SME-Clinical Data Management

Cognizant; Kolkata District; On-site; INR 600,000 - 750,000; Full time

Job summary

Cognizant in India is seeking a Data Management professional to support CDM activities, including data cleaning, checks, and discrepancy management. You will archive data for audits, assist in multiple clinical trials, and contribute to process improvements.

Exposure to RAVE/VEEVA EDC and Spotfire is preferred, with strong startup knowledge and client-facing duties. Role involves collaboration with the TL to address SLAs, and hands-on study setup experience, contributing to reliable data

Qualifications

• Startup knowledge is a must.

Responsibilities

• Execute Data Management activities: data cleaning, manual and system checks, update trackers, discrepancy and query management, issue resolution.
• Archive information for audit purposes per quality and security requirements.
• Support multiple clinical trials across diverse therapeutic areas to successful conclusion.
• Identify and develop action plans with the TL for activities not meeting client SLAs.
• Participate in innovation and process improvement initiatives.
• Study setup hands-on experience.
• Working exposure in RAVE/VEEVA EDC.
• Knowledge of Spotfire reporting tool.
• Third party data handling experience (Lab, PK, Image) for client-facing communications.

Skills

Data cleaning

Client facing

Process improvement

Audit readiness

Tools

RAVE/VEEVA EDC

Spotfire

Job description

JD CDM:

1 Execute Data Management Activities I.e., Data Cleaning, Executing Manual and System checks, Update relevant trackers, Discrepancy and query management, Issue resolution, Database lock activities.

2. Start up knowledge is must.

3 Participate in innovation and process improvement initiatives.

4 Identify and develop action plan in coordination with the TL for activities not meeting the client SLAs.

5 Archive all necessary information for audit purposes according to quality and security requirements, to ensure reliable and timely retrieval of documentation and information.

6 Support multiple clinical trials, across diverse therapeutic areas, to successful conclusion and provide technical oversight when required.

7 Study Setup hands on experience.

8 Working exposure in RAVE/VEEVA EDC, Knowledge of Spotfire reporting tool ,

9 Third party data handling experience (Lab, PK, Image etc), Client facing role (experience in client communication