Demo

External Data Acquisition Lead /Manager

Maxis Clinical Sciences
Boston, MA Contractor
POSTED ON 2/2/2025
AVAILABLE BEFORE 3/2/2025

 3 rd Party Data Acquisition Lead/Manager



  • Job Description:Serving as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level, managing study start up, conduct and close out activities.
  • Creating external data transfer agreements, ensuring external clinical trial data are in alignment with the Clent's Standards and specifications to support data integration, analysis, and reporting.
  • Help and advice in setting up infrastructure for external data , to flow into Client's Clinical data pipelines.
  • Responsible for validation of all 3 rd Party Data generated in clinical trial into Client's Clinical Data pipelines.
  • Developing strong and productive working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards and other Study Execution Team members.
  • Participates in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group in a formal inspection or audit.
  • Representing Client's in interactions with key external partners as part of Client's CT3 3 rd Party Data Acquisition team.
  • Responsible for timely submission and on-going maintenance of study related 3 rd Party Data Acquisition documentation in TMF.
  • Following procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes.
  • Liaising with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.) performing services on behalf of Client.
  • Escalating issues to CT3 leadership appropriately


  • Technical/Functional ExpertiseWorking knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles.
  • Experience with all phases of drug development .
  • Solid Experience in handling Clinical data acquisition and management from external/3 rd Party vendors
  • May lead study level negotiation and agreement for data transfer or integration on behalf of Client.

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