Beschreibung

***At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases. As a privately-owned Swiss biopharmaceutical company, we-re driven by science, but above all, by the people behind every treatment - the patients and their families.***

***Through our unique -development only- model, we bring forward promising therapies and transform them into treatments that can reach those who need them most, faster.***

Are you passionate about patient safety and drug development? Join our Clinical Safety & Pharmacovigilance (CS&PV) team for a maternity cover position, and contribute to the development of innovative therapies in Oncology and Infectious Diseases.

We are currently looking for a motivated and collaborative professional to join our Clinical Development department at our Headquarters in Lausanne, Switzerland as

**Associate Clinical Safety Officer (100% - Maternity Cover)**

Reporting to the Clinical Safety Manager, you will actively support the safety surveillance and pharmacovigilance activities for a portfolio of clinical-stage compounds, ensuring compliance and operational excellence across all phases of development.

**Your Mission.**

Pharmacovigilance Surveillance

* Manage case processing and electronic reporting for clinical trials under the supervision of the Clinical Safety Manager.
* Participate in multidisciplinary study team meetings alongside Clinical Safety Officers.
* Collaborate with internal teams, vendors, CROs, and partners to execute CS&PV activities.
* Support reconciliation between clinical and safety databases.
* Coordinate the preparation of DSURs and Safety Management Plans.
* Contribute to safety surveillance and signal detection activities in collaboration with Safety Physicians.

Operations & Quality Assurance

* Ensure appropriate filing of clinical safety documents in Trial Master Files (TMFs).
* Support the development and compliance of SOPs and working instructions.
* Assist in vendor oversight and performance management.

*More than a checklist of skills, we-re looking for someone who shares our commitment to science with purpose.*

* PhD or MSc in Sciences Pharmacy, Medical Biotechnology, or a related field.
* Minimum 2 years- experience in clinical trial safety within a vendor, academic institution, or pharmaceutical company.
* Experience working on clinical trials in development (Phase 1 and 2 required; Phase 3 is a plus).
* Familiarity with safety databases and exposure to PV tools (XEVMPD, EudraVigilance training is a plus).
* Scientific acumen to support review of study reports and contribute to safety deliverables.
* Excellent medical writing and editorial skills in English
* Previous experience in Oncology or Infectious Diseases is an advantage.
* Strong interpersonal and communication skills; experience working in matrix organizations.
* Problem-solving mindset, flexibility, and a team-oriented attitude.

* Being part of a company where innovation, collaboration, and impact aren-t just values - they-re how we work every day
* Partner with teams across disciplines, at the forefront of oncology and anti-infective development
* An inclusive and respectful workplace - proud to be Equal-Pay certified
* Grow in a culture that values people, purpose, and performance
* A chance to grow, share, and shape the future of healthcare

 

**What to Expect in the Recruitment Process:**

If your application is selected, you-ll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams, followed by a panel interview and reference checks. Communication is handled via Workable-check your spam folder for emails from *\*@outbound.workable.com*.

*Please contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.*