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Planet Pharma
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  • Commercial and Industry Expert (Expert Witness) - EU Medical Devices  

    Planet Pharma
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    Planet Pharma are currently partnered with a leading pharmacy group an... Read More
    Planet Pharma are currently partnered with a leading pharmacy group and we are actively seeking a Commercial and Industry Expert (Expert Witness) - EU Medical Devices to join the business on a freelance basis. Key Responsibilities: Provide independent commercial and industry expertise in support of an international arbitration matter within the European medical devices sector. Analyse and interpret market conditions, commercial trends, and industry dynamics across relevant European healthcare markets. Evaluate business, regulatory, and competitive factors affecting medical device commercialisation, licensing, and distribution strategies. Review and assess relevant commercial agreements, including supply, licensing, and distribution arrangements, and provide expert insight on industry standards and practices. Conduct market assessments using sector knowledge, commercial data, and relevant benchmarks to support expert opinions and conclusions. Prepare detailed expert reports, written opinions, and supporting analyses in accordance with arbitration requirements. Work collaboratively with legal teams and other stakeholders to develop clear, evidence-based expert testimony. Provide oral testimony and participate in hearings, depositions, or expert discussions as required. Explain complex medical device market, regulatory, and commercial considerations in a clear and accessible manner for legal and non-industry audiences. Maintain independence, objectivity, and confidentiality throughout the engagement. Stay informed on European medical device regulations, reimbursement environments, market access considerations, and evolving industry trends relevant to the matter. Key Requirements: Extensive experience within the European medical devices industry, gained through roles such as commercial strategy, market analysis, business development, consulting, or industry leadership. Strong understanding of medical device regulatory frameworks and market dynamics across Europe. Previous experience acting as an expert witness or providing expert advisory services in litigation or international arbitration. 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. www.planet-pharma.com Please click ‘apply’ or contact Harry Banks at Planet Pharma for more information: E: hbanks@planet-pharma.co.uk Read Less
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  • Warehouse Operative / Forklift Driver  

    Planet Pharma
    - Kent
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    Warehouse Operative / Forklift Driver 📍 Kent Science Park, Kent 🕒 Full... Read More
    Warehouse Operative / Forklift Driver 📍 Kent Science Park, Kent 🕒 Full-Time | Site-Based We're looking for an experienced Warehouse Operative / Forklift Driver to join a busy warehouse and supply chain operation in Kent. This role is ideal for someone with strong warehouse experience, excellent attention to detail, and a valid forklift licence who enjoys working in a fast-paced environment. You'll be responsible for the safe movement, storage and distribution of materials and products, while maintaining accurate inventory records and supporting day-to-day warehouse operations. Key Responsibilities Operating reach trucks, counterbalance forklifts, stackers and electric pallet trucks Receiving and booking in deliveries from suppliers Loading, unloading and moving stock safely within the warehouse Picking, packing and distributing materials to internal customers Maintaining accurate stock records and inventory transactions within the ERP system Conducting routine cycle counts and supporting stock audits Supporting goods-in, goods-out and dispatch activities Ensuring all warehouse activities are completed in line with safety and quality standards Working closely with Supply Chain, Manufacturing and Warehouse teams to ensure materials are available when required. What We're Looking For Essential Valid licences and practical experience operating:Reach Truck Counterbalance Forklift Stacker Truck Electric Pallet Truck Previous warehouse, logistics or stores experience Good computer literacy Experience using ERP, warehouse management or inventory systems Strong attention to detail and accuracy Ability to manage stock transactions and inventory records Good communication skills and a team-focused approach Ability to work efficiently in a fast-paced operational environment Desirable Experience within pharmaceutical, manufacturing or regulated environments Understanding of inventory control and stock management processes Experience supporting shipping and distribution activities. What's on Offer? Opportunity to join a growing and collaborative operation Stable, full-time position Varied warehouse and logistics responsibilities Supportive team environment Ongoing training and development opportunities If you're an experienced forklift driver with strong warehouse and systems experience, we'd love to hear from you. Apply now to be considered. Read Less
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  • Global Clinical Program Director  

