Pharmacovigilance Manager

Pharmacovigilance and Scientific Information Manager I am working exclusively with a long standing client who are a global leader in pharmaceutical generics manufacturing. Given the consistent success of the business over recent years, they are continuing to expand their portfolio and global presence. For this hire we are seeking an experienced and...

We are seeking a dedicated and skilled International Pharmacovigilance (IPV) Specialist to join our Global Safety & Pharmacovigilance (GSPV) team. The role is integral to supporting our IPV team and Safety Officer network in routine regional and operational activities. You will also play a critical role in developing and implementing strategies and projects...

What You'll Do:Monitor CROs and business partners for compliance with Safety Monitoring Plans, study plans, metrics, KPIs, and contractual agreementsLead pharmacovigilance (PV) compliance, inspection, and audit readiness for Argus, KPIs, and safety management topics.Oversee ICSR workflow, case management activities in Argus (or other safety databases),...

What You'll Do:Monitor CROs and business partners for compliance with Safety Monitoring Plans, study plans, metrics, KPIs, and contractual agreementsLead pharmacovigilance (PV) compliance, inspection, and audit readiness for Argus, KPIs, and safety management topics.Oversee ICSR workflow, case management activities in Argus (or other safety databases),...

Pharmacovigilance and Scientific Information Manager   I am working exclusively with a long standing client who are a global leader in pharmaceutical generics manufacturing. For this hire we are seeking an experienced and forward-thinking Pharmacovigilance (PV) and Scientific Information Manager who will lead on strategy development and work as the UK...

Senior Manager, CSV Auditor (Global Quality Management) Permanent, Full time (Paying up to £78,157 + benefits) Hybrid working - ad hoc travel required to their office near London (about once a month) and 30% travel to supplier sites across the globe. Our client, a global pharmaceutical company is seeking a CSV Auditor (Senior Manager, within the...

**Requisition Number**7925** **Employment Type**:Regular** **Who we are** Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s...

About the company:We are Qinecsa. Trusted partners to global life science companies. We bring together and offer best-in-class pharmacovigilance technology and scientific expertise to connect life science companies to the right safety solutions.Reportum platformOur automated case intake and follow up platform, Reportum, provides a centralized solution for...

About the Role: The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support...

About the Role: The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support...

Job Title: HR Project Delivery Specialist Company: Global Leading Pharmaceutical Company Contract Duration: Until 31st March 2025 (end of financial year) Full time (37.Location: Remote in the UK with 1day/month in Surrey office for meetings Our client is a global leading pharmaceutical company known with 10k plus employees worldwide. They are known...

Job Title: HR Project Delivery Specialist Company: Global Leading Pharmaceutical Company Contract Duration: Until 31st March 2025 (end of financial year) Full time (37.Location: Remote in the UK with 1day/month in Surrey office for meetings Our client is a global leading pharmaceutical company known with 10k plus employees worldwide. They are known...

One of our most exciting clients (top 10 pharmaceutical company) are seeking an Operations Manager for a field-based role across England. This position will be integral to the launch and delivery of cutting-edge CAR T cell therapy, ensuring NHS sites are fully prepared to provide these transformative treatments. It’s a unique opportunity to play a pivotal...

About the Role: The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support...

About the Role: The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support...

About the Role: The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support...

About the Role:The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support accurate...

About the Role:The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support accurate...

Senior Health Economist - United Kingdom - Global Pharmaceutical Company A global client of ours at Planet are now seeking a Health Economist to join the ever growing team! As our client continues to grow, we are excited to help recruit for their first Health Economist to the team. This role is ideal for someone with a true passion for illustrating the...

Senior Health Economist - United Kingdom - Global Pharmaceutical Company A global client of ours at Planet are now seeking a Health Economist to join the ever growing team! As our client continues to grow, we are excited to help recruit for their first Health Economist to the team. This role is ideal for someone with a true passion for illustrating the...