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Associate Site Manager with German Language

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Primary Location: Budapest, Hungary Additonal Locations: Athens, Greece,GRC; Bratislava, Slovakia,SVK; Bucharest, Romania,ROU; Oeiras, Portugal,PRT; Sofia, Bulgaria,BGR; Warsaw, Poland,POL; Zagreb, Croatia,HRV Full time R1307481

Job description

Associate Site Manager

Real-World Evidence

Hybrid: EMEA

Join us on our exciting journey!

IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.

Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.

We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.

Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.

Job Overview:

As an Associate Site Manager, you will act as the first line of escalation for site management questions and issues for the assigned projects.

You will apply clinical research experience and skills to engage site management/monitoring staff to ensure process and practice methodology is applied consistently and in accordance with project scope and budget, SOPs, policies, good clinical practices and applicable regulatory requirements.

You will also assist with the development of Site Recruitment, SPS Operations and SPS Risk Management Plans.

You will have the opportunity to collaborate with other functional groups within the company such as data management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.

Requirements:

  • Bachelor's degree in a health care or other scientific discipline.
  • 3 years of monitoring experience, team leadership experience; or equivalent combination of education, training and experience
  • In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Strong written and verbal communication skills including good command of English and German language (C1 level).

What is in it for you?

  • Global exposure
  • Variety of therapeutic areas
  • Collaborative and supportive team environment
  • Access to cutting-edge in-house technology
  • Excellent career development and progression opportunities
  • Work-Life Balance

JOIN US

  • Embrace your curiosity and grow your career in an exciting environment where development is a priority.
  • Think boldly and disrupt conventional thinking.
  • Enjoy what you do.

Whatever your career goals, we are here to ensure you get there!

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

Apply now

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