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Lead Data Manager

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

College or University degree required, Minimum three years in Data Management, Two years as a Data Manager.

Key responsabilities:

  • Oversee all data management activities
  • Act as primary communication point
  • Coordinate data management activities in projects
  • Develop study documentation and manage data quality
  • Train Data Managers and Assistants
PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

Company Description

We’re over 2,700+ strong across the globe. We’re scientists, strategists, creatives, and innovators. We value individual brilliance and build a strong foundation for teamwork across all our business. We love the challenge of our industry. We’re changing lives and redefining success every step of the way.

You are dynamic. You are curious. You are more than your job. For you, excellence isn’t just a word; it’s the measure for all you do. You’re passionate. Driven. Dedicated. You can’t stand mediocrity. And you might be the team member we're looking for. 

Job Description

The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.

  • Acts as primary communication point for project teams and company departments regarding clinical data management
  • Acts as primary communication point for clients/vendors for all data management aspects of clinical projects
  • Coordinates data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables
  • Provides input into monitoring of project scope, budget, timelines, and deliverables
  • Is responsible for clinical data management activities including, but not limited to:
    • Development of study documentation (eCRF Requirements, Edit Checks Specification, Data Management Plan, CRF Completion Guidelines, User Access Management Plan, Data Validation Plan, External Data Transfer Agreements, SAE Reconciliation Guidelines, Local Lab Normal Ranges Guidelines, Coding Guidelines where applicable)
    • User acceptance testing
    • User access management
    • Data review
    • eCRF/External data reconciliation
    • Medical coding (for staff with medical/Life Science background)
    • SAE reconciliation
    • Query management
    • Study Database Lock activities
    • Archival of CRFs QC Coordination 
    • Project status reporting
    • Data listings/Patient profiles generation
  • Maintains and QCs TMF/eTMF as well as Data Management working files
  • Trains Data Managers and Assistant Data Manager
  • Conducts project-specific training

Qualifications
  • College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities 
  • Minimum of three years of industry experience in Data Management 
  • Two years in Data Manager role
  • This role requires travel on an as needed basis for client presentations, bid defense meetings, department meetings, and the like. 

Additional Information

All your information will be kept confidential according to EEO guidelines.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Training And Development
  • Timelines
  • Analytical Thinking
  • Verbal Communication Skills

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