Job Description
Join Our Team as a Medical Monitor in Dermatology & Rheumatology - Remote in Poland or Spain.
Are you a seasoned medical professional passionate about advancing clinical research in dermatology and rheumatology? We are seeking a dedicated Medical Monitor to join a dynamic, innovative organization that values expertise, collaboration, and patient safety. This full‑time, remote role offers the flexibility to work from Poland or Spain and provides an exciting opportunity to influence clinical development programs across Europe, ensuring the highest standards of safety and scientific integrity.
What You’ll Bring:
* A medical degree, with dermatology residency training considered an asset
* At least 5 years of hands‑on experience in clinical research within CRO, pharmaceutical, or biopharmaceutical environments
* Minimum of 3 years serving as a Medical Monitor, Medical Reviewer, or Drug Safety Physician for clinical trials
* Deep understanding of the drug development process, clinical safety practices, and regulatory guidelines
* Exceptional communication skills, with the ability to build positive relationships with investigators, site staff, and internal teams
* Strong organizational skills to manage multiple projects efficiently and effectively
Nice to Have:
* Experience working specifically within dermatology and rheumatology therapeutic areas
* Familiarity with pharmacovigilance procedures and safety committee operations
* Fluency in additional European languages and advanced data analysis skills
Preferred Education and Experience:
* Medical degree with relevant residency training
* Proven track record in clinical safety and medical monitoring roles in international trials
* Past involvement in protocol development, safety reporting, and regulatory compliance
Additional Requirements:
* Ability to participate in on‑call safety support outside regular business hours
* Willingness to engage in a flexible, home‑based work environment
* Commitment to ongoing professional development and collaborative teamwork
If you are ready to make a meaningful impact in clinical research and thrive in a collaborative and innovative setting, we encourage you to apply now. Step into a role that combines your expertise with the opportunity for professional growth and genuine contribution to medical science.
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert
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