Insmed

Associate Director, Clinical Data Management

Insmed$164K — $213K *
US-AnywhereRemote in New Jersey, US
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 6+ years in clinical data management (biotech, pharmaceutical, or CRO environment)
  • 3+ years management experience
  • Hands-on experience with Electronic Data Capture (Medidata Rave required)
  • Experience in CRO and vendor management (including budgeting and auditing)
  • Proven experience developing study documents and SOPs
  • Familiarity with multiple phases of clinical development
  • Strong communication and collaboration skills for cross-functional team environments

Responsibilities

  • Review and revise Data Management study plans for quality and standardization
  • Manage data management activities with CROs and external vendors
  • Support regulatory submissions through data transfer preparations
  • Develop, review, and revise global SOPs while providing team training
  • Oversee design and development of electronic Case Report Forms (eCRFs)
  • Manage development and implementation of edit check specifications
  • Participate in monthly data reviews to ensure data accuracy and reliability
  • Facilitate study database locking based on predefined criteria and timelines

Benefits

  • Comprehensive medical, dental, and vision coverage
  • Annual wellbeing reimbursement and Employee Assistance Program (EAP)
  • Generous paid time off and caregiver support
  • 401(k) with competitive company match and annual equity awards
  • Access to company Learning Institute for professional growth
  • Employee resource groups and opportunities for community service
Full Job Description
About the Role:
We're looking for an Associate Director, Clinical Data Management on the Clinical Data Management (CDM) team to help us expand what's possible for patients with serious diseases. Reporting to the Head of Clinical Data Management, you'll 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 and data reconciliation. You will also provide SME support with Data Management related vendor audits, as well as authoring, review and revision of Insmed SOPs.

What You'll Do:

In this role, you'll 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. You'll 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


Who You Are:

You have a Bachelor's degree along with 6+ years of clinical data management experience in a biotech, pharmaceutical or CRO environment.

You are or you also have:
  • Three (3) years of prior management experience
  • Hands-on experience with Electronic Data Capture systems (Medidata Rave required) essential
  • Experience in CRO and vendor management required, 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


Nice to have (but not required):
  • Advanced degree


Where You'll Work

This is a fully remote role. It can be performed effectively from anywhere while staying connected to your Insmed team and community. Occasional travel for team meetings or events will be expected.

Travel Requirements

This role requires occasional domestic/international travel (approximately 15%)

#LI-JK

#LI-Remote

Pay Range:
$164,000.00-213,000.00 Annual

Life at Insmed

At Insmed, you'll find a culture as human as our mission-intentionally designed for the people behind it. You deserve a workplace that reflects the same care you bring to your work each day, with support for how you work, how you grow, and how you show up for patients, your team, and yourself.

Highlights of our U.S. offerings include:
  • 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 with purposeful in-person collaboration
  • 401(k) plan with a competitive company match, annual equity awards, and participation in our Employee Stock Purchase Plan (ESPP), and 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


Eligibility for specific programs may vary and is subject to the terms and conditions of each plan.

Current Insmed Employees: Please apply via the Jobs Hub in Workday.

About Insmed

Insmed is a biopharmaceutical company that develops drugs to treat serious and rare diseases. The company's lead product candidate is ARIKAYCE, which is being developed to treat patients with nontuberculous mycobacterial lung disease. Insmed is also developing drugs to treat other respiratory diseases, as well as rare diseases such as lipodystrophy. The company was founded in 1988 and is headquartered in Bridgewater, New Jersey.
Learn more about Insmed
Size
613 employees
Market Cap
$2.6 billion
Industry
Net Income
-$294 million
Revenue
$164.4 million
NASDAQ

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