Top 3 Skill Sets Needed :
• 5+ years experience in clinical data management in the pharmaceuticals/biotechnology setting (ideally at with a sponsor) working with CRO oversight
• Hands-on working knowledge / Experience with Electronic Data Capture (EDC) systems (RAVE ideal)
• Ability to manage multiple projects at once and work effectively in a team dynamic
Responsibilities include:
• Collaborate with cross-functional working groups/teams to define new/enhance existing processes for data management activities.
• Influence procedures and processes and how they relate to functional partners such as Global Study Management, Site Management, and Global Biomedical Science.
• Oversee assigned activities as required by the working group/team/manager.
• Ensure that Global Study Operations Data Management (GSO-DM) procedures and processes are adhered to and meet business requirements.
• Accountability for meeting assigned timelines.
• Risk management of assigned projects.
• Point of contact for escalation of issues within the assigned projects.
• Lead activities for assigned project team.
• Communicate with a wide audience both with assigned team and cross-functionally.
• Review related documents and process maps within a project area, ensure consistency and accuracy of content.
• Represent data management on assigned project teams.
• Promote and be an advocate of Data Management internally and externally.
Skills:
• The ideal candidate should have extensive experience in clinical data management activities within the biotechnology or pharmaceutical industry.
• Strong leadership, organizational and communication skills are required.
• Previous process improvement experience and able to contribute to Client ideas in improving processes are also required of the candidate.
• Direct oversight experience is required and intimate knowledge of data management life cycle is essential for the candidate.
• 5+ years experience in clinical data management in the pharmaceuticals/biotechnology setting (ideally at with a sponsor) working with CRO oversight
• Hands-on working knowledge / Experience with Electronic Data Capture (EDC) systems (RAVE ideal)
• Ability to manage multiple projects at once and work effectively in a team dynamic
Responsibilities include:
• Collaborate with cross-functional working groups/teams to define new/enhance existing processes for data management activities.
• Influence procedures and processes and how they relate to functional partners such as Global Study Management, Site Management, and Global Biomedical Science.
• Oversee assigned activities as required by the working group/team/manager.
• Ensure that Global Study Operations Data Management (GSO-DM) procedures and processes are adhered to and meet business requirements.
• Accountability for meeting assigned timelines.
• Risk management of assigned projects.
• Point of contact for escalation of issues within the assigned projects.
• Lead activities for assigned project team.
• Communicate with a wide audience both with assigned team and cross-functionally.
• Review related documents and process maps within a project area, ensure consistency and accuracy of content.
• Represent data management on assigned project teams.
• Promote and be an advocate of Data Management internally and externally.
Skills:
• The ideal candidate should have extensive experience in clinical data management activities within the biotechnology or pharmaceutical industry.
• Strong leadership, organizational and communication skills are required.
• Previous process improvement experience and able to contribute to Client ideas in improving processes are also required of the candidate.
• Direct oversight experience is required and intimate knowledge of data management life cycle is essential for the candidate.