Clinical Trial Manager

Job Title: Clinical Trial Manager

Job Location: Slovakia

Job Location Type: On-site

Job Contract Type: Permanent

Job Seniority Level: Mid-Senior level

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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