Associate Director, Clinical Data Management

Associate Director, Integrated Drug Substance Development

Associate Scientist I, Immunology

Associate Scientist, Analytical Development

Associate Scientist, Exosome Production Core

Clinical Trial Associate

Director of Finance/ Controller

Director, Clinical Data Management

Director, Head of FP&A

Director, Legal

Director, Oncology Research

Facility Manager

In Vivo Scientist

Manager / Director of Technical Accounting and Financial Reporting

Manager/Sr. Manager, Quality Assurance

Principal Associate Scientist, Analytical Development

Principal Associate Scientist, Integrated Drug Substance Development

Quality Control Supervisor

Scientist I, Discovery Research

Scientist I, Immunology

Scientist I/II, Discovery Research

Scientist I/II, Molecular and Cellular Biology

Scientist II, Immunology

Scientist II, Integrated Drug Substance Development

Scientist/Sr. Scientist, Cell Assays/Analytical Development

Senior Associate Scientist, Integrated Drug Substance Development

Senior Associate Scientist, Process Sciences

Senior Clinical Project Manager

Senior Director/ VP Clinical Development Immuno-oncology

Sr. Accountant

Sr. Associate Scientist, Oncology

Sr. Director Legal, Intellectual Property

Systems Engineer

Technical Support Engineer

Vice President, Head of Analytical Development

Codiak BioSciences

published

The Associate Director, Clinical Data Management (CDM) is responsible for data management tasks from study start-up, database design, data quality and documentation through database lock. Responsibilities also include assisting with the creation of CRFs, actively participating in User Acceptance Testing (UAT), data cleaning, query generation and management, and assisting in the review of relevant data management documents.

Full Time

expired