Start up Specialist Switzerland

Resourcing Life Science Ltd.

Schweiz

On-site

CHF 90,000 - 120,000

Full time

14 days+

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Job summary

Resourcing Life Science Ltd. is seeking a Start up Specialist for a Global CRO, based in Switzerland. The role focuses on EC and CA submissions, ensuring accuracy and regulatory compliance for II-III studies, and supporting translations for submission documents.

The candidate will keep current with GCP and ICH guidelines, coordinate translations, and supervise study conduct in line with applicable laws. Fluent in English and German, Bachelor in life sciences, and at least one year of relevant

Qualifications

Bachelor degree in life-science.
At least 1 year in EC & CA submissions within a CRO, pharma or biotech in Switzerland.
Experience in clinical studies phase II–III.
Fluency in English and German.

Responsibilities

Responsible for CA & EC submission.
Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
Translation and co-ordination of translations for documents required for submissions.
Supervising study conduct according to GCP requirements and all applicable laws.

Skills

English

German

Education

Bachelor's degree in life-science

Job description

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist in Germany with fluent Switzerland.

Job Overview

Responsible for CA & Ethics Committee (EC) submission
Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
Translation and co-ordination of translations for documents required for submissions.
Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements