Senior Safety Analysis Scientist, Pharmacovigilance Lead

Johnson & Johnson Innovative Medicine; High Wycombe; Hybrid; GBP 90,000 - 140,000; Full time

Benefits offered by this job

Hybrid work model

On-site 3 days a week

Job summary

Johnson & Johnson Innovative Medicine is seeking an Associate Director, Safety Analysis Scientist (SAS) based in High Wycombe, UK. This hybrid role requires on-site presence three days per week to lead safety evaluations and collaborate with SMTs to shape safety strategy.

You will oversee data analyses, write safety reports, and mentor team members, driving regulatory-compliant safety assessments for marketed and developmental products.

Qualifications

• Medical writing or PV experience required.
• Ability to analyze complex medical data.
• Excellent English verbal and written communication skills.
• Ability to lead cross-functional teams and manage multiple priorities.

Responsibilities

• Lead safety evaluations including strategy discussions, data retrieval and report writing.
• Ensure high quality safety evaluations and reports with minimal revisions.
• Provide input and review of regulatory/clinical documents as appropriate.
• Demonstrate leadership in the SMT and support the MSO.
• Support SMT activities and compile meeting minutes.

Skills

Medical writing

Pharmacovigilance

Safety data analysis

Regulatory knowledge

English communication

Education

Bachelor’s Degree in Healthcare/Biomedical Science

Advanced Degree preferred

Tools

Microsoft Word

Excel

PowerPoint

Veeva

Job description

Johnson & Johnson Innovative Medicine is seeking an Associate Director, Safety Analysis Scientist (SAS) based in High Wycombe, UK. This hybrid role requires on-site presence three days per week to lead safety evaluations and collaborate with SMTs to shape safety strategy.

You will oversee data analyses, write safety reports, and mentor team members, driving regulatory-compliant safety assessments for marketed and developmental products.