Clinical Research Manager — Global Studies & Compliance

Medartis

Basel

On-site

CHF 120,000 - 180,000

Full time

1 hour ago

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Job summary

Medartis in Basel is seeking a Clinical Research Scientist to lead clinical study programs and ensure regulatory excellence across sites worldwide.

You will design protocols, manage data collection, and coordinate with CROs, investigators, and regulatory bodies. Strong scientific writing and data analysis skills are essential, with up to 20% travel expected in a dynamic, international setting.

Qualifications

Degree in a STEM field or equivalent professional experience; PhD and GCP cert desirable.
Fluent English (spoken and written); other languages advantageous.
Willingness to travel up to 20%.
Experience in clinical studies and regulatory issues is preferred.

Responsibilities

Cultivate a portfolio of clinical research projects and sites to support Medartis regulatory requirements.
Create and maintain customer contacts, visits, trainings and advice as the liaison between internal and external partners.
Ensure processes comply with regulatory requirements (ICH-GCP, ISO 14155, lRB).
Coordinate with CROs and manage TMF/ISF; support study nurse(s) and site questions.
Proactively engage study institutions and investigators; oversee study protocols and data collection.
Contribute to statistical analysis and scientific writing for publications and presentations.