Cognizant Data Specialist Jobs
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Cognizant Data Specialist Jobs For Life Sciences, Apply Online

Cognizant Data Specialist Jobs For Life Sciences, Apply Online. Life Sciences Process Specialist – Data position vacant for eligible candidates at Cognizant. Cognizant is hiring life sciences candidates for a Process Specialist – Data position. Interested and eligible candidates check out all of the details on the same below:

Job Title: Process Specialist – Data

Job ID: 00041440781

Location: Chennai, Tamil Nadu, India

Responsibility:

Business/ Customer:

  • Minimal Customer interaction under guidance.
  • Understands Domain Process/subprocess, functions, terminologies (such as SOP, QC checklists).

For PV/Complaints Management:

  • Individuals in this role perform data entry of data received from Source documents into the respective Clinical/Safety database While performing this activity the associate is responsible for meeting turnaround times and accuracy.
  • These associates are usually used to handle more critical/sensitive transactions.
  • These associates also act as Subject Matter Experts.

CODING:

Perform coding activities on the assigned project with timelines and efficiency

  • Import uncoded terms in the database and export coded medical terms from the coding platform.
  • Query Management.
  • Create “New Term Request” and prioritize.
  • Perform Dictionary up versioning activity.
  • Send Coding (Consistency) Reports.
  • Participate in study-related meetings as needed.
  • Provide feedback on quality-related issues to other medical coders in a timely manner.
  • Serve as an SME to Medical Reviewers regarding coding activities & guidelines.
  • Perform UAT for coding related applications.
  • Perform Operational QC.
  • Mentor Team Member.
  • Coordinate with CDM working on the same study.
  • Coordinate to resolve Rave specific issues.

CDM:

  1. Execute Data Management Activities ie Data Cleaning, Executing Manual and System checks, Update relevant trackers, Discrepancy and query management, Issue resolution, Database lock activities.
  2. Participate in innovation and process improvement initiatives.
  3. Identify and develop an action plan in coordination with the TL for activities not meeting the client SLAs.
  4. Archive all necessary information for audit purposes according to quality and security requirements, to ensure reliable and timely retrieval of documentation and information.
  5. Support multiple clinical trials, across diverse therapeutic areas, to successful conclusions and provide technical oversight when required.

Project / Process:

  • Attempts Complex problems (procedures/processes) and refers to Supervisor/Line Manager in rare cases.
  • Handle first-level processing of transactions.
  • Adhere to quality requirements, achieve targets/volumes in given TAT(Turn around time).
  • Proactively identify issues.
  • Contribute to process improvement initiatives.
  • Identify and report process changes.
  • Adhere to the mandatory industry regulation and compliance requirements for the given process

Knowledge Management:

  • Update Process documentation as appropriate for the process under guidance.
  • Participate in knowledge transfer.

People/Team Management:

  • Adhere to org hygiene and compliance needs in terms of.
  • a Personal Utilization & Time sheet submission.
  • b Personal and new hire Assimilation.
  • c Attendance.
  • d Team Initiatives.
  • Collate team performance metrics.
  • Manage break schedule/transport logistics for the team in the absence of his/her supervisor.

Qualification: Graduate/Post Graduate/ Doctorate degree in life sciences.

Must-Have Skills:

  • Clinical operations
  • Clinical Data Management

Employee Status: Full-Time Employee

Shift: Day Job

Travel: No

APPLY ONLINE

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