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IQVIA

Runs drug trials and sells health data to pharma

Assoc Medical Data Review Mgr

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • A five-year college degree or MBBS is required for the “Other Medic” qualification.
  • A bachelor's degree in a clinical or biological area and three years of work experience in clinical practice or a clinical research-related field are required; equivalent education, skills, and experience may substitute for the degree.
  • Experience in clinical data sciences at a contract research organization, pharmaceutical company, or other medical environment, with demonstrated leadership experience, is required.
  • A good understanding of clinical and medical data is required.
  • Knowledge of medical terminology, pharmacology, anatomy, and physiology is required.
  • A medical background and an operational focus on metrics and status information to take appropriate actions to resolve issues are required.
  • Excellent communication, interpersonal, customer service, and teamwork skills are required.
  • Excellent organizational and problem-solving skills are required.
  • Project management and coaching skills are required.
  • Ability to work with minimal supervision using available resources is required.
  • Ability to work on multiple projects and manage competing priorities is required.
  • Strong customer focus and ability to establish and maintain effective working relationships with coworkers, managers, and clients are required.

Responsibilities

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

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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