Our client, a growing and innovative organization in the pharmaceutical/biotechnology sector, is seeking an experienced Clinical Trial Director to lead and oversee global clinical development programs. This role will be based on-site in Antwerp, where the successful candidate will take strategic and operational responsibility for the planning, execution, and delivery of clinical trials.
The Clinical Trial Director will collaborate cross-functionally with clinical operations, regulatory, medical, data management, and external partners to ensure studies are delivered on time, within budget, and in compliance with regulatory and quality standards.
Key Responsibilities
Provide strategic leadership and oversight for the design, planning, and execution of clinical trials across multiple phases (Phase I–III).
Lead cross-functional study teams and coordinate activities across clinical operations, regulatory affairs, pharmacovigilance, and data management.
Develop and implement clinical development plans, trial protocols, and study timelines.
Ensure all clinical trials are conducted in compliance with ICH-GCP, regulatory requirements, and company SOPs.
Manage relationships with CROs, vendors, and clinical sites to ensure effective study delivery.
Monitor study progress, budgets, and key milestones; identify risks and implement mitigation strategies.
Contribute to regulatory submissions and interactions with health authorities where required.
Oversee data integrity and ensure quality standards are maintained throughout the clinical trial lifecycle.
Present clinical progress updates to senior leadership and key stakeholders.
Support the preparation of clinical study reports, publications, and scientific communications.
Requirements
Advanced degree in Life Sciences, Medicine, Pharmacy, or a related field (PhD, PharmD, or MD preferred).
10+ years of experience in clinical research, with significant leadership responsibility in clinical trial management.
Proven experience managing global clinical trials within the pharmaceutical, biotech, or CRO industry.
Strong knowledge of ICH-GCP guidelines and regulatory frameworks.
Demonstrated ability to lead cross-functional teams and complex clinical programs.
Experience working with external vendors and CROs.
Excellent project management, leadership, and communication skills.
Fluency in English; additional European languages are an advantage.
Willingness to work on-site in Antwerp.
What Our Client Offers
Opportunity to play a key leadership role in advancing innovative therapies.
A collaborative and scientifically driven environment.
Competitive salary and benefits package.
Career growth within a fast-evolving clinical development organization.
How to Apply
If you are interested in learning more about this opportunity, please submit your CV or contact us confidentially for further details.
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