Lead, Trial Delivery Management

Jobtailor; Breda; On-site; EUR 70,000 - 100,000; Full time

Job summary

Jobtailor in Breda, Netherlands is seeking an experienced Clinical Trial Manager to lead study-level activities, oversee document governance, and manage vendor relationships across global trials.

You will drive feasibility alignment with local teams, perform country-level risk reviews, support regulatory inspections, and mentor new team members while collaborating with Clinical, CTL&D, and Medical Writing to shape program-level strategies.

Qualifications

• BS degree in Life Sciences or equivalent.
• Minimum of 4 years clinical trial experience.
• Experience across multiple phases I-IV and regulatory compliance.

Responsibilities

• Execute study-level activities
• Create and update critical trial-specific documents, including Monitoring Guidelines, Informed Consent Forms, and IMP-related documentation
• Manage vendor setup and day-to-day study vendor activities, including SOW creation and budget oversight
• Coordinate and oversee country/regional trial management activities
• Align feasibility strategy with local teams and perform country-level risk reviews
• Support development of program-level compound training in collaboration with Clinical, CTL&D, and 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 team members, particularly in Trial Management

Skills

Clinical Trial Management

Clinical Research Regulations

Project Planning/Management

Leadership Skills

Risk Management

Education

Bachelor's degree in Life Sciences

Tools

CTMS

Job description

• Execute study-level activities
• Create and update critical trial-specific documents, including Monitoring Guidelines, Informed Consent Forms, and IMP-related documentation
• Manage vendor setup and day-to-day study vendor activities, including SOW creation and budget oversight
• Coordinate and oversee country/regional trial management activities
• Align feasibility strategy with local teams and perform country-level risk reviews
• Support development of program-level compound training in collaboration with Clinical, CTL&D, and 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 team members, particularly in Trial Management

Requirements

• BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
• Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industries
• Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV)
• Ability to manage multiple aspects of execution of a clinical trial
• 2-3 years’ experience supporting multiple aspects of a global clinical trial
• Excellent leadership skills and proven ability to foster team productivity and cohesiveness
• Experience leading without authority and 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 industry experience: Pharmaceutical, Biopharmaceutical, Biotechnology
• Preferred skills include Clinical Research and Regulations, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Clinical Trials, Laboratory Operations, Project Integration Management, Quality Assurance (QA), Regulatory Compliance, Research and Development, Research Ethics, and Standard Operating Procedures (SOP)

Core Competencies

Demonstrates expertise in clinical trial management, including the creation of trial-specific documents and vendor oversight, while effectively leading teams and managing multiple aspects of trial execution. Proficient in clinical research regulations and quality assurance practices, with a strong focus on risk management and process improvement.

Highest-signal resume keywords

• Clinical Trial Management
• Clinical Research Regulations
• Project Planning/Management
• Leadership Skills
• Risk Management

Hard Skills

• Clinical Trial Designs
• Clinical Trial Management Systems (CTMS)
• Monitoring Guidelines
• Informed Consent Forms
• Budget Oversight
• Laboratory Operations
• Quality Assurance (QA)
• Regulatory Compliance
• Research Ethics
• Standard Operating Procedures (SOP)

Soft Skills

• Excellent Decision-Making
• Analytical Skills
• Communication Skills
• Presentation Skills
• Mentoring/Coaching

Industry Keywords

• Pharmaceutical
• Biopharmaceutical
• Biotechnology
• Healthcare
• Clinical Research