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Unleash Your Potential

It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a global team with diverse culture where women and men are equals and share a passion for collaboration and solving complex problems.

Together, we help customers drive healthcare forward. We offer customized service, personalized to the need of our clients. Whether you are looking for full service CRO or staffing clinical or regulatory experts, our management team with more than 20 years experience will drive you to the effective solution.

HQ of ECLEVAR MEDTECH is Located in Paris, France

Working in France is a great opportunity and especially living in Paris is a multicultural metropolis that offers a wide range of opportunities.

Paris is a city where every corner has its little wonders: cafés, bakeries, bistros, and then theatres, gardens, picturesque districts… not to mention its Haussmann style architecture which gives it that splendid aspect of a city of great historical and artistic importance. You're gonna love it!

Eclevar Paris Office Eclevar Team

Salary and Working Hours at Eclevar MedTech

Salaries in Paris are high – up to 25% higher than in the rest of the country: not bad, right? If you are wondering what your professional life in Paris will be like, know that the workweek is set at 35/39 hours, with days starting around 9:30 am and ending around 7 pm.

Together, We Can Do Extraordinary Things

We work alongside customers and partners to be a catalyst for innovation in healthcare. ECLEVAR MEDTECH helps speed medical device development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access and delivery of healthcare, and ultimately drive better health outcomes.

ECLEVAR MEDTECH CORE+ makes the extraordinary possible by connecting patients to doctors and biological labs and connecting unparalleled data, advanced analytics, innovative technologies, and deep healthcare and scientific expertise so you can discover previously unseen insights, drive smarter decision-making, and unleash new opportunities.

Current Open Positions

Clinical Director – Japan

Clinical Operations Japan Full-Time

About the Role:

We are seeking an experienced Clinical Director to lead our clinical operations in Japan. This strategic role will oversee medical device clinical trials, ensure regulatory compliance with PMDA requirements, and build strong relationships with Japanese healthcare institutions and investigators.

Key Responsibilities:

  • Lead and manage clinical trial operations across Japan
  • Ensure compliance with PMDA regulations and Japanese clinical trial guidelines
  • Build and maintain relationships with key opinion leaders and clinical sites
  • Oversee study start-up, execution, and close-out activities
  • Manage cross-functional teams including CRAs, data managers, and medical writers
  • Provide strategic input on clinical development plans for the Japanese market
  • Collaborate with global teams to ensure alignment on study objectives

Required Qualifications:

  • 10+ years of clinical research experience in medical devices or pharmaceuticals
  • Deep understanding of PMDA regulations and Japanese clinical trial requirements
  • Proven track record of successfully managing complex clinical trials in Japan
  • Strong leadership and team management skills
  • Excellent communication skills in Japanese and English
  • Medical device industry experience strongly preferred

Nice to Have:

  • Experience with EU MDR and ISO 14155 standards
  • Network of Japanese investigators and clinical sites
  • Experience with PMCF studies and post-market surveillance

Senior Clinical Data Manager – France or UK

Data Management France or UK Full-Time

About the Role:

Join our data management team to oversee clinical data operations for medical device trials. You will be responsible for ensuring data quality, integrity, and compliance throughout the clinical trial lifecycle using our proprietary MILO Healthcare platform.

Key Responsibilities:

  • Lead data management activities for multiple medical device clinical trials
  • Design and implement eCRF databases using MILO Healthcare platform
  • Develop and execute data management plans and data validation specifications
  • Oversee data cleaning, query management, and database lock processes
  • Ensure compliance with ICH-GCP, EU MDR, GDPR, and 21 CFR Part 11
  • Collaborate with biostatistics, clinical operations, and medical writing teams
  • Mentor junior data management staff
  • Conduct quality control reviews and audits of clinical data

Required Qualifications:

  • 6+ years of clinical data management experience
  • Strong expertise with EDC systems (experience with MILO Healthcare a plus)
  • In-depth knowledge of ICH-GCP, EU MDR, and data privacy regulations (GDPR)
  • Experience with medical device trials preferred
  • Excellent attention to detail and problem-solving skills
  • Fluent in English; French proficiency is a plus

Nice to Have:

  • Experience with CDISC standards (CDASH, SDTM)
  • Knowledge of ePRO and eCOA systems
  • Programming skills (SAS, R, Python)
  • PMCF study experience

Clinical Project Manager – Germany (Preferably Munich)

Project Management Germany (Munich) Full-Time

About the Role:

We are looking for an experienced Clinical Project Manager to lead medical device clinical trials in Germany. You will manage all aspects of study execution, from site initiation to database lock, ensuring timely delivery and compliance with EU MDR and ISO 14155 standards.

Key Responsibilities:

  • Manage end-to-end execution of medical device clinical trials in Germany
  • Develop and maintain project plans, timelines, and budgets
  • Coordinate cross-functional teams including CRAs, data managers, and regulatory specialists
  • Oversee site selection, initiation, monitoring, and close-out activities
  • Ensure compliance with EU MDR, ISO 14155, and ICH-GCP guidelines
  • Manage relationships with clinical sites, investigators, and ethics committees
  • Identify and mitigate project risks proactively
  • Provide regular status updates to sponsors and senior management

Required Qualifications:

  • 5+ years of clinical project management experience
  • Strong knowledge of EU MDR, ISO 14155, and German clinical trial regulations
  • Experience managing medical device trials (Class IIa, IIb, or III)
  • Excellent organizational and leadership skills
  • Strong communication skills in German and English
  • Proven ability to manage multiple projects simultaneously

Nice to Have:

  • PMP or equivalent project management certification
  • Experience with PMCF studies and registries
  • Network of German clinical sites and investigators
  • Experience with EDC platforms (MILO Healthcare a plus)

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Reforming Clinical Evaluation of Medical Devices in Europe