SME-Clinical Data Management

Cognizant; Maharashtra; On-site; INR 600,000 - 1,100,000; Full time

Job summary

Cognizant in Maharashtra is seeking a Data Management Specialist to execute data management activities in clinical trials, including data cleaning and system checks, while updating trackers and resolving discrepancies. You will collaborate with a team lead to ensure SLAs, participate in process improvements, and archive information for audits, across multiple therapeutic areas.

Experience with RAVE/VEEVA EDC and Spotfire is valued.

Qualifications

• Experience in clinical data management and data cleaning.
• Ability to coordinate with TL and clients to address SLAs.
• Familiarity with audit trails and regulatory documentation.
• Experience handling third-party data (lab, PK, image) is a plus.
• Strong communication and problem-solving skills.

Responsibilities

• Execute data management activities: data cleaning, manual and system checks, and tracker updates.
• Manage discrepancies and queries; resolve issues to meet client SLAs.
• Archive documentation for audit trails per quality and security requirements.
• Support multiple clinical trials across therapeutic areas; provide technical oversight.
• Gain hands-on experience in study setup.
• Work with RAVE/VEEVA EDC and Spotfire reporting tools.
• Handle third-party data (lab, PK, images); maintain client communication.

Skills

Data management

Quality control

Client communication

Process improvement

Discrepancy management

Audit readiness

Tools

RAVE

VEEVA EDC

Spotfire

Job description

1. 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. 2 Participate in innovation and process improvement initiatives.
3. 3 Identify and develop action plan in coordination with the TL for activities not meeting the client SLAs.
4. 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. 5 Support multiple clinical trials, across diverse therapeutic areas, to successful conclusion and provide technical oversight when required.
6. 6 Study Setup hands on experience.
7. 7 Working exposure in RAVE/VEEVA EDC, Knowledge of Spotfire reporting tool ,
8. 8 Third party data handling experience (Lab, PK, Image etc), Client facing role (experience in client communication