    Planet Pharma
    - Greater London
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    p strong Summary /strong /p p Exciting opportunity with a global biote... Read More
    p strong Summary /strong /p p Exciting opportunity with a global biotech organisation seeking an experienced Clinical Operations leader to drive clinical development strategy and execution across the full product lifecycle—from First-in-Human studies through registration and post-marketing activities. This is a highly visible leadership role, combining strategic oversight, operational excellence, and cross-functional collaboration on global development programs. /p p br /p p strong Responsibilities: /strong /p ul li Lead clinical operations strategy and provide input into global Clinical Development Plans (CDPs) and program objectives. /li li Oversee clinical development activities across assigned indications and ensure delivery against timelines, budgets, and quality expectations. /li li Drive operational risk management, issue resolution, and cross-functional decision-making. /li li Partner with Clinical Trial Leads, Project Managers, and senior stakeholders to ensure successful execution of global clinical programs. /li li Support country and site selection, CRO management, and regulatory readiness activities. /li li Lead and mentor clinical operations teams, fostering a culture of collaboration, innovation, and continuous improvement. /li li Ensure inspection readiness and support audits across the development portfolio. /li /ul p br /p p strong Requirements: /strong /p ul li 15+ years of experience in Clinical Development and Clinical Operations leadership within biotech or pharmaceutical organisations. /li li Strong background in global clinical trial management, strategic drug development, and operational execution. /li li Proven experience leading complex global programs and working effectively within matrix environments. /li li Experience managing CROs, external partners, and outsourced clinical development models. /li li Strong leadership, stakeholder management, and team development capabilities. /li li Thorough knowledge of ICH-GCP and global clinical development regulations. /li li Degree in Life Sciences, Biomedical Sciences, Pharmacy, Medicine, or a related discipline. /li /ul p br /p p strong u ABOUT PLANET PHARMA /u /strong /p p br /p p Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters 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. /p p Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized 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. /p p 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. /p p a www.planet-pharma.com /a /p p br /p p strong u TO APPLY /u /strong /p p Please click ‘apply’ or contact Joesela Alolod A. (Recruitment Sourcer) at Planet Pharma for more information: /p p br /p p strong E: /strong JAnzures@planet-pharma.com /p p strong T: /strong +61 370580550 /p p strong Linkedin: /strong a www.linkedin.com/in/joeselaaloloda/ /a /p p /p Read Less
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  • Global Clinical Program Director  

    Planet Pharma
    - Greater London
    Apply Now
    Summary Exciting opportunity with a global biotech organisation seekin... Read More
    Summary Exciting opportunity with a global biotech organisation seeking an experienced Clinical Operations leader to drive clinical development strategy and execution across the full product lifecycle—from First-in-Human studies through registration and post-marketing activities. This is a highly visible leadership role, combining strategic oversight, operational excellence, and cross-functional collaboration on global development programs. Responsibilities: Lead clinical operations strategy and provide input into global Clinical Development Plans (CDPs) and program objectives. Oversee clinical development activities across assigned indications and ensure delivery against timelines, budgets, and quality expectations. Drive operational risk management, issue resolution, and cross-functional decision-making. Partner with Clinical Trial Leads, Project Managers, and senior stakeholders to ensure successful execution of global clinical programs. Support country and site selection, CRO management, and regulatory readiness activities. Lead and mentor clinical operations teams, fostering a culture of collaboration, innovation, and continuous improvement. Ensure inspection readiness and support audits across the development portfolio. Requirements: 15+ years of experience in Clinical Development and Clinical Operations leadership within biotech or pharmaceutical organisations. Strong background in global clinical trial management, strategic drug development, and operational execution. Proven experience leading complex global programs and working effectively within matrix environments. Experience managing CROs, external partners, and outsourced clinical development models. Strong leadership, stakeholder management, and team development capabilities. Thorough knowledge of ICH-GCP and global clinical development regulations. Degree in Life Sciences, Biomedical Sciences, Pharmacy, Medicine, or a related discipline. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters 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 recognized 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. www.planet-pharma.com TO APPLY Please click ‘apply’ or contact Joesela Alolod A. (Recruitment Sourcer) at Planet Pharma for more information: E: JAnzures@planet-pharma.com T: +61 370580550 Linkedin: www.linkedin.com/in/joeselaaloloda/ Read Less
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  • Senior Director Clinical Science  

