IQVIA Hiring For Clinical Data Specialist

Pharmabharat; India; On-site; INR 500,000 - 800,000; Full time

Benefits offered by this job

Exposure to global clinical trials

Career growth opportunities

Collaborative environment

Job summary

Pharmabharat is seeking a Clinical Data Specialist to support end-to-end Clinical Data Management activities in cities like Pune, Kolkata, and Thane. Candidates should possess a Bachelor's in Clinical, Biological, or Mathematical Sciences with 2-5 years of relevant experience.

This role involves reviewing clinical trial data, ensuring compliance with regulations, and requires hands-on experience with EDC platforms like Medidata Rave. Join us for a career in cutting-edge clinical research!

Qualifications

• 2-5 years of experience in Clinical Data Management (CDM).
• Strong understanding of the clinical trial lifecycle and clinical research processes.
• Experience in data review and query resolution.

Responsibilities

• Support end-to-end Clinical Data Management activities.
• Review and validate clinical trial data for accuracy and completeness.
• Collaborate with Data Operations Coordinators and other teams.

Skills

Clinical Data Management

Data review and query resolution

Medidata Rave

Attention to detail

Education

Bachelor’s Degree in Clinical, Biological, Mathematical Sciences or related field

Tools

Electronic Data Capture (EDC)

Job description

IQVIA Hiring For Clinical Data Specialist

Position: Clinical Data Specialist. Company: IQVIA. Job Type: Full-Time. Work Mode: Hybrid. Locations: Kolkata, Pune, Thane, Kochi, Bangalore, Hyderabad. Experience: 2-5 Years. Industry: Clinical Research / Clinical Data Management. Qualification: Bachelor’s Degree in Clinical, Biological, Mathematical Sciences or related field.

Key Responsibilities

• Support end-to-end Clinical Data Management activities.
• Review and validate clinical trial data for accuracy and completeness.
• Perform data review and query management activities.
• Resolve data discrepancies through data clarification processes.
• Work with Electronic Data Capture (EDC) systems such as Medidata Rave.
• Collaborate with Data Operations Coordinators (DOCs), Data Team Leads (DTLs), and Functional Managers.
• Ensure compliance with clinical research regulations and company standards.
• Support high-quality data delivery for global clinical studies.
• Participate in leadership and mentoring responsibilities within the CDM team.

Required Skills

• 2-5 years of experience in Clinical Data Management (CDM).
• Strong understanding of the clinical trial lifecycle and clinical research processes.
• Experience in data review and query resolution.
• Hands‑on experience with Medidata Rave or similar EDC platforms.
• Knowledge of medical terminology.
• Excellent organizational and communication skills.
• Strong attention to detail and quality-focused mindset.

This opportunity is specifically for professionals with Clinical Data Management experience. Profiles from Pharmacovigilance, Quality Control, Clinical Research Coordinator, or Programming backgrounds may not be suitable unless they possess relevant CDM experience.

Educational Qualifications

• Clinical Sciences
• Biological Sciences
• Mathematical Sciences
• Life Sciences
• Related Healthcare Disciplines

Equivalent relevant experience may also be considered.

Why Join IQVIA?

IQVIA offers professionals an opportunity to work on cutting-edge clinical research projects while developing their expertise in clinical data management.

Benefits

• Exposure to global clinical trials
• Career growth and leadership opportunities
• Collaborative and learning-focused environment
• Work with advanced clinical data management technologies
• Professional development within a globally recognized CRO

Job Locations

• Pune
• Kolkata
• Thane