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Position: Warehouse Associate Location: Chiswick, UK - Fully on-site Client: CRO Main Responsibilities • Handle the receipt, storage, and shipment of pharmaceutical and related products in line with company SOPs, • Support inventory control, including stock tracking and cycle counts using internal systems, • Maintain accurate and compliant documentation for shipments, receipts, and controlled substances, • Assist with logistics tasks, including arranging courier services when needed, • Contribute to warehouse upkeep, including equipment maintenance, validation activities, and safety checks (e.g. pest control, contingency testing), • Provide administrative support across warehouse operations, logistics, and quality teams, • Manage warehouse supplies and shipping materials to ensure smooth operations, • Ensure all activities comply with Good Distribution Practices (GDP) and internal quality standards Main Requirements • Bachelor’s degree preferred (ideally in science or supply chain), • Prior experience in logistics, supply chain, or temperature-controlled storage is an advantage, • Familiarity with inventory management systems/software preferred, • Ability to lift and move goods (up to 50 lbs) and operate warehouse equipment (e.g. pallet jack), • Strong organisation and time management skills, • Good written and verbal communication abilities, • Proficiency in Microsoft Office (especially Word and Excel), • ERP experience (preferred) ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Experienced Pharmacovigilance Lead (Hybrid role) This is NOT an entry level role. At least 3-5 years PV experience in a CRO is required. 6 month initial Fixed Term Contract Immediate start preferred The Pharmacovigilance Lead provides operational and scientific leadership for assigned projects and/or functional PV activities, ensuring delivery of high‑quality, compliant PV services in accordance with the TMC PV QMS, contractual obligations, and regulatory expectations. THIS IS A HYBRID ROLE: we expect the successful candidate be able to come to the office in Hartley Wintney, Hampshire, at least twice a week. Role-specific tasks include; Case processing, reporting and team management • Responsible for day-to-day oversight of end-to-end case processing, including management of PV rota, functional guidance, and leadership of case processing team, • Management of case-processing flow, ensuring regulatory reporting compliance., • Oversight of case-processing KPIs and maintaining and reporting on internal metrics and KPIs, • Provide expertise, support and active participation in case processing and routine departmental PV activities (e.g. MedDRA coding, eTMF, reconciliations), • Support PV Manager in preparation and maintenance of key client documentation (e.g. SMPs and PSMFS), • Ensure PV deliverables are executed, and delivered in compliance with the TMC PV QMS, SOPs, and applicable regulations., • Ensure inspection readiness for assigned projects, including support for audits and regulatory inspections., • Review and approve PV documents (inc. Project-specific and departmental controlled documents), reports, and outputs in line with delegated authority., • Support PV managers as point of contact for assigned clients or internal stakeholders., • Support PV governance activities, including oversight meetings, metrics review, and performance reporting. Other key information: Education and experience • Advanced life sciences degree (or equivalent experience)., • Significant experience in pharmacovigilance within a CRO and/or MAH environment., • Proven leadership and decision‑making capability., • Strong regulatory and scientific judgement., • Excellent stakeholder and client management skills., • Ability to balance operational delivery with quality and compliance oversight.

With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-prof

You will take ownership of end-to-end case processing oversight, ensuring compliance with global pharmacovigilance regulations while leading and developing a high-performing team. Strong experience in pharmacovigilance (CRO and/or MAH environment). We’re supporting a growing, international pharma

A leading global biopharma company is seeking a safety evaluation expert to lead pharmacovigilance and risk management activities.

A global biopharma company is looking for a professional to provide medical expertise in pharmacovigilance.

The role We’re looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. Key responsibilities* Lead and develop high-performing GCSP, Epidemiology, Medical

A global pharmaceutical company is seeking a Pharmacovigilance and Risk Management expert to lead safety evaluations and regulatory submissions.

A leading training organization in the United Kingdom is seeking a Pharmacovigilance Course Lead to design and deliver an industry-focused training program. This fully remote role requires 7–10+ years of experience in Pharmacovigilance and a strong ability to mentor future professionals.

As a senior member of the Pharmacovigilance (PhV) team within the Authorisations Division, you will help protect animal, environmental and public health through a globally recognised approach to pharmacovigilance. Senior Veterinary Pharmacovigilance Assessor. We have a vacancy for a Senior Veterinar

A global biopharmaceutical company in Greater London is seeking an experienced professional to lead Pharmacovigilance and Risk Management.

Ennov’s cloud-based solutions cover Regulatory Affairs, Pharmacovigilance, Quality, Clinical, and Document Management. Sales Executive – Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences). Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharm

A government agency in the UK is seeking a Senior Veterinary Pharmacovigilance Assessor responsible for post-authorisation surveillance of veterinary medicines.

Maintain inspection-ready safety documentation, including case records and Trial Master File (TMF) components, and lead or support regulatory inspections, audits, and internal quality reviews from a pharmacovigilance perspective. Support safety data reconciliation activities between pharmacovigilanc

Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. Demonstrate ability to learn quickly, adapt to a new process, and/or develop expertise in pharmacovigilance practices and safety regulations. Prior experienc

A global biopharma company in London is seeking a Pharmacovigilance Scientist with expertise in safety evaluation and risk management.

A leading life science consulting firm in the United Kingdom is seeking a Pharmacovigilance Manager to design and manage pharmacovigilance strategies.

A government veterinary agency in the UK seeks a Senior Veterinary Pharmacovigilance Assessor.

A government agency in the UK is seeking a Senior Veterinary Pharmacovigilance Assessor.

As a senior member of the Pharmacovigilance (PhV) team within the Authorisations Division, you will help protect animal, environmental and public health through a globally recognised approach to pharmacovigilance. Senior Veterinary Pharmacovigilance Assessor. We have a vacancy for a Senior Veterinar

Our client is currently seeking a Pharmacovigilance Manager in UK. Responsible for designing, implementing, and managing pharmacovigilance strategies and activities. Collaborate with cross-functional teams, regulatory authorities, and external partners to maintain a comprehensive pharmacovigilance s

Develop, maintain, and provide training on SOPs, PV processes, and procedures in accordance with Good Pharmacovigilance Practices (GVP)* Collaborate with cross-functional teams (clinical operations, regulatory affairs, medical affairs) to address safety issues and develop effective risk minimization

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A leading provider of pharmacovigilance solutions in the United Kingdom is seeking a Consulting Technology Project Manager. The ideal candidate will have over 8 years of project management experience, specifically in pharmacovigilance or regulatory technology projects.

A global pharmaceutical company is seeking a Pharmacovigilance Associate in Gloucestershire. Ideal candidates will have experience in pharmacovigilance, exceptional communication skills, and the ability to build strong relationships across teams.

A global biopharmaceutical company is seeking a Director, Pharmacovigilance to lead and oversee the PV operations across the UK & Ireland.

Review and summarize scientific literature relevant to pharmacovigilance. Strong knowledge and understanding of international safety reporting and pharmacovigilance requirements and signal detection. We are seeking a highly motivated and detail-oriented physician to join our growing Drug Safety & Ph

With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-prof

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Make extra money in a way that suits you — anytime, any day.Take charge of your earnings by becoming a self-employed delivery rider with Just Eat.Flexible hours – choose your own schedule and work when it suits you.Weekly pay – get paid, every week.No experience needed – just bring your moti