Biotechnology Jobs in Maidstone

Director, Site Management & Monitoring[

Leads and develops a high-performing team responsible for site management and monitoring across clinical interventional studies, ensuring delivery within budget, timeline, and regulatory standards. Oversees site selection, initiation, monitoring, and closure while maintaining inspection readiness of trial documentation. Provides strategic guidance to study teams and contributes to regional and global initiatives within AstraZeneca’s clinical operations framework.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Buyer - Pharmaceuticals

This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.

Cranleigh Scientific Ditton, Kent, ME20 6AE, United Kingdom £22,800 – £28,800 pa

Hybrid Flexible

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Medical Director, Senior Patient Safety Physician

This role involves leading clinical safety strategy for drug projects across development and post-marketing phases, with a focus on oncology. The Medical Director will evaluate safety data from clinical and pre-clinical sources, contribute to global regulatory submissions, and guide risk management using advanced methodologies like signal detection and Safety Knowledge Groups. Based in Luton with a hybrid working model, the position drives patient safety within a global, science-led environment.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent Flexible

Medical Director, Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent