Covance Clin Data Assoc III in Bangalore, India

Job Overview

Work concurrently on multiple data management projects, and with little to no guidance from functional manager/PDM

  1. Provide input and assistance in the design of Case Report Forms (CRFs).

  2. Able to assist study specific edit check specifications

  3. Assist in reviewing/writing/editing sections of the Data Management Plan and eCRF Completion Guidelines at the direction of the Project Data Manager

  4. Perform necessary interpretations of compare output and provide feedback to DM Project Leader for resolution and database edits in DM

  5. Reconcile project files, reports, listings and other documents generated in data management against a database for accuracy and completeness of data management processes. Assist with provision of data management reports in support for project team, Clinical Research Associates (CRAs), investigative sites, sponsor as requested.

  6. Demonstrate/describe data review processes to sponsors and auditors as and when needed

  7. Perform all tasks to relevant Chiltern and/or Sponsor SOPs, ICH or other regulatory guidelines in DM

  8. Work in a timely manner in accordance with all the activities specified in the agreed project budget, under the supervision and guidance of the Manager/ Project Data Manager

  9. Provide guidance and training to Level 1 and 2 CDA colleagues as well as new hires

  10. Perform other duties as required by the Department


Associate’s/BSc degree in biological science or a related discipline in the science/healthcare field or equivalent education


Minimum 2 -3+ years of CDA experience in CDM or Biostatistics in a CRO or pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job

Job Number 2019-28311

Job Category Clinical Data Management

Position Type Full-Time

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