Associate Director/Sr Clinical Data Manager

Description

Job title: Associate Director/Sr Clinical Data Manager

Company: Immunome, Inc.

Location: Bothell, Washington

Company Overview:

Immunome is a clinical-stage targeted oncology company committed to developing first- and best-in-class targeted therapies designed to improve outcomes for cancer patients. 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 targeted cancer therapies, including antibody-drug conjugate therapies (ADCs.) In addition to a portfolio of discovery-stage ADCs, our pipeline includes AL102, a gamma secretase inhibitor which is currently in a Phase 3 trial for treatment of desmoid tumors, as well as IM-1021, a ROR1 ADC, and IM-3050, a FAP-targeted radioligand, both of which are the subject of INDs expected to be submitted in the first quarter of 2025.

Position Overview:

The Senior Manager, CDM will be a highly motivated, quality-focused individual who can work collaboratively in a fast-paced, cross-functional team environment, and will oversee data management activities across multiple studies from study start-up through study closure in support of clinical trial objectives and corporate goals.

Key Responsibilities:

This position will be part of the cross-functional clinical trial team and be responsible for core deliverables such as clinical database design/setup, data collection, data validation, manual review, and timelines. All activities will be performed according to quality standards defined by regulations/standards, ICH-GCP. Responsibilities include:
 

• Act as the point of contact for DM activities for multiple trials, provide oversight of data collection and management per regulatory and industry standards.
• Provide oversight of the DM CRO and ensure performance against key indicators; provide DM expertise to trial teams
• Contributes to the development/review of relevant data management documentation, including but not limited to CRFs, CRF Completion Guidelines, Data Management Plans, Edit Check Specifications, Data Review Plans, Data Cleaning Plans, Data Transfer Specifications, etc.
• Review CRFs to ensure alignment with protocol; lead and perform sponsor acceptance testing of the eCRF; and ensure database structure meets expectations and provide DM insight to promote effective clinical database structure
• Performs DM lifecycle activities, from study start-up, maintenance, database lock and close-out. 
• Provide oversight of the data validation plan and provide DM insight to maximize the data validation strategy
• Define and perform data quality checks and take action to ensure data quality
• Provide oversight of key DM documentation and ensure inspection readiness; ensure documentation is aligned with best practices and provide improvement recommendations based on DM expertise
• Drive and support vendor qualification for data management; define/specify scope of work for functional tasks
• Participate in development of DM specific SOPs

Requirements

Educational Background: Bachelor’s degree in life sciences, pharmacy, or a related field.

Professional Experience: Minimum of 5 years of industry experience in clinical trial management within the biopharmaceutical industry

Knowledge and Skills:

• Very detail-oriented, thorough and organized
• Demonstrated project management experience with ability to perform under tight timelines and balancing conflicting priorities
• Versatile communicative and strong interpersonal skills
• Ability to work effectively in both a team setting and independently
• Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and recommended CDM Best Practices
• Knowledgeable in data privacy requirements for data collection of clinical trial data and information
• Proficient in Medidata Rave and/or other EDC platform study builds
• Experience working with and managing CROs/external vendors, 2+ years preferred
• Experience with writing SOPs, work instructions and guidelines preferred
• Experience with NDA/BLA activities preferred
• Experience with regulatory inspection/audit preparation preferred

E/E/O

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

Salary Range

$161,000 - $189,000