Wipro Life Sciences Associate Job – Biotech, Microbio, Genetics, Bio-Engineering Candidates Apply
Wipro Life Sciences Associate Job – Biotech, Microbio, Genetics, Bio-Engineering Candidates Apply. Wipro BSc Jobs. Wipro MSc Jobs. Life Sciences jobs at Wipro. Interested and eligible applicants can check out all of the details on the same below
Associate
Locations: Gurugram, India
Categories: DOP
Req ID: 2973983
Job Description
- To evaluate structured and unstructured data generated by the program, including source documents (e.g. faxes and emails) for Reportable Safety Information (“RSI”).
- To assess source documents and complete a Primary review of the information to detect for missed RSI.
- Correct entries in relevant fields of the Client Application
- Accurately fill up the CEP forms for RSI, with all available verbatim source information
- Perform redaction activities and upload redacted files on WIPRO FTP on monthly basis, if needed
- Timely completion of Wipro and Client training
- Maintain training files
Roles & Responsibilities:
Organizational responsibilities:
- Ensures Wipro assigned training are completed within the timelines.
- Ensure compliance with Wipro policies and procedures.
- Ensures timely submission of Goals and Objectives.
- Ensures Floor Policy is signed, followed and any deviation noted is immediately notified to Supervisor/Risk and Compliance department
Qualifications:
- A certification from the country where the service is being provided, as a licensed pharmacist, licensed physician/dentist, licensed registered nurse and/or Life Science graduate Degree. All registered nurses must have completed clinical training as part of their licensing.
or - A Life Sciences graduate should have a Bachelor’s Degree in one of the streams like Biotechnology, Microbiology, Chemistry, Genetics, Bio-Engineering
Technical Competencies:
- Knowledge of US and EU regulations and guidelines for Pharmacovigilance.
- Excellent understanding of medical terminology and familiarity with principles of clinical assessment of adverse events in the context of an international pharmaceutical industry.
- Ability to independently resolve routine problems related to case creation/Source doc and surface issues constructively.
- Demonstrated computer literacy, particularly in the use and management of relational databases.
- Ability to manage one’s own productivity, time management, quality, and compliance in order to achieve acceptable results within given timelines.
- Ability to achieve personal objectives while meeting departmental standards of performance.
- Ability to work under supervision in a matrix organization.
- Ensure training and understanding of case processing SOPs/guidelines/tools.
- Prioritize cases as appropriate or as directed by the Client.
- Analyze special requests for case processing.
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