Director, Data Systems And Clinical Programming

Alumis Inc

South San Francisco, CA, USA
Base: $200,000 - $225,000 usd annually; bonus/equi...
Onsite tuesday-thursday, with remote work allowed 1-2 times per quarter.
Data systems and clinical programming
Ai-related initiatives for dm
Edc platform validation
Alumis Inc. is seeking a Director of Data Systems and Clinical Programming to lead their Clinical Programming function within Data Management, focusing on optimizing data flow, enhancing data quality, and driving technology solutions. The ideal candidate will have extensive experience in clinical trials, data management, and a strong proficiency with key technologies and regulatory standards. This role emphasizes leadership, collaboration, and innovation in transforming patient outcomes in autoimmune disease treatments

Job Summary

  • The Director, Data Systems (DS) and Clinical Programming (CP) will be responsible for leading and managing the Clinical Programming function within Data Management (DM).
  • Drive the implementation of various technology solutions to augment existing DM processes, optimize efficiency and enhance overall data quality assurance.
  • Mentor and develop team members, fostering a culture of continuous learning and growth within the team.

Matching Summary

Match Score: 85

Alumis Inc. is seeking a Director of Data Systems and Clinical Programming to lead their Clinical Programming function within Data Management, focusing on optimizing data flow, enhancing data quality, and driving technology solutions. The ideal candidate will have extensive experience in clinical trials, data management, and a strong proficiency with key technologies and regulatory standards. This role emphasizes leadership, collaboration, and innovation in transforming patient outcomes in autoimmune disease treatments.

Salary

Base: $200,000 - $225,000 USD annually; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Data Systems and Clinical Programming
  • AI-related initiatives for DM
  • EDC platform validation
  • SAS clinical programming
  • CDISC standards proficiency
  • clinical research regulations knowledge

Nice-to-have

  • continuous learning and growth
  • proactively identifying project challenges
  • innovative data management practices

Key Requirements

  • 12+ years of relevant experience
  • BS or equivalent degree
  • Experience supporting Ph I-IV clinical trials
  • Proficiency in CDISC standards
  • Experience with SAS, SQL
  • Proficiency in clinical research regulations

Work Rights

Not specified

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