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Recursion

👥 11-50Cloud Data ServicesMortgageFinanceAnalytics💼 Private Company
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Recursion is a technology company focused on advanced solutions in artificial intelligence and high-performance computing, emphasizing innovation in storage engineering.

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Jobs at this company:

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🔥 HiBob (HRIS) Implementation Contractor
Posted 9 days ago

📍 United States

🧭 Contract

  • Proven experience implementing HiBob or similar HRIS platforms.
  • Strong knowledge of HR processes, data management, and system integrations.
  • Experience with HR data migration and ensuring data integrity.
  • Ability to configure and customize HRIS platforms based on business needs.
  • Strong project management skills with the ability to meet deadlines.
  • Excellent problem-solving, communication, and stakeholder management skills.
  • Understanding of compliance requirements related to HR data and systems.
  • Previous experience in a contractor or consultant role preferred.
  • Partner with other leads on the implementation of HiBob HRIS, including configuration, data migration, and system optimization.
  • Collaborate with People and IT teams to define system requirements, workflows, and reporting needs.
  • Manage data migration from legacy HR systems, ensuring accuracy and compliance.
  • Customize HiBob modules, including onboarding, performance management, payroll, time tracking, and benefits.
  • Provide training and support to People Teams and other key stakeholders to ensure system adoption.
  • Develop documentation, best practices, and user guides for HiBob usage.
  • Troubleshoot technical issues and coordinate with HiBob support when necessary.
  • Ensure compliance with data security and privacy regulations throughout implementation.
  • Monitor system performance and suggest enhancements for improved efficiency.

Project ManagementHR ManagementComplianceStakeholder management

Posted 9 days ago
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🔥 Associate Director/Director of Statistical Programming
Posted about 1 month ago

📍 United States, Canada, United Kingdom

🧭 Full-Time

💸 162000.0 - 281000.0 USD per year

🔍 Biotechnology

  • BS/MS degree in life science, computer science, statistics, mathematics, or equivalent relevant degree.
  • 8+ years of statistics and programming experience with advanced knowledge in pharmaceutical, biotechnology industries, and 5+ years of serving as Lead Statistical Programmer across multiple therapeutic areas.
  • Demonstrated proficiency in SAS, R, and R-Shiny and mastery of complex graphing techniques to derive analysis datasets, produce tables, figures and listings, and conduct exploratory analyses.
  • Expert knowledge of data standards including CDISC, SDTM, and ADaM, and relevant regulatory guidelines.
  • Experience with regulatory submissions in the US, Europe, and other regions.
  • Excellent interpersonal and communications skills including ability of conflict management and resolution.
  • Lead statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, analysis datasets.
  • Oversee external functional service providers to ensure timely and high-quality programming deliverables
  • Develop and maintain standards, guidance, applications, and processes for Statistical Programming operations in adherence with ICH and regulatory requirements.
  • Drive the adoption of innovative programming technologies and workflows to enhance the efficiency of clinical data review, cleaning, reconciliation, and integration. Additionally, develop analytics tools that enable effective data monitoring and knowledge discovery of clinical data.

LeadershipProject ManagementSQLData AnalysisPeople ManagementCross-functional Team LeadershipCommunication SkillsAnalytical SkillsMicrosoft ExcelProblem SolvingAgile methodologiesMentoringAttention to detailOrganizational skillsWritten communicationInterpersonal skillsExcellent communication skillsAdaptabilityCritical thinkingTeamworkFluency in EnglishStrong communication skillsData visualizationStrategic thinkingProcess improvementResearch skillsTechnical supportFinancial analysisData modelingBudget management

Posted about 1 month ago
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🔥 Senior Director of Clinical Development
Posted 3 months ago

📍 United States

💸 250000.0 - 305000.0 USD per year

🔍 Biotechnology

  • Medical Degree and MD/PhD preferred.
  • 5+ years of experience in developing, executing and analyzing clinical trials (ideally Phase 1/2).
  • Deep knowledge and understanding of oncology and genetic diseases; precision oncology drug development paradigms.
  • Clinical pharmacology with technical and regulatory approaches.
  • Strong networks and connections to external experts and key opinion leaders in oncology.
  • Ability to form effective collaborations with external scientific community, academia and CROs.
  • Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders.
  • Highly motivated, decisive, and results-oriented individual who is proactive, resourceful, and efficient.
  • Oversee the development of first-in-class/first-in-disease molecules in precision oncology.
  • Generate and continually refine the integrated clinical development strategy for the oncology medicine portfolio from IND to POC.
  • Contribute to regulatory submissions and participate in regulatory agency meetings.
  • Utilize strong therapeutic area expertise to enhance innovation and efficiency in clinical trial design and execution.
  • Deliver medical, disease-specific, and development perspective into specific research programs or broader research initiatives.
  • Provide scientific and medical expertise for business development assessments and due diligences.

CollaborationStakeholder management

Posted 3 months ago
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🔥 Director of Clinical Development
Posted 3 months ago

📍 Salt Lake City, remote

💸 234000.0 - 286000.0 USD per year

🔍 Biotechnology

  • Medical Degree and MD/PhD preferred.
  • 3+ years of experience in developing, executing and analyzing clinical trials (ideally Phase 1/2) and preferably within a biotech or pharmaceutical company.
  • Deep knowledge and understanding of oncology and genetic diseases; precision oncology drug development paradigms, clinical pharmacology with technical and regulatory approaches.
  • Strong networks and connections to external experts and key opinion leaders in oncology.
  • Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders.
  • Highly motivated, decisive, and results-oriented individual who is proactive, resourceful, and efficient.
  • Oversee the development of first-in-class/first-in-disease molecules in precision oncology.
  • Generate and continually refine the integrated clinical development strategy for Recursion’s oncology medicine portfolio from IND to POC.
  • Contribute to regulatory submissions and participate in regulatory agency meetings.
  • Utilize strong therapeutic area expertise to enhance innovation and efficiency in clinical trial design and execution.
  • Deliver medical, disease-specific, and development perspective into specific research programs or broader research initiatives.
  • Provide scientific and medical expertise for business development assessments and due diligences.

Stakeholder management

Posted 3 months ago
Apply