Clinical Research Associate (Germany, Home-based) - IQVIA Biotech (W/M/D) (R1068188) in Munich, DE at IQVIA™

发布日期: 10/1/2019

职位快速浏览

  • 员工类型:
    Full-Time
  • 地点:
    Munich, DE
  • 经验:
    Not Specified
  • 发布日期:
    10/1/2019
  • Job ID:
    R1068188

职位描述

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.

IQVIA Biotech, A Iqiva Company, is a global full service CRO, committed to providing an outstanding service to our clients as well as our employees. We focus on providing excellent training and career development opportunities, encouraging growth from within our talented workforce.

We have a vacancy within our Clinical Monitoring Team for an experienced permanent Clinical Research Associate to join our team in Germany

This is a great opportunity for a CRA to join a progressive and developing CRO. Being an integral part to the clinical monitoring team. Making an impact in the Oncology, Medical Devices and Dermatology markets, You’ll have training and development to plan and progress your career in the direction you choose. IQVIA Biotech offers a dynamic and fast paced environment that allows you not only to utilize your current skill set and experience as well as to develop further.

Requirements and Responsibilities:

  • You will be responsible for ensuring that, at the site level, the Clinical Monitoring Plan is implemented.
  • To ensure appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework.
  • Excellent knowledge of Good Clinical Practice (GCP) and also good working knowledge of conducting clinical trials in general.
  • Experience of performing site start up procedures, routine monitoring and site closure.
  • Excellent interpersonal and organisational skills
  • Ability to manage multiple priorities across various clinical trials
  • Ability to travel.

We have a vacancy within our Clinical Monitoring Team for an experienced permanent Clinical Research Associate to join our team in Germany

This is a great opportunity for a CRA to join a progressive and developing CRO. Being an integral part to the clinical monitoring team. Making an impact in the Oncology, Medical Devices and Dermatology markets, You’ll have training and development to plan and progress your career in the direction you choose. IQVIA Biotech offers a dynamic and fast paced environment that allows you not only to utilize your current skill set and experience as well as to develop further.

Requirements and Responsibilities:

  • You will be responsible for ensuring that, at the site level, the Clinical Monitoring Plan is implemented.
  • To ensure appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework.
  • Excellent knowledge of Good Clinical Practice (GCP) and also good working knowledge of conducting clinical trials in general.
  • Experience of performing site start up procedures, routine monitoring and site closure.
  • Excellent interpersonal and organisational skills
  • Ability to manage multiple priorities across various clinical trials
  • Ability to travel

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.



Job ID: R1068188

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