3 days ago

Clinical Trial Supply Manager

Actelion Pharmaceuticals Ltd

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Clinical Trial Supply Manager

Clinical Trial Supply Manager - (170000BF) Actelion Pharmaceuticals Ltd., a Janssen Pharmaceutical Company of Johnson &
Johnson, is recruiting for Clinical Trial Supply Manager. As part of the Janssen Pharmaceutical Companies of Johnson &
Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to
prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising
science. We collaborate with the world for the health of everyone in it. Actelion is a leader in the field of pulmonary
arterial hypertension (PAH). Our portfolio of PAH treatments covers the spectrum of disease, from WHO Functional Class
(FC) II through to FC IV, with oral, inhaled and intravenous medications. Job Responsibilities

- Ensure timely delivery of clinical trial supplies for assigned projects and studies
- Agree on project scope with the Clinical and the CMC teams, perform risk assessment and elaborate contingency
- Coordinate the production activities with regards to primary packaging (when appropriate), secondary packaging,
labeling and randomization at the supplier level
- Key contact to the suppliers for drug product packaging and distribution
- Set-up the worldwide study distribution to ensure proper distribution to the final consignees (investigational
sites) including the availability of import license or notifications
- Participation in the development and maintenance of internal quality rules and documents
- Approve the packaging and logistics service agreements with the CTS suppliers and corresponding invoices
- Regular update of the clinical supplies tracking and reporting using KPIs & annual reports

Candidate Requirements

- University degree or equivalent working experience in life sciences
- At least 2 years of experience in the field of Clinical Trial Supply (CTS)
- Up-to-date knowledge of the relevant international GMP, GDP, GCP regulations
- Excellent command of common study management tools
- Ability to work in international and cross functional teams
- English required, one additional language, preferably German or French is an asset

If you are interested in making an impact by working in a culture of innovation, trust and teamwork, we welcome your

Primary Location

: CH-BL-Allschwil


: Technical Operations


: Full-time

Job Type

: Standard

Job Posting

: Nov 8, 2017