FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
About the role
Key responsibilities & impact- Provide accurate, timely, and compliant medical information to internal stakeholders, field teams, and external inquiries from healthcare professionals.
- Serve as a scientific resource for product data, literature, and device-related information related to injectables used in aesthetic procedures.
- Support development and execution of medical education programs, speaker training, case-based discussions, and non-promotional educational activities.
- Support to identify, engage, and maintain relationships with key opinion leaders (KOLs) and regional experts in aesthetic medicine, dermatology, and related fields; assist with KOL mapping and management plans.
- Support local observational studies, registries, post-marketing commitments, and real-world evidence initiatives under supervision.
- Assist in the preparation of scientific communications, posters, abstracts, white papers, and regulatory-required documentation.
- Ensure Medical Affairs activities comply with regional regulations, industry codes (e.g., EFPIA/ABPI equivalents in region), and company policies.
- Partner with Clinical Development, Regulatory, Marketing, Sales, Pharmacovigilance, and Medical Information to implement regional medical strategies.
- Monitor relevant scientific literature, guidelines, and competitor activity to inform medical strategy and respond to inquiries.
- Maintain accurate records of medical activities, meetings, and approved materials in regional systems according to policy.
Requirements
What you’ll need- Medical Degree or Master degree in a scientific discipline or higher
- 1-3 years in Medical Affairs, Medical Information, or related field within the pharmaceutical/medical device industry.
- Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and in medical research in general.
- Knowledge of the scientific methods applied to clinical research and the current legislative/regulatory controls.
- Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.
- Ability to handle complex medical and scientific information confidently, and to prepare content in a clear, structured and easily understandable way.
- Analytical mindset, strong problem-solving skills and a proactive, self-directed and reliable way of working.
- Comfortable using digital communication channels and modern collaboration tools, with the ability to work confidently across different formats and systems.
- Team player with empathy, adaptability and drive, contributing to a collaborative working environment and shared results.
- Excellent English
Benefits
Comp & perks- Medical Information and Scientific Support
- Medical Education and KOL Engagement
- Evidence Generation and Lifecycle Management
- Regulatory and Compliance Support
- Cross-Functional Collaboration
- Literature Surveillance and Competitive Intelligence
- Documentation and Record Keeping
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical informationscientific communicationclinical researchregulatory compliancemedical educationdata analysisliterature reviewinjectablesaesthetic medicinescientific methods
Soft Skills
problem-solvinganalytical mindsetcommunicationteam playeradaptabilityempathyself-directedreliableproactivecommitment to quality
Certifications
Medical DegreeMaster's degree in scientific discipline