About the Role
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.