Centralized Study Associate II
Covance
Mumbai, MH, India
8h ago
source : CareerArc Group LLC

Job Overview :

  • Follow applicable departmental Standard Operating Procedures and Work Instructions.
  • Complete required trainings according to required timelines.
  • Manage day-to-day tasks ensuring quality and productivity.
  • Manage project and technical documentation in an appropriate manner.
  • Provide administrative and technical support to internal departments as needed.
  • Perform checks to ensure quality of work completed.
  • Ensure timely escalation and issue resolution.
  • Track and report metrics as determined by management according to required timelines.
  • Assist with the implementation of revised processes and procedures.
  • Other duties as assigned by management.
  • Manage clinical systems
  • Manage study documents Maintain study databases (CTMS, IWRS, EDC etc.
  • Education / Qualifications : Minimum Required :

    Years of experience in the job discipline : 2-3 Years

    Years of experience in other professional roles : 0-3 Years

    Other required work-related experiences :

  • Demonstrated ability to organize and communicate effectively.
  • Demonstrated ability to pay attention to detail.
  • Ability to work well with others.
  • Experience : Recommended :

    Universiry / College Degree (Life Science preferred) , or certification in a allied health profession from an appropriate accredited institution (E.

    g Nursing certification, Medical or laboratory technology) and 0-2 years of work experience in clinical research, including a strong working knowledge of the iCH guidelines and FDA,IRB / IEC regulations.

    In Lieu of the above requirement, candidate with one (1) or more years of relevant clinical research experience in Pharmaceutical or CRA Industries may be considered

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