Associate Director, Clinical Data Management
Location: San Francisco
Posted on: June 23, 2025
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Job Description:
Nurix Therapeutics is a clinical stage biopharmaceutical company
focused on the discovery, development, and commercialization of
targeted protein degradation medicines, the next frontier in
innovative drug design aimed at improving treatment options for
patients with cancer and inflammatory diseases. Powered by a fully
AI-integrated discovery engine capable of tackling any protein
class, and coupled with unparalleled ligase expertise, Nurix’s
dedicated team has built a formidable advantage in translating the
science of targeted protein degradation into clinical advancements.
Nurix aims to establish degrader-based treatments at the forefront
of patient care, writing medicine’s next chapter with a new script
to outmatch disease. Position Nurix has a place for an
extraordinary, highly motivated, self-starter and accomplished
Associate Director of Clinical Data Management to become a part of
the growing biometrics organization. Summary The Associate Director
of Clinical Data Management (CDM) will be responsible for the
delivery and integrity of clinical data across Nurix’s multiple
studies/programs. The role will also be supporting process
development and improvement in building clinical data management
infrastructure. He/She will ensure adherence to industry guidelines
in all clinical data management activities for assigned studies, as
well as assisting in the development and implementation of
departmental policies, operational guidelines, and administrative
structure. The successful candidate should have a successful track
record in managing vendors and effectively leading study clinical
data management activities with the anticipated growth in the
product pipeline. He/She must also possess excellent communication
skills work closely with medical study directors and clinical
operations to provide and receive direction to ensure high quality
and integrity in clinical data. Additional key representative
responsibilities will include, but not necessarily be limited to,
the following: Job Responsibilities: Lead and manage clinical data
management duties and tasks for assigned clinical trial from study
start up to study closeout Manage and provide oversight of vendors
(including clinical data management CRO) that have been contracted
to handle Nurix’s clinical data and ensure the data are complete,
accurate and delivered within the agreed upon timelines Ensure
inspection readiness by maintaining current documentation,
adherence to industry guidelines, SOPs and compliance with training
Work collaboratively with internal and external team members within
the study to coordinate the planning and execution of clinical data
management activities Create strategies for rapid study start and
database lock to increase clinical data management productivity
Lead the design of the eCRFs and ensure that they align with the
clinical protocol(s) Ensure complete and accurate documentation
such as eCRF specifications, eCRF completion guidelines, annotated
CRFs, data validation specifications, data transfer agreements, and
data management plans Ensure data is reviewed on an on-going basis,
including individual subject data within the EDC, datasets, TLFs,
etc. that are generated for CSRs, DSURs, IBs, and other business
needs Collaborate with clinical development team and provide
expertise regarding CDISC data standards, FDA and ICH guidelines,
and GCDMP standards Help establishing CDM processes and contribute
to the development of key clinical data management SOPs Provide
technical support and guidance for clinical data management team
and vendors around project conventions, standards, practices, and
database specifications Perform budget review and guidance for
clinical data management CRO for assigned trial Qualifications
Bachelor’s degree in a scientific discipline or equivalent
(computer science, mathematics, statistics, epidemiology, biology,
psychology). A Master’s degree in a related science field is
preferred Minimum of 10 years of clinical data management
experience within pharmaceutical industry with a track record of
success and progression for Associate Director level Minimum of 12
years of clinical data management experience within pharmaceutical
industry with a track record of success and progression for
Director level Direct experience working with Medidata Rave design
and implementation Proficient on regulatory requirements for
clinical data management and the regulatory submission process
Extensive experience working with external vendors, including but
not limited to acquisition, contracting, evaluation of vendor’s
capabilities and ensuring the desired high-quality deliverables
Demonstrated ability to operate and lead assigned study in a
dynamic organization, build successful working relationships and
effective stakeholder management in an environment that requires
diverse educational and functional expertise Able to adapt quickly
to the changing needs of the organization Able to organize multiple
work assignments and establish priorities Excellent verbal and
written communications skills; able to communicate proactively and
effectively Nurix Therapeutics, Inc. is committed to protecting and
respecting your privacy and personal information, including
information collected by Nurix when you apply for a job with Nurix
or in the course of your employment with Nurix. By applying for a
position at Nurix, you agree to our collection and use of personal
information as described in our Privacy Policy (
https://www.nurixtx.com/privacy-policy/ ).
Keywords: , San Bruno , Associate Director, Clinical Data Management, Science, Research & Development , San Francisco, California
