Empleos actuales relacionados con Associate Director, Patient Safety Scientist - Barcelona - AstraZeneca

  • Associate Director, Patient Safety Scientist

    hace 25 minutos

    Barcelona, España AstraZeneca GmbH A tiempo completo

    **Job Title: Associate Director, Patient Safety Scientist** **Global Career Level: E** **Introduction to role**: The Associate Director, Patient Safety Scientist role works collaboratively with the Global Safety Physician (GSP) and Senior Patient Safety Scientist to review safety data and related documents for potential safety issues. This role involves...

  • Associate Director, Patient Safety Scientist V&i

    hace 2 semanas

    Barcelona, España AstraZeneca A tiempo completo

    **Role**:Associate** Director, Patient Safety** Scientist** **Location: Onsite with Flexibility in Gaithersburg MD, or Waltham MA, or Barcelona SP, or Cambridge UK, Warsaw PO, or Gothenburg SW** At AstraZeneca, we work together to deliver innovative medicines to patients across global boundaries. We make an impact and find solutions to challenges. We do...

  • Associate Director, Patient Safety Scientist

    hace 2 días

    Barcelona, España AstraZeneca A tiempo completo

    **_Would you like to use your drug safety or pharmacovigilance experience to make a difference to the lives of millions of patients across the world? If you would, please read on!_** At AstraZeneca, we work together to deliver innovative medicines to patients across global boundaries. We make an impact and find solutions to challenges. We do this with...

  • Director, Principal Patient Safety Scientist Oncology

    hace 1 semana

    Barcelona, España AstraZeneca A tiempo completo

    Director, Principal Patient Safety Scientist OncologyBarcelona, Spain (on-site) 3 days working from the office and 2 days working from home. AstraZeneca is a global, science‑led, patient‑focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious...

  • Director, Principal Patient Safety Scientist Oncology

    hace 1 semana

    Barcelona, España AstraZeneca A tiempo completo

    Director, Principal Patient Safety Scientist Oncology Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home. AstraZeneca is a global, science‐led, patient‐focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most...

  • Director, Principal Patient Safety Scientist Oncology

    hace 1 semana

    Barcelona, España AstraZeneca A tiempo completo

    Location Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home. Would you like to apply your expertise to lead on complex PV projects in a company that follows the science and turns ideas into life changing medicines? AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the...

  • Director, Principal Patient Safety Scientist Oncology

    hace 2 semanas

    Barcelona, España AstraZeneca A tiempo completo

    **Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home.** AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the...

  • Manager Patient Safety Scientist

    hace 1 semana

    Barcelona, España AstraZeneca A tiempo completo

    At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality._ **Patient Safety at AstraZeneca is now looking for** **Pharmacovigilance (PV) Scientists to join our Patient Safety BioPharma team.** The positions will be based in Barcelona, Spain. We...

  • Associate Director, Senior Patient Safety Scientist Oncology

    hace 2 semanas

    Barcelona, España AstraZeneca A tiempo completo

    **Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home.** **_Would you like to use your drug safety or pharmacovigilance experience to make a difference to the lives of millions of patients across the world? If you would, please read on!_** At AstraZeneca, we work together to deliver innovative medicines to...

  • Associate Director, Safety Scientist, Gds

    hace 10 minutos

    Barcelona, España AstraZeneca A tiempo completo

    **Associate Director, Safety Scientist Location**: Barcelona, SpainReporting to: Executive Medical Director Onsite with flexibility (2 days remote) This is what you will do: The Associate Director, Safety Scientist plays a leadership role within Global Drug Safety to actively evaluate and manage risk in collaboration with the GDS Medical Director and...

Associate Director, Patient Safety Scientist

hace 2 semanas

Barcelona, España AstraZeneca A tiempo completo

**Location: Onsite 3 days/week in Barcelona**

At AstraZeneca we turn ideas into life-changing medicines. Working here means being ambitious, thinking big and working together to make the impossible a reality. We do this with integrity even in the most difficult situations because we are committed to doing the right thing.

**Patient Safety BioPharma at AstraZeneca is now looking for** **a Patient Safety Scientist to join our team**.

The core purpose of AstraZeneca Patient Safety is to add value to AstraZeneca products, provide clear science-based guidance for investigators and prescribers to safeguard patients as well as the success of our business. Patient Safety covers the entire clinical life cycle of a drug from first time into man to withdrawal of a product from the market.

As a **Patient Safety (PS) Scientist**, you work with Patient Safety Physicians and other PV Scientist(s) with review, analysis and interpretation of safety data obtained from patients who have been administered the assigned medicinal products in clinical development programs and/or from marketed use. You provide authoring and input to safety documents and regulatory reports and lead internal and external meetings to present safety data and analyses. You evaluate the clinical implications of safety data from pre-clinical studies, clinical studies, literature, and other information sources to establish the safety profile of drugs and manage the risk to patients.

**Main Responsibilities**
- Leads and/or conducts proactive pharmacovigilance and risk management planning for designated products, including preparation of safety aspects of Global Risk Management Plans, in partnership with the Global Safety Physician (GSP) and others as appropriate.
- Represents Patient Safety on cross-functional project teams for developmental compounds and/or marketed products.
- Presents issues to Safety Information Review Committee (SIRC) and has the capacity to take the lead role in data evaluation and discussion of the results with the SIRC Chair, GSP and other key stakeholders.
- Produces accurate and fit for purpose evaluation documents with clear conclusions in response to internal or regulatory authority requests for safety data.
- Collaborates with GSP and Clinical representatives and authors the Reference Safety Information (RSI) for assigned development products; coordinates meetings and tracks timelines to ensure completion.
- Authors/provides strategic input or oversight for periodic regulatory documents (PBRERs, PSURs, DSURs) according to the agreed process and timelines.
- Authors/provides strategic input to regulatory submissions for new products, formulations, or indications (NDA/BLA, MAA), in partnership with the GSP and other functional experts.
- Contributes to the PS component of contracts/agreements with third parties to ensure quality and integrity of agreement.
- Trains junior members of the team in Patient Safety tools and systems

**Minimum Education, Experience and Skill Requirements**
- A life sciences/pharmacy/nursing degree and demonstrated Patient Safety and/or Clinical/ Drug Development experience.
- Intermediate knowledge of pharmacovigilance regulations
- Fluent in written and verbal English
- Basic understanding of epidemiology

If you would like to be notified about future job opportunities, you can set up a job alert Click on the **Career** icon on the Workday homepage and select **Manage job alerts.