Clinical Trial Physician

What We OfferJoining our consulting team in Belgium means giving your career a step forward. Thanks to the privileged partnership we have with our well-established clients, leaders in their domain, we offer our consultants unique projects to develop their skills, and put their professional experience in the pharma industry on the fast track. As an expert on the client side, you can count on us to support you at each step of your project thanks to regular touch points with our Key Account Manager. We then also carefully choose with you what would be your next assignment that is matching your career goal whether it is in Consulting or in one of our Functional Services Platforms. We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience. About the RoleWe are looking for an experienced Clinical Trial Physician to join an unblinded/restricted study team. The ideal candidate will have a strong background in clinical research, medical monitoring, and safety data review, with the ability to work closely with investigators, site staff, and CRAs in a global clinical trial environment. Key Responsibilities• Clinical review of study data• Medical monitoring activities• Oversight of potentially unblinding data and related processes• Participation in restricted/unblinded study team discussions• Support the overall safety and integrity of the clinical trial Main Activities• Monitor lymphocyte data• Monitor cardiac data related to Day 1 dosing and treatment re-initiation• Review and monitor pharmacodynamic (PD) data• Participate in monthly unblinded/restricted team meetings• Prepare monthly Clinical Monitoring Reports• Review potentially unblinding query responses within the main EDC system• Communicate directly with investigators, site staff, and CRAs regarding lymphocyte and cardiac monitoring findings and any potentially unblinding data Required Qualifications• MD (Medical Doctor) degree — mandatory• Proven experience as a Clinical Trial Physician, Medical Monitor, or similar role within clinical research• Strong understanding of clinical trial conduct, data review, and medical monitoring• Experience working with EDC systems• Fluent English, both written and spoken• Ability to work independently in a remote and international environment Our BenefitsJoining Astek means choosing:• an experience accelerator, where every assignment is an opportunity to progress• access to a multitude of technically exciting projects for our clients as well as internally• individualized, local support for a tailored career path• continuous learning, thanks to our internal training academy• a friendly and inclusive work environment, supported by #TopEmployer2026 certified HR practices Let's move forward.Alsinova — An Astek Company