For PV/Complaints Management Individuals in this role perform data entry of data received from Source documents into the respective Clinical/Safety database While peroforming this activity the associate is responsible for meeting turnaround times and accuracy.
Coding
(same as SPE)
Perform coding activities on the assigned project with timelines and efficiency.
Import uncoded terms in database and export coded medical terms from coding platform.
Query Management.
Create “New Term Request” and prioritize.
Perform Dictionary upversioning activity as and when required.
Cdm
Limited to study conduct activities.
Data review and Query management is done with assistance.
Limited email conversations with Client.
Every activity requires Peer QC by supervisor or allocated seniors.
NO INVOLVEMENT in Set Up and Migration activities.
Limited involvement of data pad locking activities during timelines of DataBase locks.
Project / Process
Handles First level processing of assigned transactions, Complex problems (procedures/processes) are referred to Supervisor/Line Manager.
Adhere to quality requirements, achieve targets/volumes in given TAT(Turn around time).
Adhere to the mandatory industry regulation and compliance requirements for the given process.
Knowledge Management
Understand various document templates and standards(Such as SOP's) to interpret the documents & related terminologies.
People/Team Management
Adhere to org hygiene and compliance needs in terms of Time sheet submission, Assimilation & Attendance.
Must Have Skills
Generative AI
Good To Have Skills
Pharmacovigilance&Safety Ops
Seniority level
Entry level
Employment type
Full-time
Job function
Business Development and Sales
Industries
IT Services and IT Consulting and Business Consulting and Services
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