Medical Director, Senior Safety Physician

AstraZeneca; Barcelona; Presencial; EUR 100.000 - 150.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company seeks a Senior Medical Director, Senior Patient Safety Physician to lead and maintain high safety standards in drug development and post-marketing programs. The ideal candidate has a BS in medicine, over 7 years of experience in Pharmacovigilance, and a proven track record in clinical trials. This role is key in shaping departmental culture and ensuring compliance with clinical practices. Competencies in leadership and communication are essential. A PhD and therapeutic area expertise are preferred.

Formación

• 7+ years of proven experience in Patient Safety.
• Extensive experience in Pharmacovigilance with high standards.
• Detailed knowledge of safety reporting and surveillance processes.

Responsabilidades

• Provide strategic Patient Safety input to drug development.
• Collaborate on safety surveillance activities.
• Lead safety strategy for regulatory communication.

Conocimientos

Pharmacovigilance

Leadership

Communication

Clinical trials interpretation

Educación

BS degree in medicine

PhD in scientific field

Descripción del empleo

Medical Director, Senior Patient Safety Physician

As a Medical Director, Senior Patient Safety Physician, you are a senior leader within Patient Safety and play a key role bringing deep clinical understanding and judgement in benefit risk assessments for AstraZeneca products. You also have a role in shaping the culture of the department; and will act as a coach and mentor to more junior Patient Safety staff. You will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and regulatory requirements. We encourage you to closely follow medical developments within assigned areas to incorporate emerging data and trends into the safety strategy.

Main Responsibilities

• Providing strategic Patient Safety input to drug development and post-marketing programs
• Collaboration with team members to undertake safety surveillance activities and prepare high quality evaluation documents to describe safety findings.
• Ensuring expert input to all elements of design and interpretation, including efficient use of tools and methodology (e.g. modelling and simulation).
• Providing leadership to support project discussions with governance boards, including interactions with Patient Safety Peer Review Committee.
• Lead the safety strategy for regulatory communication and provide oversight of higher-level documents to support submission activities.
• Lead medico-scientific contributions to RMPs for assigned products and to Periodic Reports, including PBRERs, DSURs.
• More broadly you are expected to participate in advisory discussions to support other Patient Safety teams in the development of their safety strategy and may be asked to represent Patient Safety in cross-functional discussions with internal and external partners.

Minimum Requirements

• BS degree in medicine and experience as a physician or academic clinician
• 7+ years of proven experience
• Extensive experience in Pharmacovigilance, with clear evidence of delivering to a high standard
• Detailed understanding of pharmaceutical safety, reporting and surveillance processes and strong experience of Patient Safety, as it relates to clinical trials and marketed products in any relevant field such as pharma, Regulatory Agency or Public Health agency
• Experience in designing, supervising and implementing clinical trials and interpreting trial results
• Strategic leadership of complex drug projects
• Understanding of the medico‑legal aspects of pharmacovigilance
• Proven leader of cross‑functional delivery teams.
• Demonstrated ability to influence key business partners within and outside of company
• Proficiency with both written and verbal communications

Preferred

• PhD in scientific field
• 5+ years of proven experience
• Therapeutic area expertise and commercial understanding
• Extensive general medical knowledge
• Able to work across TAs and Functions
• Research background, including peer reviewed publications

Date Posted

13-Oct-2025

Closing Date

29-Nov-2025

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. 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.