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Clinical Trial Manager

  1. Slovakia
2025-120119
  1. ICON Strategic Solutions
  2. Clinical Trial Management
  3. Home-Based

About the role

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

CTM (Local Trial Manager) would be a primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up  to close out at a country level in accordance with ICH-GCP and other applicable local regulation and will maintain 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 relationship
  • 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.

Job Function:

  • Planning, management, and oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team 
  • Supports country-level operational planning and accountable for site selection within assigned country/-ies.
  • Contributes and develops to program/study-specific materials – e.g., monitoring plan, study specific training documents.
  • Supports and contributes to Clinical Study Teams / Trial Management Teams as applicable, agenda driven, present at meetings.
  • Communicates country status (including timelines and deliverables) to key stakeholders (e.g., Global Clinical Managers , Program Managers, CST or TMT, Development Operations Manager , etc) with oversight as required and ensures updates to relevant system
  • Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country/-ies.
  • Contributes to, deliver and/or lead CRA, Investigator and Study Coordinator training
  • Provides oversight and monitoring of applicable vendor activities e.g., laboratories and equipment provisionin
  • Engages with local cluster team and local functions from a study perspective

#LI-NR1

# LI- Remote


- Local knowledge and expertise of regulatory environment, study start up process and associated timelines etc

- Slovak and English fluent

- Previous Clinical Trial Management experience required 

- BA/BS/BSc or Master's degree in scientific field preferred 

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