[Hiring] Senior Manager, Technical Clinical Data Management @Deciphera Pharmaceuticals

Role Description

We are seeking an experienced Senior Manager, Technical Clinical Data Management to take full accountability for end-to-end data management lifecycle activities across assigned clinical trials. In this dual-function role, the individual will serve as the primary Data Management Study Lead, managing timelines, cross-functional communication, risks, and deliverables while also applying hands-on technical expertise. Candidate will combine strong clinical data management leadership with the technical ability to design efficient, scalable solutions that improve data quality, accelerate issue resolution, and support timely study delivery.

Key Responsibilities:

• Clinical Data Management Leadership & Technical Operations
  • Represent Data Management on the Clinical Study Team, lead study communications, and manage expectations with the Data Management CRO.
  • Oversee all activities defined in the Data Management Plan (DMP) and ensure study deliverables meet quality and timeline expectations.
• Technical Operations
  • Advance vendor oversight by applying data intelligence to identify trends, strengthen performance monitoring, and improve operational efficiency.
  • Partner with IT to streamline external data transfers and integrate data across systems for cross-functional use.
• Vendor & Stakeholder Management
  • Oversee outsourced CDM vendors and ensure performance aligns with Deciphera standards.
  • Review vendor invoices as applicable.
  • Collaborate with cross functional team on data deliverables.
• Leadership, Process & Continuous Improvement
  • Enhance CDM processes and strengthen cross functional collaboration.
  • Support department initiatives as needed.
• Inspection Readiness, Quality & Metrics
  • Lead CDM inspection activities and manage findings to resolution.
  • Ensure CDM documentation is complete and filed in the TMF.
• Other duties and responsibilities as assigned.

Qualifications

• Bachelor's or master's degree with 8+ years of experience in Clinical Data Management.
• Knowledge of FDA/CFR and ICH/GCP.
• Familiarity of CDISC and CDASH standards.
• Experience with data visualization tools to build study-status and data quality dashboards.
• Experience creating and applying tools to clinical data workflows, including data review, automation, and visualization with appropriate validation and human oversight.
• Familiarity with AI (e.g. Copilot, Claude).
• Effective communication, organizational, and project management skills.

Requirements

• Experience building in Medidata RAVE.
• Hands on experience using SAS for data extraction and validation.
• Experience with J-Review.

Benefits

• Competitive salary and annual bonus.
• Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
• Generous parental leave and family planning benefits.
• Outstanding culture and opportunities for personal and professional growth.