4 Drug Safety jobs in the United Kingdom

Our client is a market leader within the Pharma Covigilance market. They are looking to recruit a Drug Safety Administrator who will be an active participant in meetings and assist the PV Manager in maintaining standard operating procedures or working practices. During their daily activities, the Drug Safety Administrator will be required to liaise with pharmaceutical companies and other business partners.

Daily tasks:

• Keeping the Pharmacovigilance Manager fully informed of problems and issues that may arise related to the product, adverse events, the patients, prescribers or the marketing authorisation holder.
• Processing selected case reports in the database.
• Checking all literature case reports have the appropriate AE terms assigned for MedDRA coding. Notifying the QPPV of cases where the appropriate MedDRA term cannot be identified independently.
• Reconciliation both with clients and/or with PV partners on behalf of clients (as required).
• Processing reports from any source in the drug safety database.
• Assessing adverse events and carry out listedness and causality assessments.
• Exchanging a PV case reference from the database with PV partners.
• Conducting follow-up investigation for direct reports from either patients or healthcare professionals.
• Maintaining Continued Professional Development in support of your role and responsibilities.
• Participate in various team meetings and liaise with other colleagues about on-going projects.
• Assist with documentation such as Working Practices and Standard Operating Procedures, where required.
• Develop a thorough knowledge of medicinal products and with regulations and guidelines within the industry.
• An organised, proactive person with excellent attention to detail.
• Excellent oral and written communication with proficiency in standard software programs.

Minimum Requirements:

• Life science or Bio medical graduate (1-2 years working experience desirable) or other allied healthcare professional.

Please note candidates will only be considered with the above skills and unfortunately this company cannot consider sponsorship, or a visa status that will need renewing.

CPL Life Sciences are in collaboration with a world-renowned global pharmaceutical company who are seeking two new professionals at varying experience levels to join their Safety Science and Pharmacovigilance team. This role provides scientific safety oversight across the full lifecycle of investigational and marketed products.

As a Safety Scientist, you key responsibilities will include:

• Support safety activities in early and late-phase clinical development
• Conduct signal detection, evaluation, and contribute to risk-benefit assessments
• Manage individual case safety reports (ICSRs) and prepare aggregate reports (e.g., DSURs, PBRERs)
• Participate in the preparation and review of regulatory submissions (INDs, NDAs, MAAs, etc.)
• Contribute to the development and maintenance of safety labeling and core safety documents
• Collaborate with internal teams and external partners to ensure high-quality safety deliverables
• Provide safety input to study teams and participate in cross-functional meetings
• Help prepare materials for safety committees (e.g., iDMCs, IMCs) and regulatory authorities

Hybrid: North London 2 days per week on site, 3 days remote

Applicants should have direct experience working with signal detection, aggregate reports and risk management plans in particular for both clinical and post-marketing activities.

Strong analytical, communication, and collaboration skills are essential for success in this role.

CPL Life Sciences are in collaboration with a world-renowned global pharmaceutical company who are seeking two new professionals at varying experience levels to join their Safety Science and Pharmacovigilance team. This role provides scientific safety oversight across the full lifecycle of investigational and marketed products.

As a Safety Scientist, you key responsibilities will include:

• Support safety activities in early and late-phase clinical development
• Conduct signal detection, evaluation, and contribute to risk-benefit assessments
• Manage individual case safety reports (ICSRs) and prepare aggregate reports (e.g., DSURs, PBRERs)
• Participate in the preparation and review of regulatory submissions (INDs, NDAs, MAAs, etc.)
• Contribute to the development and maintenance of safety labeling and core safety documents
• Collaborate with internal teams and external partners to ensure high-quality safety deliverables
• Provide safety input to study teams and participate in cross-functional meetings
• Help prepare materials for safety committees (e.g., iDMCs, IMCs) and regulatory authorities

Hybrid: North London 2 days per week on site, 3 days remote

Applicants should have direct experience working with signal detection, aggregate reports and risk management plans in particular for both clinical and post-marketing activities.

Strong analytical, communication, and collaboration skills are essential for success in this role.