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Senior Manager, Data Management

ORIC Pharmaceuticals
San Diego, CA Full Time
POSTED ON 2/13/2025
AVAILABLE BEFORE 5/13/2025

Job Description

Job Description

Company Description

ORIC is a research-driven company dedicated to discovering and developing novel therapies that can Overcome Resistance In Cancer. Our collaborative, empowering culture gives scientists the authority, responsibility, and support to do cutting-edge work on therapies for treatment-resistant cancers. Our culture and values support our mission, provide a shared understanding of how we work together as a company and provide a clear sense of what is most important for us as an organization.

Job Description

We are seeking a Senior Manager, Data Management to join our team in San Diego or remotely. In this role, you will lead the development and implementation of enterprise-wide data management strategies while ensuring data quality, security, and compliance across the organization.

Essential duties and responsibilities include the following.  Other duties may be assigned.

  • Primary data management point of contact for the CRO(s) DM activities and deliverables in conjunction with the study teams. Ensures project deliverables and proposes solutions for data management issues that arise during assigned studies.
  • Work within the clinical study teams for all assigned studies and liaise directly with internal functions within Clinical Development, Clinical Operations, Pharmacovigilance, Biostatistics, and other functions, as well as external vendors to coordinate all aspects of data management
  • Participate in data management CRO and technology evaluations, qualifications, selections, and implementations
  • Assist in the development, vetting and finalization of study timelines, related to data management
  • Review, provide comments and finalize the CRF specifications, EDC entry screens, edit check specifications and data cleaning plan, CRF completion guidelines (CCGs), data transfer agreements (DTAs), Coding Plan, Communication Plan, UAT Plan and various other documents related to data management, in coordination with the CRO(s)
  • Provide input and comments to protocols, ePRO set-up, and IXRS development
  • Review, provide comments and finalize the Data Management Plan, in coordination with the CRO(s)
  • Perform User Acceptance Testing (UAT) on the proposed final version of the EDC and completed associated documentation
  • Perform manual data review, communicate associated queries and track to resolution
  • Oversee vendor data transfers and ensure timely reconciliation of all external data, in coordination with the CRO(s)
  • Coordinate database lock timelines, perform all sponsor related activities to achieve a successful and on-time database lock
  • Attend and participate in all team meetings both internal and external for assigned studies to ensure consistency in communication and timely delivery of tasks
  • Perform all duties in keeping with the Company’s core values, policies and all applicable regulations

Qualifications

  • BA / BS with science major (12 years’ experience), MS (8 years’ experience), PhD (5 years’ experience), or an equivalent combination of education with relevant Oncology experience in data management in pharmaceutical / biotechnology company or CRO including trial set-up, maintenance, and close-out of US and non-US trials at all phases of pre-NDA clinical research (Phases 1-3)
  • Must be able to thrive in an entrepreneurial, fast-paced, and dynamic work environment
  • Must be organized and be able to communicate effectively
  • Demonstrated excellence in trial management skills, with track record of successfully managing multiple projects, trials, and priorities
  • Additional Information

    The anticipated salary range for l candidates is between $120,000-$160,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc.  ORIC is a multi-state employee, and this salary range may not reflect positions that work in other states.

    ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristic.

    Salary : $120,000 - $160,000

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