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IQVIA

Runs drug trials and sells health data to pharma

HTA Analyst - AMNOG

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A Master’s degree or PhD in life sciences, biostatistics, epidemiology, pharmacy, or a related field.
  • Initial experience in HTA, AMNOG, HEOR, or Market Access in industry, consultancy, or a research institute is sought.
  • A solid understanding of clinical study designs, endpoints, and statistical principles is required.
  • Experience in scientific and medical writing is required.
  • Fluency in German and English, written and spoken, is an absolute must.
  • Strong analytical skills and attention to detail are required.
  • Ability to translate complex data into clear, structured, and persuasive text is required.
  • A structured, reliable, and quality-driven working style is required.
  • Strong teamwork and communication skills are required.
  • Strategic and critical thinking focused on quality, service, and solutions is required.
  • Ability to work independently and stay well organized is required.
  • Strong customer orientation, confident presentation skills, responsibility, reliability, and communication skills are required.
  • High attention to detail and an audit-ready mindset are required.

Responsibilities

  • Contribute to developing German AMNOG dossiers, focusing on Modules 2–4.
  • Assess clinical trial data scientifically, including efficacy, safety, patient-relevant endpoints, and subgroup analyses.
  • Conduct systematic literature reviews and structured evidence syntheses.
  • Write AMNOG dossier texts and updates, written statements and responses for G-BA procedures and hearings, scientific reports, slide decks, and selected publications.
  • Support indirect treatment comparisons and interpret statistical outputs.
  • Collaborate with Market Access, HEOR, Medical Affairs, and the EU-HTA team.
  • Ensure scientific quality, clarity, and consistency of HTA-related documents.
  • Monitor and interpret methodological developments from IQWiG, G-BA, and relevant HTA bodies.

Desired Qualifications

  • Familiarity with the German AMNOG process, IQWiG methodology, or G-BA procedures is an advantage.
  • Affinity for data and strong analytical and conceptual skills; advanced Excel skills; familiarity with Python or another programming language.
  • A strong background in statistics, data sciences, or programming.
  • Proficiency in MS Office and experience with reference management tools.
  • More than two years of experience in advanced SAS and R programming.
  • More than two years of hands-on clinical data analysis experience with CDISC SDTM/ADaM datasets.
  • A solid understanding of core statistical methods used in clinical trials and HEOR.

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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