Senior Director Physician – Renal SKG Lead

AstraZeneca; Barcelona; Presencial; EUR 90.000 - 110.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Barcelona seeks a Renal Safety Knowledge Group Lead to manage activities related to drug-induced renal toxicity. This role requires a Medical Practitioner with at least 5 years of drug development experience, specialized in Nephrology. The ideal candidate will lead strategic projects while providing scientific and medical input to ensure safety evaluations meet regulatory requirements. Strong influencing and communication skills are essential for success in this global role.

Formación

• Must be a Medical Practitioner with a minimum of 5 years drug development experience.
• Board certified in Nephrology or a related specialty.
• Experience with regulatory agency interactions is required.

Responsabilidades

• Lead projects related to monitoring and mitigating renal toxicity in clinical trials.
• Provide strategic direction on issues related to drug/biological renal toxicity.
• Collaborate on biomarker development related to renal toxicity.

Conocimientos

Drug development experience

Nephrology specialty

Influencing skills

Verbal communication

Written communication

Conceptual thinking

Strategic vision

Educación

Medical practitioner degree

Descripción del empleo

The clinical Renal Safety Knowledge Group (SKG) Lead manages a diverse range of activities related to monitoring, diagnosis, and mitigation of drug/biological‑induced renal toxicity in a matrix environment. The role holder inspires, manages, and leads cutting‑edge projects to better understand and characterise drug/biological‑induced renal toxicity on a global basis. The Renal SKG Lead will be influencing the shaping of the organisation by providing strategic direction and applying a full understanding of global issues related to drug/biological‑induced renal toxicity. The role leads efforts related to renal safety within the broader AZ organisation.

Responsibilities

• Acts as an expert involved in the design, conduct, monitoring, data interpretation and reporting of potential clinical safety signals related to renal toxicity which arise during the conduct of clinical trials.
• Manages global research projects for state‑of‑the‑art detection, management, and mitigation of clinical safety signals related to renal toxicities.
• Ensures the research projects related to drug‑induced renal toxicity adhere to Good Clinical Practice and regulatory requirements.
• Acts as a renowned expert in own field to provide expert scientific and medical input to Global Patient Safety activities, with special focus on cross‑project and cross‑TA activities of a scientific nature.
• Leads and endorses the development of scientific methods applied to a wide range of safety data related to drug‑induced renal toxicity.
• Promotes safety sciences and clinical safety across projects and therapeutic areas.
• Provides support, as needed, for discussions with internal governance and international regulatory bodies.
• Contributes to improved understanding and prevention of drug/biological‑induced renal toxicity issues across functions within the company and across Pharmaceutical Companies and Regulatory Authorities.
• Contributes to the implementation of the Global Patient Safety strategy, and to the successful implementation of the global working model for Clinical Safety.
• Leads the drug/biological‑induced renal toxicity biomarker development and collaborates with the Preclinical SKG lead on preclinical strategies.

Essentials

• Medical practitioner with at least 5 years drug development experience.
• Specialised in Nephrology or related specialty (board certified).
• Regulatory Agency interactions (authoring briefing documents / regulatory responses / label discussions).
• Leading cross‑functional teams.
• Broad knowledge of drug development and global regulatory requirements with regards to renal‑specific safety evaluation, safety reporting and risk management strategies.
• Influencing skills, excellent verbal and written communication skills.
• Capable of conceptual thinking and strategic vision with respect to renal toxicity.
• Ability to identify and mitigate against renal toxicity risks.
• Ability to establish causality in cases of renal injury.
• Ability to define best practices in renal safety.

Desirable

• At least 2 years of patient safety experience.
• Setting up internal and external collaborations (e.g. safety consortia) to promote organ safety.
• Demonstrated experience in adopting new technology (biomarkers, etc.).
• Strategic thinking and influencing with respect to renal safety.

Date Posted 12-Dec-2025

Closing Date 30-Jan-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry‑leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non‑discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.