Assoc Medical Data Review Mgr

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

Job summary

IQVIA in Bengaluru, India, seeks a Medical Review professional to provide comprehensive data management and project management support from a clinician's perspective. The role emphasizes ensuring data quality and medical plausibility across study datasets.

You will work as a Subject Matter Expert, collaborating with clinical study teams and clients to drive process improvements while maintaining strong relationships and delivering high-quality deliverables.

Qualifications

• MBBS or MD with clinical data experience.
• Experience in CRO/pharma with leadership responsibilities.
• Strong understanding of clinical/medical data.
• Knowledge of medical terminology, pharmacology, anatomy, physiology.
• Excellent communication and teamwork skills.
• Ability to manage multiple projects with minimal supervision.

Responsibilities

• Identify patient anomalies to ensure data plausibility.
• Provide project management with study teams for process improvements.
• Maintain strong customer relationships.
• Track service performance and drive root-cause actions.
• Resolve compliance issues in a timely manner.
• Serve as Subject Matter Expert (SME).
• Look for efficiency and quality improvements.
• Provide therapeutic area training for the project team.
• Attend Kick-Off, weekly team, and client meetings.

Skills

Project management

Leadership

Communication

Teamwork

Customer service

Problem solving

Education

MBBS

MD

Job description

Job Overview

Provide comprehensive Medical Review expertise to provide efficient, quality data management products that meet customer needs. Provide project management support in the areas of structured patient data review per clinician's perspective.

Essential Functions

• Identify patient anomalies to ensure medical congruency/plausibility of a subject data per protocol.
• With minimal guidance, provide project management expertise working with clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
• Maintain strong customer relationships
• With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions
• Ensure timely follow-up and resolution of compliance issues
• Serve as Subject Matter Expert (SME)
• Continuously look for opportunities to improve efficiency of tasks and quality of deliverables
• Provide therapeutic area/indication training for the project clinical team.
• Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.

Qualifications

• Medic (MBBS) with 2+ years of Experience or MD with any experience/Fresher
• Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience Req
• Good understanding of clinical/medical data.
• Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology
• Must have Medical but also an operational focus towards metrics and status information to take the appropriate actions to resolve.
• Excellent communication, interpersonal, customer service, and teamwork skills
• Excellent organizational and problem-solving skills
• Excellent project management skills and coaching skills
• Ability to work with minimal supervision, using available resources,
• Ability to work on multiple projects and manage competing priorities
• Strong customer focus skills
• Ability to establish and maintain effective working relationships with coworkers, managers and clients

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.