Junior Analyst or Consultant mwd - Health Technology Assessment HTA - German Native Speaker Spa[...]

Es52; Madrid; A distancia; EUR 38.000 - 60.000; Jornada completa

Descripción de la vacante

A leading healthcare company is seeking a medical writer in Madrid to design clinical trial training tools. You will be responsible for preparing HTA dossiers and interpreting clinical data. The ideal candidate must be proficient in German and possess a Master's degree in a relevant field. Join a multicultural team to make a meaningful impact on healthcare.

Formación

• Advanced proficiency in German language.
• Familiar with qualitative and quantitative research studies.
• Ability to identify deficiencies in deliverables.

Responsabilidades

• Describe indications and therapeutic needs for HTA dossiers.
• Calculate annual therapy costs for HTA dossiers.
• Interpret clinical study data from Clinical Study Reports.

Conocimientos

Attention to detail

Proficiency in proofreading and editing in English

Understanding of statistical methods

Ability to manage multiple tasks

Educación

Master's degree or equivalent in psychology, epidemiology, medicine, or related fields

Herramientas

Microsoft Office

Descripción del empleo

IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

We are seeking medical writers to join our team in designing immersive & engaging clinical trial training tools and experiences.

If you want to play a key role in a multicultural, dynamic, and committed team, this could be the role for you!

Medical writing responsibilities include:

1. Describing indications, target patient populations, and therapeutic needs as part of an HTA dossier.
2. Calculating annual therapy costs as part of an HTA (AMNOG) dossier.
3. Understanding clinical evidence on new compounds and assessing study quality (using CONSORT) and bias potential as part of an HTA dossier.
4. Interpreting clinical study data from Clinical Study Reports.

Qualifications and skills required:

• Advanced proficiency in German language.
• Proficient in proofreading and editing in English.
• A minimum of a Master's degree or equivalent in psychology, epidemiology, educational psychology, outcomes research, sociology, medicine, medical science, or related fields.
• Careful attention to detail and accuracy.
• Computer literacy with knowledge of Microsoft Office applications.
• Ability to work in a fast-paced environment, managing multiple tasks effectively.
• Good understanding of statistical methods used in clinical trials and interpretation of their results.
• Familiarity with qualitative and quantitative research studies for clinical outcome assessments.
• Ability to identify deficiencies, errors, and inconsistencies in deliverables.

Additional information:

• IQVIA is recognized as a top employer and industry leader, with numerous awards and recognitions.
• IQVIA is an equal opportunity employer committed to diversity and inclusion.
• Join us to help reimagine healthcare and make a meaningful impact worldwide.

Experience and employment details:

Key Skills: Business Development, IT Sales, Insurance Management, LAMP, Com+ Dcom

Employment Type: Full-Time

Experience: [Specify years of experience]

Vacancy: 1