Senior Clinical Data Manager

Company Overview

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, drawing on leadership that previously played key roles in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugate therapies. Our pipeline includes varegacestat, a late-clinical stage GSI; IM-1021, a clinical-stage ROR1 ADC; and IM-3050, a FAP-targeted radiotherapy that recently received IND clearance. We are also advancing a broad portfolio of early stage ADCs pursuing undisclosed solid tumor targets.

Position Overview

The Senior Clinical Data Manager (Sr. CDM) is responsible for leading end-to-end data management activities across one or more complex clinical trials. This role ensures high-quality, reliable clinical data that meets regulatory standards and supports timely clinical development decisions. The ideal candidate is a proactive problem solver with experience in data standards, EDC systems, and cross-functional collaboration.

Responsibilities

Study Planning & Start-Up

• Serve as the data management lead for assigned clinical studies, providing strategic input into protocol design and data collection strategy.


• Develop and manage Data Management Plans (DMPs), CRF/ eCRF specifications, edit check specifications, and data validation plans.


• Lead EDC system set-up, UAT, and deployment; coordinate with external vendors and internal biometrics teams.

Execution & Oversight

• Oversee all data review activities, including query management, data cleaning, discrepancy resolution, and ongoing data quality monitoring.


• Ensure adherence to CDISC/CDASH/SDTM standards where appropriate, as well as applicable regulatory requirements (ICH-GCP, FDA, EMA).


• Track study metrics, identifying risks and implementing mitigation strategies to maintain high-quality and timely deliverables.


• Manage interactions with CROs, central labs, imaging vendors, and other data contributors.

Close-Out & Reporting

• Lead database lock activities, ensuring audit readiness and complete documentation.


• Support statistical programming and medical writing teams in delivering data for interim analyses, CSR outputs, and regulatory filings.


• Contribute to process improvements and knowledge sharing within the data management function.

Qualifications

• Bachelor’s degree in relevant field


• A minimum of 5 years of Clinical Data Management experience in the biotech/pharma industry. Oncology experience is strongly preferred.

Knowledge and Skills

• Demonstrated expertise with EDC systems (e.g., Medidata Rave, Oracle InForm, Veeva CDMS).


• Understanding of clinical trial methodology, regulations, and data standards.


• Experience leading data management activities for Phase I–III global clinical trials.


• Vendor oversight experience and ability to drive cross-functional alignment.


• Knowledge of FDA, ICH-GCP, and 21 CFR Part 11 compliance.


• Excellent communication, documentation, and project management skills

E/E/O

Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

E-Verify

Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).