Our client operates within the global pharmaceutical industry and focuses on clinical research and the development of innovative therapies. Working in a highly regulated and collaborative environment, the organization supports clinical studies that contribute to advancing healthcare. To strengthen the Clinical Study team, our client is seeking a Medical Advisor who can bridge science, operations, and stakeholders.
Job Description
As a Medical Advisor, you act as the medical and scientific expert within clinical trial activities. You support both local and international study teams by ensuring that research is conducted in line with regulatory standards and scientific best practices. The role involves advising on study designs, supporting feasibility assessments, and addressing medical questions that arise during trials. You collaborate with internal departments and external partners such as investigators and specialists, ensuring strong alignment between global strategies and local execution. You also contribute to documentation and support communication with regulatory authorities.
Responsibilities
- Provide medical and scientific guidance to clinical study teams.
- Support study design, feasibility, and patient recruitment strategies.
- Act as a key contact for investigators, clinical sites, and internal stakeholders.
- Engage with external experts and Key Opinion Leaders to exchange insights.
- Deliver medical training and knowledge sharing to project teams.
- Contribute to clinical documentation and regulatory submissions.
- Respond to medical and scientific questions from authorities or affiliates.
- Ensure patient safety and data integrity throughout clinical activities.
Requirements
- Medical degree preferred, or PhD/PharmD in life sciences.
- Strong scientific knowledge and understanding of clinical development.
- Experience in clinical practice, research, or pharmaceutical development.
- Familiarity with ICH-GCP guidelines and regulatory frameworks.
- Strong stakeholder management and communication skills.
- Fluent in English.
- Proactive, independent, and comfortable working in a dynamic environment.
- Work visa required, and already situated in the Netherlands. If these requirements are not met you will not receive a response to your application
Benefits
- Temporary contract (approx. 8 months) to cover a leave period.
- Minimum of 32 working hours per week.
- Flexible and hybrid working environment.
- Competitive salary between 70-90K, depending on experience.
- Opportunity to work in an international and multidisciplinary setting.
- Exposure to complex clinical research projects and professional growth.
- Location: Amsterdam Area
- Vacancy number: 27282
