediately. - Unlimited PTO. Company Description Condor exists to change the financial infrastructure behind clinical operations and finance, connecting clinical operations, vendor activity, and financial signals into a single, real-time intelligence layer.

• Assist with CRF review and testing: Support review of case report forms for completeness, clarity, and alignment with the protocol; participate in UAT testing in EDC systems. • Data cleaning support: Run predefined data checks, identify missing or inconsistent data, and help draft or track data queries under supervision. • Data reconciliation activities: Assist with reconciling clinical data against external sources (e.g., device logs, imaging data, or safety data listings). • Database documentation maintenance : Help maintain data management documentation such as data management plans (DMPs), data dictionaries, and data validation specifications. • Clinical systems support: Assist with user access tracking, training documentation, and basic system support for EDC or CTMS platforms. • Data tracking and reporting: Create simple metrics or dashboards (e.g., query rates, data entry timeliness) to support study oversight. • Process improvement and SOP support: Participate in reviewing SOPs or work instructions and help identify opportunities to improve data management workflows.

• Assist Clinical Program Manager with set-up of regional CRO and other vendors as required, including liaising with Global CRO to ensure site training and timely initiation. • Day-to-day contact with counterpart at CRO and/or trial site; daily review and identification of potential issues or problems with the sites and communicates/escalates to Clinical Program Manager. • Proactively identifies potential operational challenges and in collaboration with senior team members provides solutions to ensure study execution remains on track. • Under supervision may serve as the key operational contact for Akero studies aiding in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs. • Performs accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure correct study procedures according to SOPs and protocol procedures, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required. • Under supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports. May assist in compilation of investigator brochures under close supervision. • Review of trip reports generated by CRO CRAs. • Maintains study timelines. • Coordinates review of data listings and preparation of interim/final clinical study reports, including resolving data discrepancies. • Provides regular study updates to the appropriate internal stakeholders. • Maintains internal Clinical Operations databases and document repositories. • Performs administrative duties in a timely manner as assigned.

Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges. At Rho, you’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to take risks, innovate, and develop over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve. We are currently hiring a Senior Clinical Research Associate (with Psychiatry (preferably MDD) experience to join our team! As our next Senior CRA, you will play an integral to driving project success. You’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Rho Standard Operating Procedures. For this role, you’ll need proven monitoring skills in order to conduct site visits to assess site adherence to protocol and regulatory requirements as well as manage required documentation. You will also be responsible for ensuring the data remains audit ready and able to pass an audit by Rho, the Sponsor, or a regulatory agency.   This position is a remote role to be located within a 1-hour commute of a US metropolitan airport with the commitment to conduct 8-10 site visits days per month (up to 80% travel). Our Clinical Monitoring team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! What you'll be doing: - Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV) - Participate in the site selection process with oversight from the Clinical Team Lead role - Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved - Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials - Provide mentoring, training, and co-monitoring of junior clinical team members - Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements - Attend and present at meetings and conferences, including Investigator Meetings - Participate in the RFP process, including business development meetings - Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials - Perform both onsite & remote monitoring and study closure activities across multiple protocols