    Planet Pharma
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    Senior Clinical Science Leader – Alzheimer’s Disease | Global Opportun... Read More
    Senior Clinical Science Leader – Alzheimer’s Disease | Global Opportunity Location : Flexible / Remote options available depending on location We are supporting a leading organisation at the forefront of advancing brain health and cognitive assessment technologies, who are seeking an experienced Senior Clinical Science Leader specialising in Alzheimer’s Disease to join their growing scientific team. This is a unique opportunity for a senior scientific expert to play a key role in shaping clinical trial strategies, supporting global pharmaceutical partners, and advancing approaches to cognitive endpoint management within Alzheimer’s and neurodegenerative disease research. The successful candidate will act as a trusted scientific advisor, partnering with sponsors, clinical teams, and internal stakeholders to provide expertise across endpoint strategy, data quality, cognitive assessments, and rater quality programmes. Key Responsibilities : Provide scientific leadership and consultation across Alzheimer’s Disease clinical trial programmes. Support sponsor discussions, proposal development, and scientific bid presentations. Advise on endpoint strategy, cognitive assessments, and quality management approaches. Develop and implement strategies to support endpoint quality and data integrity. Lead rater training initiatives, including training content development, evaluation criteria, and remediation activities. Support scientific publications, conference presentations, and thought leadership activities. Collaborate cross-functionally with clinical operations, data science, technology, and scientific teams. Build strong relationships with sponsors, clinical experts, and key opinion leaders within the Alzheimer’s research community. About You: PhD or PsyD in Clinical Neuropsychology, Clinical Psychology, or related discipline. Significant experience supporting Alzheimer’s Disease clinical trials (essential). Strong understanding of neurodegenerative disease research and cognitive endpoints. Experience across early and late-stage clinical studies. Expertise in areas such as: Endpoint strategy Cognitive assessments Endpoint quality management Rater training and quality programmes Clinical outcome assessments (COAs) Established scientific credibility through publications, presentations, or thought leadership. Comfortable acting as a scientific partner with pharmaceutical sponsors and external stakeholders. Why consider this opportunity? Work at the forefront of Alzheimer’s Disease research and cognitive science. Influence how clinical trials measure and evaluate cognitive outcomes. Partner with leading pharmaceutical organisations globally. Join a highly collaborative scientific environment where innovation and expertise directly impact future treatments. If you are a Clinical Neuropsychology expert with deep Alzheimer’s clinical trial experience and are looking for a role where you can influence scientific strategy and innovation, I would be keen to connect. Read Less
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  • Clinical Trial Supply Manager  

    Planet Pharma
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    Planet Pharma is seeking a Clinical Trial Supply Manager to join a glo... Read More
    Planet Pharma is seeking a Clinical Trial Supply Manager to join a global clinical supply chain team responsible for ensuring the timely delivery of investigational products for clinical studies worldwide. This role sits within a highly collaborative environment and focuses on the operational execution of clinical trial supply strategies across Phase I-III studies. The successful candidate will manage supply activities from study start-up through close-out, working closely with Clinical Operations, Logistics, Quality, Packaging, Labeling, and external partners to ensure uninterrupted supply to investigational sites and depots globally. Key Responsibilities Develop and maintain clinical supply strategies for assigned clinical studies and compounds. Translate clinical demand forecasts into effective supply plans that ensure uninterrupted product availability. Manage investigational product supply within Interactive Response Technology (IRT) systems. Coordinate packaging, labeling, manufacturing, distribution, and inventory activities to support global clinical trials. Collaborate with cross-functional teams including Clinical Development, Logistics, Quality, Regulatory, Manufacturing, and external vendors. Monitor clinical supply inventories and drug utilization trends, identifying potential risks and mitigation strategies. Support global investigational product distribution strategies at depot and site level. Ensure timely release and delivery of clinical supplies in compliance with country-specific regulatory requirements. Manage expiry tracking, use-date extensions, relabeling activities, and product lifecycle management. Participate in protocol review and provide supply chain input to support study design and operational execution. Identify and drive continuous improvement opportunities across clinical supply chain processes. Lead supply-related discussions in study team meetings and communicate risks, timelines, and mitigation plans. Support inspection readiness activities, documentation management, and compliance requirements. Manage deviations, product complaints, and supply-related issues through to resolution. Required Experience Read Less
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  • Associate Director, Global Regulatory Strategy  

