Description
**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.**
**If you're ready to make a real impact - this is your moment.**
We are currently looking for a motivated and collaborative professional to join our Clinical Safety & Pharmacovigilance team based at our Headquarters in Lausanne, Switzerland as
### **Associate Safety Physician - P2603 ** ###
In this role, you will actively manage and evaluate Safety Data for products in development, working under the guidance of the Executive Safety Physician or the Head of Clinical Safety.
**Your Mission **
* Medical Safety Oversight: Manage project safety profiles and conduct individual/aggregate medical reviews within the safety database.
* Clinical Support: Provide expert medical input for study protocols, Investigator Brochures (IBs), and Development Safety Update Reports (DSURs).
* Signal Detection & Surveillance: Lead ongoing safety monitoring and signal detection, particularly during early-phase clinical trials.
* Cross-Functional Collaboration: Partner with Clinical, Regulatory, and Biostatistics teams to ensure clinical programs support robust safety assessments.
* Stakeholder Representation: Represent Safety in study teams, internal task forces, and external meetings like IDMCs.
* Regulatory & Compliance: Contribute to safety sections of IND/NDA submissions and maintain inspection readiness for audits/inspections.
*More than a checklist of skills, we-re looking for someone who shares our commitment to science with purpose. *
**Your profile **
* Medical Credentials: Medical Doctor (MD) with 2/3years of clinical/pharma experience or a Physician with research fellowship experience.
* Technical Expertise: Proven ability in medical review, data analysis, and safety surveillance within clinical studies.
* Regulatory Knowledge: Solid foundational understanding of GCP and Pharmacovigilance (PV) principles.
* Communication Mastery: Excellent English verbal and medical writing skills, with the ability to simplify complex terminology.
* Matrix Efficiency: Ability to thrive in a high-stress matrix environment, collaborating effectively across all organizational levels.
* Operational Excellence: Strong problem-solving skills with a track record of meeting deadlines and maintaining high quality standards.
**What we Offer: **
* 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.