1 day ago Be among the first 25 applicants
Direct message the job poster from Panda International
Partner & Manager @ Panda International | Recruitment Advisor | Biopharma and Medtech
An international biopharmaceutical company is seeking an experienced Interim Senior Medical Director to provide medical leadership and oversight across clinical trials from Phase I to Phase III, with a focus on data integrity, patient safety, and regulatory compliance. Based in Europe, this strategic and hands-on role is ideal for a senior physician with deep experience in clinical research, preferably within immunology or SLE.
* Start Date: ASAP
* Contract Duration: 6 months
* Commitment: Full-time preferred
* Interview Process: Streamlined for quick onboarding
Responsibilities
* Clinical Study Leadership – Act as the medical representative of the Clinical Study Team (CST), overseeing all medical aspects of clinical trials.
* Medical Oversight – Monitor patient safety and data integrity, following ICH-GCP and internal standards as outlined in the Medical Monitoring and Oversight Plan.
* Medical Review & Input –
* Review patient data, CRFs, data listings, and study documents (protocols, SAPs, ICFs, IBs, IMPDs).
* Provide medical input on CRO/vendor selection, and work closely with CROs and key opinion leaders.
* Training & Support – Provide training to investigators, CRAs, and vendors, and act as a central point of contact for medical study-related questions.
* Risk Management & CAPA – Participate in the Safety Management Team, assess and mitigate safety risks, and contribute to CAPA development and protocol deviation management.
* Regulatory Contributions – Support regulatory submissions and external communication of results, including CSR review and publications.
Requirements
* MD or MD/PhD with at least 10 years’ experience in clinical research within the pharmaceutical industry.
* Minimum 3 years of medical practice experience; strong foundation in clinical medicine.
* Solid understanding of Phase II–III drug development, preferably in Immunology or SLE.
* Demonstrated leadership in matrixed clinical development teams.
* High-level strategic thinking and analytical capabilities.
* Experience collaborating with regulatory authorities, CROs, and internal R&D functions.
* Excellent scientific writing, communication, and presentation skills.
* Fluent/native-level English (spoken and written).
Why This Role?
* Leadership in High-Impact Trials – Guide the clinical strategy and execution of pivotal trials across therapeutic areas.
* Regulatory Influence – Shape key documents for regulatory submissions and external scientific communication.
* Strategic & Operational Blend – Combine high-level medical strategy with detailed trial oversight.
* Collaborative Environment – Work with cross-functional teams and top-tier CROs and KOLs.
Interview Process
* 1st Interview – With Clinical Development Leadership
* 2nd Interview – With Medical Affairs, Regulatory, or Program Team
* Start Date: ASAP
Seniority level
* Seniority level
Director
Employment type
* Employment type
Temporary
Job function
* Job function
Science and Product Management
Referrals increase your chances of interviewing at Panda International by 2x
Get notified about new Director Medical Affairs jobs in Mechelen, Flemish Region, Belgium.
Medical Director, Oncology Diagnostics - Europe
Antwerp, Flemish Region, Belgium 2 days ago
Brussels, Brussels Region, Belgium 1 month ago
Senior Director of Medical Strategy (Endocrinology)
Antwerp, Flemish Region, Belgium 1 day ago
Global Medical Director Gastroenterology Specialty Care
Brussels, Brussels Region, Belgium 2 weeks ago
Sr. Medical Director - Mechelen (BE), Consultant (6 months contract)
Mechelen, Flemish Region, Belgium 3 days ago
Medical Director - Oncology/Cardiology/Gastroenterology/Endocrinology/Radiology/Infectious Disease/Immunology/Nephrology/Psychiatrist
(Senior) Medical Director - Rheumatology (Client - dedicated), EMEA
Brussels, Brussels Region, Belgium 1 week ago
Biostatistics Director (m/f/x) for Evidence Generation
Antwerp, Flemish Region, Belgium 3 days ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr