Assoc Medical Data review Manager

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

Job summary

IQVIA is hiring for an Associate Medical Data Review Manager in Bangalore/Thane. The role involves reviewing patient-reported data, identifying anomalies, and coordinating data quality initiatives in a hybrid setup.

The position requires MBBS/MD and 2+ years of experience in clinical data sciences, with leadership exposure and strong data management skills. You will collaborate across clinical teams and sites to ensure data integrity and audit readiness.

Qualifications

• Good understanding of clinical/medical data.
• Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.
• Proven leadership in clinical data sciences.

Responsibilities

• Serve as a Subject level Data reviewer (SLDR) and identify anomalies in patient-reported data.
• Conduct in-stream data trend analysis to support data quality and integrity.
• Provide project management and act as SME in data management.

Skills

Medical data

Clinical data sciences

Leadership

Data review

Education

MBBS/MD

Job description

Job Title / Primary Skill: Associate Medical Data Review Manager

Years of Experience: 2 + Years.

Job Location: Bangalore/Thane (Hybrid)

Educational qualification: MBBS/MD is a must.

Job Overview:

• Serve as a Subject level Data reviewer (SLDR) and identify any anomalies in patient reported data by performing Subject
• Level Data Review that requires further investigation with the clinical site to determine overall accuracy
• Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
• Provide project management to the team in the area of Project Management and viewed as an expert in data management.
• Drive the delivery of end-to-end study data quality and integrity.
• Provide medical, clinical, and scientific advisory expertise.
• May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings.
• Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. .
• Define data capture requirements in line with protocol and reporting needs.
• Maintain strong customer relationships
• Ensure timely follow-up and resolution of compliance issues
• Serve as Subject Matter Expert (SME)
• Serve as POC/ Back-up POC

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Good understanding of clinical/medical data.
• Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.
• Proven expertise in the proactive identification of issues.
• Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics.
• Proven ability to work within a matrix team environment requiring minimum level of supervision

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• MBBS or MD with 2 + years of work experience.
• Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience