Senior Reproductive Toxicologist - Clinical Pharmacology and Safety Sciences (CPSS)
AstraZeneca · Mölndal, Sweden · Global
Regulatory Affairs
–
Not yet analysed
Demand65
Career growth60
Healthcare fit35
Remote potential40
5-year outlook
Likely competitive within senior pharma regulatory/toxicology roles, with pay varying by location and company band. Long-term demand should remain steady but niche, tied to drug pipelines and regulatory requirements.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-20
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering only if you already have DART/regulatory toxicology experience or a strong pharmacology/toxicology background plus industry exposure. Most clinicians without that specialised pharma experience should deprioritise it.
Who should apply
Physicians or pharmacists with toxicology, clinical pharmacology, drug safety or regulatory affairs experience, especially those who have supported submissions, labelling or health authority interactions. Not suitable for clinicians seeking an entry-level non-clinical transition.
CV angle
Frame real clinical pharmacology, drug safety, adverse-event assessment, paediatric/obstetric safety considerations, regulatory writing and cross-functional teamwork as evidence of safety-science judgement. Quantify any submission, labelling, guideline or health-authority contributions; do not claim DART programme leadership unless genuine.
Skills to highlight
- Reproductive and developmental toxicology
- Regulatory submissions
- Health authority interactions
- Product labelling
- Drug development lifecycle
- Safety pharmacology
- Scientific data interpretation
- Cross-functional leadership
Role summary
Senior pharma toxicology role providing reproductive and developmental toxicology expertise across drug development, regulatory submissions, labelling and health authority interactions.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.