Assoc Medical Data review Manager

IQVIA

Bengaluru

On-site

USD 5,680 - 13,632

Full time

14 days+
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Job summary

An established industry player is seeking a skilled Associate Medical Data Review Manager to oversee data quality and integrity in clinical studies. This role involves reviewing patient-reported data, conducting trend analysis, and ensuring compliance with protocols. The ideal candidate will possess a strong medical background, excellent project management skills, and the ability to work collaboratively in a dynamic environment. Join a forward-thinking organization dedicated to improving healthcare outcomes through data excellence and innovation. If you have a passion for clinical data and the drive to make a difference, this opportunity is perfect for you.

Qualifications

  • 2+ years of experience in clinical data review and project management.
  • Strong understanding of medical data and ability to identify issues.

Responsibilities

  • Review patient data for anomalies and ensure data quality.
  • Provide project management support and drive data integrity.

Skills

Clinical Data Understanding
Medical Terminology
Pharmacology Knowledge
Attention to Detail
Interpersonal Skills
Analytical Skills
Project Management
Communication Skills

Education

MBBS or MD

Job description

Job Title / Primary Skill: Associate Medical Data Review Manager

Years of Experience: 2 + Years.

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.
  • 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).
  • Serve as POC/ Back-up POC.
  • 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.

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.
  • Attention to detail.
  • Interpersonal and analytical skills.
  • 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.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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.

PHYSICAL REQUIREMENTS:

  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Regular sitting for extended periods of time.

Seniority level: Mid-Senior level

Employment type: Full-time

Job function: Research

Industries: Research Services

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