Manager, Trial Delivery Management

Jobtailor

Beerse

Sur place

EUR 90 000 - 130 000

Plein temps

Il y a 3 jours

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Résumé du poste

Jobtailor in Belgium seeks an accomplished Clinical Trial Manager to lead study-level activities, vendor oversight, and risk management across phases I–IV.

You will set up trial documents, manage budgets, coordinate country/regional activities, and mentor the team while driving process improvements and ensuring inspection readiness.

Qualifications

BS degree or equivalent, with preferred areas of study including Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
Minimum of 8 years in Pharmaceutical, Healthcare or related industries
Experience in and knowledge of the pharmaceutical development process
Clinical research operational knowledge and experience across multiple study phases (Phase I-IV)
Ability to manage all aspects of clinical trial execution
2-3 years’ experience leading multiple aspects of a global clinical trial
Excellent leadership skills and proven ability to foster team productivity and cohesiveness
Experience leading without authority in multifunctional, matrixed, and global environments
Excellent decision-making, analytical, and financial management skills
Ability to operate and execute with limited supervision
Experience mentoring/coaching others
Strong project planning/management, communication, and presentation skills
Willingness to travel up to 15-20% of the time
Preferred related industry experience: Pharmaceutical, Biopharmaceutical, Biotechnology

Responsabilités

Execute study-level activities
Create and update critical trial-specific documents, including Monitoring Guidelines, Informed Consent Forms, and Investigational Medicinal Product documentation
Set up and manage day-to-day study vendor activities, including statement-of-work creation and budget oversight
Coordinate and oversee country/regional trial management activities
Align feasibility strategy with local teams
Perform country-level risk reviews and monitor projects conducted across countries
Support development of program-level compound training in collaboration with Clinical and CTL&D Medical Writing
Provide input into trial-level operational strategies
Resolve trial-related issues and mitigate trial-related risks
Participate in process improvement activities at trial, compound, and cross-DU levels
Support Health Authority inspections and identify program-level risks and mitigation plans
Mentor and support onboarding of new Trial Management team members
Foster employee engagement, inclusion, and Credo Behaviors

Connaissances

Clinical Trial Execution

Leadership

Project Planning/Management

Risk Management

Decision-Making

Analytical Skills

Communication Skills

Presentation Skills

Formation

Bachelor’s degree or equivalent in Life Sciences

Description du poste

Execute study-level activities
Create and update critical trial-specific documents, including Monitoring Guidelines, Informed Consent Forms, and Investigational Medicinal Product documentation
Set up and manage day-to-day study vendor activities, including statement-of-work creation and budget oversight
Coordinate and oversee country/regional trial management activities
Align feasibility strategy with local teams
Perform country-level risk reviews and monitor projects conducted across countries
Support development of program-level compound training in collaboration with Clinical and CTL&D Medical Writing
Provide input into trial-level operational strategies
Resolve trial-related issues and mitigate trial-related risks
Participate in process improvement activities at trial, compound, and cross-DU levels
Support Health Authority inspections and identify program-level risks and mitigation plans
Mentor and support onboarding of new Trial Management team members
Foster employee engagement, inclusion, and Credo Behaviors

Requirements

BS degree or equivalent, with preferred areas of study including Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
Minimum of 8 years in Pharmaceutical, Healthcare or related industries
Experience in and knowledge of the pharmaceutical development process
Clinical research operational knowledge and experience across multiple study phases (Phase I-IV)
Ability to manage all aspects of clinical trial execution
2-3 years’ experience leading multiple aspects of a global clinical trial
Excellent leadership skills and proven ability to foster team productivity and cohesiveness
Experience leading without authority in multifunctional, matrixed, and global environments
Excellent decision-making, analytical, and financial management skills
Ability to operate and execute with limited supervision
Experience mentoring/coaching others
Strong project planning/management, communication, and presentation skills
Willingness to travel up to 15-20% of the time
Preferred related industry experience: Pharmaceutical, Biopharmaceutical, Biotechnology

Core Competencies

Demonstrates expertise in clinical trial execution, including managing study-level activities, vendor oversight, and risk management across multiple phases. Proven ability to lead teams, mentor staff, and support operational strategies in the pharmaceutical and healthcare sectors.

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