Centralized Study Associate II (Clin Ops) @ Covance Location Bangalore, India
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
Covance is proud to be an Equal
Opportunity Employer:
Covance is an equal opportunity
employer and will not discriminate against any employee or applicant for
employment because of race, color, religion, sex, sexual orientation, gender
identity, national origin, disability, or veteran status.
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