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Lead Clinical Research Associate (CRA) Job Req. # 30733

Eingestellt von Novo Nordisk

Gesuchte Skills: Support

Projektbeschreibung

PURPOSE:
Responsible for the performance of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines and federal regulations. Responsible for operational aspects of planning and management of site performance in accordance with departmental productivity expectations. Acts as primary liaison between In-House CRAs, Field Based CRAs and the PM for assigned sites. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR.

RELATIONSHIPS:
Reports to an Associate Director/Senior Manager/Manager of Site Management (SM) within CTM. Accountable for actively participating in multiple internal cross-functional teams locally to ensure the effective delivery of assigned project milestones. External relationships are with clinical investigators, Contract Research Organizations (CROs), and other clinical research vendors as needed to support business objectives for the department and/or function.

ESSENTIAL FUNCTIONS:

COORDINATION / COMMUNICATION, ADMINISTRATION AND PERSONNEL DEVELOPMENT:
- Ensure compliance with the application and communication of all Novo Nordisk® policies, procedures and fundamentals.

FUNCTIONAL SUPPORT:
- May participate in continuous improvement processes for function.

Projektdetails

  • Einsatzort:

    Princeton, Vereinigte Staaten

  • Projektbeginn:

    asap

  • Projektdauer:

    Keine Angabe

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    Sonstiges

  • Skills:

    support

Novo Nordisk