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Deciphera Pharmaceuticals

Develops kinase inhibitors for cancer.

Senior Manager - Technical Clinical Data Management

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeWaltham, MA, USARemote

About the Job

Requirements

  • A bachelor's or master's degree and at least 8 years of experience in Clinical Data Management.
  • Knowledge of FDA/CFR and ICH/GCP.
  • Familiarity with CDISC and CDASH standards.
  • Experience using 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 artificial intelligence tools such as Copilot or Claude.
  • Effective communication, organizational, and project management skills.

Responsibilities

  • Take full accountability for end-to-end data management lifecycle activities across assigned clinical trials, serving as the primary Data Management Study Lead while managing timelines, cross-functional communication, risks, and deliverables, and applying hands-on technical expertise.
  • Represent Data Management on the Clinical Study Team, lead study communications, and manage expectations with the Data Management CRO.
  • Oversee activities defined in the Data Management Plan and ensure study deliverables meet quality and timeline expectations.
  • Apply data intelligence to identify trends, strengthen performance monitoring, and improve operational efficiency in vendor oversight.
  • Partner with IT to streamline external data transfers and integrate data across systems for cross-functional use.
  • Oversee outsourced clinical data management vendors and ensure their performance aligns with company standards.
  • Review vendor invoices as applicable.
  • Collaborate with the cross-functional team on data deliverables.
  • Enhance clinical data management processes and strengthen cross-functional collaboration.
  • Support department initiatives as needed.
  • Lead clinical data management inspection activities and manage findings to resolution.
  • Ensure clinical data management documentation is complete and filed in the Trial Master File.
  • Perform other duties and responsibilities as assigned.

Desired Qualifications

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

About the Company

Deciphera Pharmaceuticals

Develops kinase inhibitors for cancer.

Deciphera is a biopharmaceutical company focused on discovering, developing, and commercializing cancer medicines. It uses a proprietary switch-control kinase inhibitor platform and deep kinase biology expertise to create targeted therapies for various cancers. The company advances drug candidates through research, clinical trials, and regulatory approval, then brings approved medicines to market and seeks partnerships or licensing deals to expand its reach. Its competitive edge comes from its unique switch-control kinase inhibitors and deep biology know-how, which aim to deliver precision treatments in oncology. The company’s goal is to improve the lives of cancer patients by delivering effective targeted therapies.

Company size
501-1,000
Company stage
IPO
Headquarters
Waltham, MA
Founded
2003

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