PRAHS

Clinical Trial Manager

Job Locations (All)-- | AR
Posted Date 5 months ago(6/28/2024 4:50 PM)
ID
2024-111424

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Responsibilities

What will you be doing?

 

  • Primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out at a country level in accordance with ICH-GCP and other applicable local regulations.
  • Maintains the quality and scientific integrity of clinical trials at a country level.
  • Collaborates with cross functional internal and external stakeholders to ensure timely execution, budget execution of clinical trial deliverables within the country.
  • Maintains expert country, site and protocol knowledge to support sites with questions as well as build strong site relationships.
  • Partners with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery.
  • Accountable for study deliverables and drives key decisions within set country.

 

Qualifications

What You Need to Have:

 

  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse); or equivalent work experience, required.
  • Minimum 2-3 years’ experience of leading local/regional or global teams
  • Minimum 2-3 years’ clinical trial project management experience
  • Advanced knowledge of global clinical trial management
  • Fluency in local language and business English


Benefits of Working in ICON:

 

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

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