Global Pharmacovigilance Risk Minimization Physician
Q-Med AB / Läkarjobb / Uppsala
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hela Sverige About Galderma
Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit
www.galderma.com. Job Description
Do you want to join a leader in skin solutions and be part of an international company in a growth phase? Do you want to be at the heart of product safety and influence on a global level? Then this can be the role for you!
The Risk Minimization Physician role is part of the new global R&D organization dedicated to Pharmaceuticals and Aesthetics. The Pharmacovigilance department's mission is to protect customers and patients from safety issues as well as lead the scientific and operational activities relating to the detection, assessment, understanding and prevention of adverse effects. The Pharmacovigilance Risk Management team is truly global, with colleagues based in the USA, Sweden, France and Switzerland. The Risk Minimization Physician role is located in Uppsala, Sweden, to interact closely with colleagues from the center of excellence for Aesthetics. The position is directly reporting to the Head of Pharmacovigilance Risk Management. Few business travels are included in the role, mostly within Europe and to Switzerland.
Job Responsibilities
As Global PV Risk Minimization Physician your mission will be to work with the benefit risk assessment for the Aesthetics product portfolio. Working with a cross-functional team, you will be accountable for the benefit-risk activities of Aesthetic products, including signal detection, risk management, risk mitigation plans, safety analyses in aggregate reports, medical review of ICSRs as needed etc.
You will lead the scientific review of safety-related information in CCDS, CSI, product labelling, investigator brochures, and DSUR/PSUR/PBRER, as well as respond to specific questions from Health Authorities.
As Risk Minimization Physician you will:
* Propose measures aiming at minimizing risks during clinical development;
* Organize and lead regular Product Safety Team meetings;
* Attend and present at Portfolio Safety Committee meetings as required;
* Review/provide input to Development Safety Update Reports (DSURs) and aggregate reports;
* Review/provide input to Risk Management Plans (RMP) and REMS;
* Review/provide input to Common Technical Document (CTD) or equivalent document for Dossier Registration and label;
* Contribute to Investigators/KOLs meetings for safety-related aspects/questions;
* Validate safety signals based on the review of single cases and aggregate data and escalate as appropriate;
* Ensure effective collaboration with stakeholders from the Clinical Development, Regulatory Affairs, Medical Affairs and Product Teams.
Minimum Requirements
You have a Medical doctor degree, combined with additional qualifications in clinical pharmacology and/or pharmacovigilance and drug safety.
You have worked for at least 10 years in pharmaceutical/medical device companies at a global level. You bring significant experience and knowledge of International clinical development and post marketing regulations applicable to medical devices primarily but also to drugs.
You have a sound knowledge of the safety requirements for non-clinical and clinical development, registration process and post-marketing of medical devices. You can identify signals and propose appropriate risk mitigation/minimization actions in complex and critical situations. You are also used to interact with Health Authorities in the US, EU and other geographies to address medical safety and risk management questions.
You speak English fluently and are used to working with cross-functional teams. You know how to communicate and influence others to ensure compliance and deliver within agreed timelines. As a representative for Pharmacovigilance, you possess high ethical standards and use sound medical judgement in your decision making.
What we offer in return
As Galderma's Global Center of Excellence for Aesthetics, we have in Uppsala a unique edge as we have on our site the whole chain from product development to production. Here, our 450 employees work on our world leading brands such as Restylane®, Azzalure® and Sculptra®.
We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala, only a 10-minute bike ride from Uppsala central station.
Your application
We welcome your application (CV and letter) preferably via this career site or via our company website
https://www.galderma.com/job-search. Apply as soon as possible though no later than February 15, 2021. The selection process is ongoing.
Should you have questions about this opportunity, you are welcome to contact Celine Bales, HR BP
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2021-02-05ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2021-02-15
Klicka på denna länk för att göra din ansökanFöretagQ-Med AB
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "109400047".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Q-Med AB (org.nr 556258-6882)
Arbetsplats Galderma
Jobbnummer 5560675
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