Lead Data Manager

at  PSI CRO

Remote, Oregon, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Nov, 2024Not Specified18 Aug, 2024N/ATraining,TravelNoNo
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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

Responsibilities:

  • 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 trainin


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

IT Software - DBA / Datawarehousing

Clinical Pharmacy

Graduate

Proficient

1

Remote, USA