    Planet Pharma
    - Hertfordshire
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    Associate Director, Global Regulatory Strategy (Neurology) 📍 Location:... Read More
    Associate Director, Global Regulatory Strategy (Neurology) 📍 Location: Hatfield, UK (Hybrid – 3 days onsite) 📄 Employment Type: Permanent Are you an experienced Regulatory Affairs professional looking to play a strategic role in shaping the future of innovative neurology therapies? We are partnering with a global pharmaceutical organisation seeking an Associate Director, Global Regulatory Strategy to join its international Regulatory Affairs team. This is a high-impact opportunity to influence global regulatory strategy across both development and marketed products while working alongside senior leaders across Europe, the US, and Japan. This role offers significant visibility within the organisation, the opportunity to represent the company at industry forums and regulatory conferences, and the freedom to help shape future regulatory strategy. The Opportunity As Associate Director, you will take ownership of global and/or European regulatory strategy for a diverse neurology portfolio spanning both development and lifecycle management. You'll work cross-functionally with Clinical Development, Medical Affairs, Commercial, and other key stakeholders to develop innovative regulatory approaches that support successful product development and approvals. This position offers a broad international remit with exposure to multiple markets and the opportunity to contribute to strategic initiatives beyond your core responsibilities. Key Responsibilities Lead global and/or EU regulatory strategies across assigned development and commercial products. Develop and execute regulatory submission strategies for CTAs, MAAs, and post-approval activities. Lead interactions with health authorities, including scientific advice meetings and regulatory discussions. Author and review high-quality regulatory documentation and agency responses. Collaborate with global cross-functional teams to align regulatory strategy with clinical development plans and business objectives. Drive lifecycle management activities for marketed products. Identify regulatory risks and develop proactive mitigation strategies. Represent Regulatory Affairs on cross-functional project teams. Contribute to process improvements and strategic regulatory initiatives across the organisation. What We're Looking For We're interested in speaking with Regulatory Affairs professionals who can demonstrate: Extensive pharmaceutical Regulatory Affairs experience within innovative medicines. Strong experience supporting drug development programmes. Experience developing and executing regulatory strategies. Experience leading or contributing to CTA and MAA submissions. Experience leading interactions with health authorities, particularly within Europe (EMA experience highly desirable). Scientific Advice experience. Strong knowledge of European regulatory requirements. Excellent written and verbal communication skills. Ability to influence senior stakeholders within a global matrix environment. Strategic mindset with strong leadership and decision-making capabilities. Highly Desirable Neurology therapeutic area experience. Experience across both development and established products. Global Regulatory Strategy experience. Experience with Paediatric Investigation Plans (PIPs). Experience representing organisations at industry or regulatory forums. Education Bachelor's degree in Life Sciences or a related scientific discipline. Master's, PharmD or PhD would be advantageous. Working Environment Hybrid working (3 days per week onsite in Hatfield). International collaboration across Europe, the US and Japan. Approximately 20–30% domestic and international travel. Opportunity to work with senior leadership on high-profile development programmes. Why Apply? This is an excellent opportunity to join a highly collaborative global Regulatory Affairs team where you'll have genuine influence over regulatory strategy rather than simply executing submissions. You'll enjoy broad exposure across development and commercial products, meaningful interaction with global health authorities, and the chance to help shape the regulatory direction of innovative medicines in neurology. If you're looking for your next strategic Regulatory Affairs opportunity, we'd love to hear from you. 📩 Apply today or contact me directly for a confidential discussion. Read Less
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  • Global Clinical Program Director  

