Clinical Data Specialist

IQVIA; Bengaluru; Hybrid; INR 1,200,000 - 1,800,000; Full time

Job summary

IQVIA in Bengaluru seeks a Clinical Data Specialist / Sr Clinical Data Coordinator with 3 to 6 years of experience to support CDM activities in a hybrid work environment. You will contribute data management expertise to ensure efficient, quality data products meeting customer needs.

The role involves supporting data operations, potentially leading data management tasks under supervision, and collaborating with the CDM team to meet project objectives.

Qualifications

• Experience in clinical data management environments.
• Experience with Rave or equivalent EDC is desirable.
• Familiarity with data quality processes and audits.

Responsibilities

• Serve as a Data Operations Coordinator (DOC) for one protocol with limited staff or for complex central studies, with guidance.
• May serve as back-up to a DOC or DTL.
• May write and resolve data clarifications.
• May lead database audit activities.
• May develop and test databases and edit specifications.
• May perform testing of programming and data coding tasks.

Skills

Rave

Core clinical data management

Study startup conduct & closeout

Reconciliation

UAT

Validation

Query management

DB Lock

Job description

Role: Clinical Data Specialist / Sr Clinical Data Coordinator

Work Experience: 3 to 6 years

Work Mode: Hybrid

Must Have Skills: Rave, Core clinical data management, Study startup conduct & closeout, Reconciliation, UAT, Validation, Query management, DB Lock

Job Overview:

Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.

Essential Functions :

• Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.
• May serve in the role of back-up to a DOC or DTL.
• May write and resolve data clarifications.
• May lead database audit team.
• May develop and test databases and edit specifications.
• May perform testing of programming.
• May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team.