01Overview
Role Description
Were looking for an Associate Director, Clinical Data Management on the Clinical Data Management (CDM) team to help us expand whats possible for patients with serious diseases. Reporting to the Head of Clinical Data Management, youll be responsible for working in conjunction with the Clinical Project Manager and study team to ensure data review, project support, study document management and CRO oversight of:
DM timelines
EDC/IWRS set up
Study database design
Clinical data capture
Discrepancy management
Data reconciliation
You will also provide SME support with Data Management related vendor audits, as well as authoring, review and revision of Insmed SOPs.
In this role, youll have the opportunity to review and provide input into protocols to ensure the data collection, database and reporting requirements can be met and are standardized across the programs. Youll also:
Review/revise Data Management related study plans including Data Management Plan, Data Validation Plan and other study documents to ensure quality and standardization
Manage and oversee data management related activities with CROs and other external vendors
Work with vendor(s) in preparation of regulatory submissions, particularly to support the DM tasks such as transfer of data
Develop, review and revise global SOPs providing team training where applicable
Manage design and development of eCRFs, clinical review and communication with CRO
Oversee and manage the development and implementation of edit check specifications and work with CRO during programming & validation
Participate in monthly data reviews with clinical team to ensure accuracy, consistency and reliability of data
Work with CROs and study teams to ensure study databases are locked based on pre-defined criteria and timelines
Ensure that CDM procedures and processes meet business requirements and are adhered to in a consistent manner
Provide high quality services through efficient and compliant processes
Qualifications
Bachelors degree
Minimum years of clinical data management experience in a biotech, pharmaceutical or CRO environment
Three (3) years of prior management experience
Hands-on experience with Electronic Data Capture systems (Medidata Rave required)
Experience in CRO and vendor management, including vendor budgeting and auditing
Experience in developing study documents and SOPs
Experience with multiple phases of clinical development
Excellent communication skills and ability to work in a cross-functional team environment
Strong collaboration skills regarding external and internal teams
Requirements
Nice to have: Advanced degree
Benefits
Comprehensive medical, dental, and vision coverage and mental health support
Annual wellbeing reimbursement and access to our Employee Assistance Program (EAP)
Generous paid time off policies, fertility and family-forming benefits, caregiver support, and flexible work schedules
401(k) plan with a competitive company match, annual equity awards, and participation in our Employee Stock Purchase Plan (ESPP)
Company-paid life and disability insurance
Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities
Employee resource groups, service and recognition programs, and meaningful opportunities to connect, volunteer, and give back
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Company : Insmed Incorporated
Salary : Work from home .