Primary Location:  London, England

Secondary Location: Barcelona, Spain

Working model:  Both locations have a hybrid working model (which requires 12 days per month in the office)

Note: Novartis is not able to offer relocation support for this role. Please only apply if this location is accessible for you.

Key Responsibilities: 

• Monitoring the clinical safety of projects /products including activities such as literature review, evaluation of individual cases or signal detection, and respond to safety related questions effectively.
• Perform medical assessment and related activities for cases whenever required, including collecting additional follow-up information as necessary, medical evaluation of product quality defects with adverse events, review of line listings of single cases, and preparation of investigator notifications and periodic medical assessments for ethics committees. 
• Identify safety signals based on the review of solicited or unsolicited single cases. Performing signal detection, monitoring and evaluation of all safety signals.
• Contributing towards responses to inquiries from regulatory authorities or health care professionals on safety issues.
• Preparing safety data for Health Authority review boards. Providing inputs to responses for legal queries and Country Organization requests involving safety issues.
• Providing expert evaluation on the clinical context of adverse event reports, assessment of the medical conditions, and the implications on Novartis products.
• Collaborate efficiently on clinical safety tasks with colleagues from Clinical Development, Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments.
• Contribute to the development of departmental goals and objectives.

Role Requirements:

Education & Experience:

• Medical Degree (Preferred) but PhD, PharmD also considered
• Sufficient experience in drug development in a major pharmaceutical company, including some years of experience in patient safety ideally in an operational or medical position.
• Experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications.
• Proven ability to analyse, interpret, discuss, and present safety information both in writing and orally.
• Experience in preparing or contributing to the preparation of clinical safety assessments and regulatory reports/submissions involving safety information.
• Experience with (safety or other) issue management.
• Global experience is required.

Languages :

• Fluent English (both spoken and written) is essential.
• Additional EU languages are an advantage.