Data Management Contractor

Alumis•South San Francisco, CA

1d•Hybrid

About The Position

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. The Data Management (DM) Contractor will be responsible for ensuring high-quality management of clinical trial data in a rapidly evolving environment, in accordance with industry standards. The DM Contractor will support and/or lead DM activities and deliverables across one or multiple studies.

Requirements

10+ years of relevant experience and has earned a BS or equivalent degree; MS or MBA a plus
Experience running Ph I-IV clinical trials, both in-house and through CRO partners
Strong knowledge and experience in EDC and other key technologies (e.g., IXRS, data visualization)
Proficiency in CDISC standards (CDASH, SDTM, ADaM)
Experience with SAS, SQL and/or other clinical programming tools
Proficiency in clinical research regulations and guidance, including FDA CFR and ICH GCP
Depth of experience across all aspects of DM, including but not limited to: CRF and database development, data quality assurance and analytics, data transfer management, vendor management, DM study documentation and inspection readiness.
Strong understanding of the application of MedDRA and WHO Drug clinical data coding classification systems
Strong interpersonal, organizational, and communication (oral and written) skills
Demonstrated ability to cultivate strong working relationships with internal and external colleagues.
Logical thinking, attention to detail and accuracy, strong organizational skills, and problem-solving abilities
Ability to prioritize and to adapt quickly to changing business conditions with a “can-do” attitude
Capable of proactively identifying project challenges and risks and proposing appropriate and strategic solutions to issues.

Responsibilities

May serve as DM Study Lead or DM support for one or more studies
Represent DM in cross-functional meetings as applicable
Ensure DM project deliverables are completed on time and in accordance with quality standards and regulatory requirements from study start-up through study closure/archival
Apply effective vendor management throughout the study
Responsible for ensuring complete and accurate DM documentation such as eCRF specifications, eCRF completion guidelines, annotated CRFs, data validation specifications, data transfer agreements and data management plans
Perform thorough development testing of the eCRF prior to deployment, inclusive of creating User Acceptance Test (UAT) Plans, Test Scripts and executing testing as applicable
Ensure accurate development and execution of data integrations between EDC, IXRS and/or external vendor data sources
Responsible for setup and management of data transfers for assigned studies, including review of test data transfers for consistency with data transfer agreements
Participate in study document reviews, e.g. clinical study protocols, statistical analysis plans, Mock Tables, Figures and Listings (TFL) shells
Perform supplemental data reviews according to the data quality checks outlined in the data validation specifications or Clinical Data Review Plan (CDRP)
Participate in reviews of blinded TFL output prior to final database locks
Report query trends and data/query/SDV metrics to the Study Execution Team (SET)
Participate in the development of EDC custom report specifications, SAS Clinical Programming report specifications and/or associated outputs as needed
Ensure DM project documentation is in an inspection-ready state