Clinical Research Specialist
SkinVision
Amsterdam, Netherlands
Posted on Jun 5, 2025
About SkinVision:
SkinVision is a pioneering AI scale-up on a mission to save 250,000 lives in the next decade by transforming early skin cancer detection. Our flagship mobile app uses advanced AI to assess skin lesions and connect users efficiently with the healthcare system. With over a million users and 30,000 new users every month, we are rapidly scaling our impact. Join our purpose-driven, international team at the forefront of innovation in dermatology.
Position overview:
As the Clinical Research Specialist, you will be responsible for the management of clinical studies focused on the performance, safety, and efficacy of our products. You will work within an international team to deliver high-quality clinical research in compliance with regulatory requirements and internal standards.
Key Responsibilities:
Research shows that while men apply to jobs when they meet an average of 60% of the criteria, women tend to only apply when they check every box. If you feel energized by our mission and would like to use your first-class talent to accelerate the growth of SkinVision, but don't necessarily meet every single point on the job description, please still apply. We'd love to receive your application and see if you could be a good fit.
SkinVision is a pioneering AI scale-up on a mission to save 250,000 lives in the next decade by transforming early skin cancer detection. Our flagship mobile app uses advanced AI to assess skin lesions and connect users efficiently with the healthcare system. With over a million users and 30,000 new users every month, we are rapidly scaling our impact. Join our purpose-driven, international team at the forefront of innovation in dermatology.
Position overview:
As the Clinical Research Specialist, you will be responsible for the management of clinical studies focused on the performance, safety, and efficacy of our products. You will work within an international team to deliver high-quality clinical research in compliance with regulatory requirements and internal standards.
Key Responsibilities:
- Design, plan, and manage investigator-initiated and sponsored clinical research projects in line with company strategy and regulatory timelines.
- Develop and maintain effective collaborations with internal stakeholders and external partners (e.g., dermatologists, researchers, KOLs).
- Collaborate on protocol development and study design for dermatology-related clinical trials.
- Support strategic discussions with B2B partners to ensure clinical evidence aligns with product goals.
- Train and support clinical study teams, physicians, and cross-functional partners to ensure data integrity and compliance.
- Prepare study materials, training content, and maintain essential study documentation.
- Develop and negotiate study budgets and contracts with investigators and CROs.
- Manage database activities, site training, and investigator meetings.
- Oversee relationships with CROs, study sites, and vendors to ensure successful trial execution.
- Attend relevant scientific conferences to stay updated on dermatology and clinical trends.
- Ensure compliance with internal standard operating procedures (SOPs), ICH-GCP, ISO 14155, and applicable regulatory standards.
- Contribute to medical writing, publications, and dissemination of clinical findings.
- Work closely with regulatory, quality assurance, product & technology, and marketing teams to align clinical research operations with business needs.
- Bachelor’s or master’s degree in relevant biomedical, clinical, and technical sciences.
- 3-5 years of experience in clinical research or a related field, preferably in healthcare or medical devices.
- Solid understanding of clinical trial processes, including EU MDR, ISO 14155, and ICH-GCP.
- Experience in medical writing and scientific publication.
- Project management and organizational skills.
- Advanced analytical, problem-solving abilities, and communication skills.
- Proven ability to build and maintain relationships with KOLs, doctors, and researchers.
- Willingness to travel as required.
- Fluency in English; proficiency with Microsoft Office and Google Workspace.
- Experience in the medical device industry (preferably SaMD) and/or dermatology.
- Familiarity with EC/CA submissions and regulatory documentation.
- Knowledge of health economics; healthcare systems, market, and patient workflows.
- Experience with database management and clinical data software.
- Fluency in Dutch or other languages is a plus.
- A competitive salary based on your experience, a bonus structure, and additional benefits (e.g., travel reimbursement and training budget).
- Hybrid work setup: 3 office days with a healthy lunch and 2 days remote.
- Company laptop and resources for success.
- Unlimited skin checks for you, your family, and friends.
- Regular team events, including weekly drinks and monthly dinners.
- Be part of an enthusiastic, mission-driven team with global talent.
Research shows that while men apply to jobs when they meet an average of 60% of the criteria, women tend to only apply when they check every box. If you feel energized by our mission and would like to use your first-class talent to accelerate the growth of SkinVision, but don't necessarily meet every single point on the job description, please still apply. We'd love to receive your application and see if you could be a good fit.
- Please note that this position is open only to candidates residing in the Netherlands.