Orthopedic Clinical Research Lead: Protocols & Compliance

Medartis; Basel; On-site; CHF 90,000 - 130,000; Full time

Job summary

Medartis, headquartered in Basel, Switzerland, seeks a qualified clinical research professional to lead and coordinate studies across sites worldwide. You will manage study protocol development, regulatory submissions, and data management while collaborating with internal and external stakeholders.

The role requires strong scientific background in a STEM field, experience with GCP, and willingness to travel up to 20%.

Qualifications

• Bachelor-level or higher in a STEM field; PhD desirable.
• GCP/ICH-GCP knowledge is preferred.
• Experience in clinical studies and regulatory requirements is advantageous.

Responsibilities

• Cultivate a portfolio of clinical research projects and sites.
• Maintain customer contacts through visits, trainings, and advisory support.
• Ensure quality system processes comply with regulatory and legal requirements.

Skills

English proficiency

Regulatory knowledge

Clinical research coordination

Fast learner

Willingness to travel

Education

PhD in STEM

GCP certificate desirable

Tools

EDC software

Office software

Job description

Medartis, headquartered in Basel, Switzerland, seeks a qualified clinical research professional to lead and coordinate studies across sites worldwide. You will manage study protocol development, regulatory submissions, and data management while collaborating with internal and external stakeholders.

The role requires strong scientific background in a STEM field, experience with GCP, and willingness to travel up to 20%.