    Planet Pharma
    - Greater London
    Apply Now
    Summary Exciting opportunity with a global biotech organisation seekin... Read More
    Summary Exciting opportunity with a global biotech organisation seeking an experienced Clinical Operations leader to drive clinical development strategy and execution across the full product lifecycle—from First-in-Human studies through registration and post-marketing activities. This is a highly visible leadership role, combining strategic oversight, operational excellence, and cross-functional collaboration on global development programs. Responsibilities: Lead clinical operations strategy and provide input into global Clinical Development Plans (CDPs) and program objectives. Oversee clinical development activities across assigned indications and ensure delivery against timelines, budgets, and quality expectations. Drive operational risk management, issue resolution, and cross-functional decision-making. Partner with Clinical Trial Leads, Project Managers, and senior stakeholders to ensure successful execution of global clinical programs. Support country and site selection, CRO management, and regulatory readiness activities. Lead and mentor clinical operations teams, fostering a culture of collaboration, innovation, and continuous improvement. Ensure inspection readiness and support audits across the development portfolio. Requirements: 15+ years of experience in Clinical Development and Clinical Operations leadership within biotech or pharmaceutical organisations. Strong background in global clinical trial management, strategic drug development, and operational execution. Proven experience leading complex global programs and working effectively within matrix environments. Experience managing CROs, external partners, and outsourced clinical development models. Strong leadership, stakeholder management, and team development capabilities. Thorough knowledge of ICH-GCP and global clinical development regulations. Degree in Life Sciences, Biomedical Sciences, Pharmacy, Medicine, or a related discipline. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters 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 recognized 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. www.planet-pharma.com TO APPLY Please click ‘apply’ or contact Joesela Alolod A. (Recruitment Sourcer) at Planet Pharma for more information: E: JAnzures@planet-pharma.com T: +61 370580550 Linkedin: www.linkedin.com/in/joeselaaloloda/ Read Less
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  • Chief Data Officer  

    Planet Pharma
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    Chief Data Officer – UK or Poland (Home‑Based) Executive Leadership |... Read More
    Chief Data Officer – UK or Poland (Home‑Based) Executive Leadership | Data Strategy | Enterprise Transformation A leading global life‑sciences organisation is seeking an accomplished Chief Data Officer (CDO) to drive enterprise‑wide data strategy, architecture, and transformation. This is a senior, VP‑level position with responsibility for shaping and delivering the company’s data vision while leading a high‑performing team of Senior/Executive Directors across the UK and US. About the Role The CDO will report directly to the Chief Information Officer and will lead a specialist team of 4–5 senior data leaders. This is a strategic‑technical hybrid role requiring both high‑level vision and hands‑on capability. Candidates must be able to define enterprise data direction while also diving into architecture, tooling, design, and delivery where necessary. This position is home‑based and can be performed from the UK or Poland . Key Responsibilities Define and execute the organisation’s enterprise‑wide data strategy Lead data transformation initiatives across architecture, governance, quality, and operations Oversee creation of data lakes, warehouses, lakehouses, and modern data platforms Drive the transition to Azure‑based cloud environments and modern engineering practices Build an enterprise data model capable of standardising sponsor data received in various formats Develop and implement Medallion Architecture (Bronze/Silver/Gold layers) Guide the ingestion, curation, standardisation, and consumption of data Deliver scalable data solutions that support multi‑tenancy and SaaS offerings Lead innovation and champion data‑driven improvements across the organisation Manage a senior team responsible for data engineering, architecture, governance, and strategy What We’re Looking For Industry Experience (mandatory) Pharma, biotech, healthcare, or broader life‑sciences data leadership Candidates outside these industries will not be considered. Technical Read Less
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  • Remote CDO: Data Strategy & Transformation (UK/Poland)  

    Planet Pharma
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    A leading global life-sciences organization is seeking a Chief Data Of... Read More
    A leading global life-sciences organization is seeking a Chief Data Officer (CDO) to drive enterprise-wide data strategy, architecture, and transformation. This senior position requires expertise in pharma data leadership and a strong understanding of Azure and Medallion Architecture. The CDO will oversee a specialized team and be responsible for innovative data solutions and transformation initiatives, ensuring robust enterprise data models and scalable cloud environments. The role can be home-based from the UK or Poland. #J-18808-Ljbffr Read Less
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