Clinical Trial Manager
- Slovakia
- ICON Strategic Solutions
- Clinical Trial Management
- Home-Based
TA Business Partner
- Icon Strategic Solutions
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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