Principal Clinical Scientist

Entity: CSL Seqirus

Job Category: Research Development \& Sciences

Job Family: Clinical Sciences

Job Type: Full Time

Location: Glattbrugg, Zürich, Switzerland

Employer Reference: R\-289968

Job Description
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Principal Clinical Scientist

*(Senior Clinical Scientist level also considered)*

The Role

We're looking for a clinical scientist — someone who has been the scientific lead for clinical studies before, from protocol development to start\-up (development of critical study documents) through to study execution, data analysis and interpretation and close\-out with a clinical study report. Having prepared regulatory submissions of study results is a pre. You'll work in close partnership with the clinical operations team and CROs under the team's full\-outsource operating model, managing that day\-to\-day relationship rather than delivering trial activity in\-house. It's one of two newly approved roles, created ahead of anticipated demand rather than to backfill a departure, which means there's genuine room to help shape how the team works rather than simply joining an existing structure.

*Hybrid based (3 days a week onsite) in Maidenhead (UK), Melbourne (Aus) or Zurich (CH)*

Why It Matters

A clinical study is only as good as the people running it. A weak protocol, poorly managed start\-up, or a fumbled relationship with the CRO delivering the trial can cost a program months — sometimes far more — and that delay sits between a therapy and the patients waiting on it. This role exists because CSL is adding capacity to get that execution right: someone who can lead all scientific needs of a study properly, and co\-own the end to end alongside clinical operations, is what actually moves a clinical development plan forward. It's not a supporting or administrative function — it's the core that determines whether the science translates into a trial that runs cleanly and data that holds up.

What You'll Be Responsible For

You'll take ownership of clinical studies end\-to\-end, acting as the scientific and operational anchor between the program team and outsourced delivery partners.

• Lead all scientific elements of clinical studies from protocol development through study execution to a final clinical study report


• Write and/or take responsibility for study protocols, clinical study reports and other critical study documents


• Manage, alongside the clinical operations lead, day\-to\-day working relationships with CROs under a full\-outsource operating model


• Collaborate closely with the cross\-functional study teams — this is a collaborative role, not an isolated one one


• Contribute to the scientific interpretation of clinical data and supporting documentation


• Build working relationships across the wider team, including colleagues based in the US and Australia

• Demonstrated, hands\-on experience with clinical studies (protocol development, execution, close\-out) — not solely oversight or academic exposure


• Experience writing clinical study protocols and clinical study reports directly


• Experience working within a full\-outsource / CRO\-dependent operating model


• A collaborative, cross\-functional working style — comfortable building relationships rather than working independently

CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state\-of\-the\-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits
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For more information on CSL benefits visit How CSL Supports Your Well\-being \| CSL.

You Belong at CSL
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At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion\-and\-belonging

Equal Opportunity Employer
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CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility\-statement.

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