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The position will play a critical part in the Marketing department, overseeing all aspects of the conference lifecycle—from concept development to outreach, logistics, promotion and post-event analysis in support of Marketing and Business Development (BD). Global Marketing Conference Manager. Mana

IT Project Manager Salary: Negotiable Hybrid – Hatfield Key Skills: Pharmaceutical experience The IT Project Manager is responsible for planning, executing, and finalising projects according to scope, deadlines and within budget. The IT Project Manager will also define the project’s objectives and oversee the delivery quality throughout its life cycle, with a strong emphasis on stakeholder management and effective communication with senior managers and directors. What are we looking for? • Experience delivering business changes or IT business system projects to GxP environment, either in a pharma site or equivalent a must have, • Demonstrated experience in IT Project Management., • Demonstrated experience in stakeholder management and presenting to senior managers and directors., • Experience in highly regulated environments such as pharmaceuticals, healthcare, aerospace, or energy would be beneficial., • Has worked in PMO governance environments would be beneficial. What we offer in return • Hybrid working (Depending on role), • Car/Car Allowance (Depending on role), • Electric charging points for Electric/Hybrid vehicles, • Discretionary Bonus, • Free onsite parking, • Subsidised onsite restaurant and coffee shop, • Learning and development opportunities, • Retail discounts If you are interested please apply or send your CV to

We're Hiring: Business System Analyst.

We’re seeking a Safety & Compliance Manager to join a leading research organisation and drive a strong culture of health, safety, and compliance. Act as Biological Safety Officer (BSO) and lead on biosafety matters. Promote a positive safety culture across research and operational teams.

Associate Director, Global Regulatory Strategy 📍 Hertfordshire, UK (Hybrid: 3 days office-based) | 🌍 Global Role | 💼 Permanent Are you ready to shape global regulatory strategies for innovative therapies in neurology? We’re seeking an Associate Director, Global Regulatory Strategy to join a collaborative clinical research and innovation team supporting the development and lifecycle management of our neurology portfolio. In this influential role, you’ll lead or support regulatory strategy across multiple regions, ensuring successful submissions, compliance, and long-term product success. You’ll also contribute to early-stage innovation activities — assessing external platforms, technologies, and assets from a regulatory perspective to inform strategic investment and partnership decisions. You’ll work closely with global colleagues across the UK, US, and Japan to drive regulatory excellence and deliver meaningful outcomes for patients worldwide. What you’ll do • Lead Regulatory Strategy: Develop and implement global and regional regulatory strategies supporting clinical development and marketed products., • Regulatory Due Diligence: Provide regulatory insight during due diligence activities for new platforms, technologies, and in-licensing opportunities, identifying potential risks, opportunities, and pathways to approval., • Manage Submissions: Oversee preparation, review, and delivery of high-quality regulatory submissions (CTA/MAA) in alignment with timelines and business priorities., • Regulatory Authority Interaction: Serve as the primary contact with European health authorities (EMA, MHRA, etc.), leading meetings and authoring Scientific Advice requests., • Lifecycle Management: Drive post-approval activities and product lifecycle strategies to ensure continued compliance and access., • Collaboration & Compliance: Partner with cross-functional teams to ensure regulatory standards, ethical behavior, and compliance with applicable laws and guidelines., • Innovation Support: Work within the innovation team to scope new assets and contribute regulatory perspectives to early clinical or preclinical development planning. What you’ll bring • A degree in Life Sciences (Master’s, PharmD or PhD preferred) with significant regulatory and pharmaceutical experience., • Proven track record developing and executing global regulatory strategies and leading submission activities., • Hands-on experience interacting with European health authorities, including Scientific Advice and Paediatric Investigational Plans., • Demonstrated experience in regulatory due diligence for new assets or business development opportunities., • Strong leadership within matrixed, cross-functional environments, with excellent communication and strategic thinking skills. Why join us You’ll join a high-performing, inclusive team dedicated to advancing neuroscience innovation. We value diverse perspectives and empower our people to contribute their expertise, learn continuously, and make a tangible difference in global patient health. Tshering Sherpa

We’re seeking an experienced Safety and Compliance Manager to lead on all aspects of health, safety, and regulatory compliance within a scientific research environment. This role plays a key part in ensuring the organisation operates to the highest standards of safety, supporting scientific teams and leadership through proactive risk management and expert guidance. Key Responsibilities • Ensure compliance with all relevant health, safety, and regulatory frameworks, including requirements from the Health and Safety Executive, Human Tissue Authority, and Home Office., • Act as the organisation’s appointed Biological Safety Officer, providing expert advice on biological safety, GMO risk assessments, and containment practices., • Develop, implement, and maintain robust health and safety management systems, including policies, SOPs, and risk assessments., • Monitor and promote a positive safety culture across all sites, providing leadership and support to teams on best practice., • Manage safety audits, inspections, and incident investigations, reporting on safety metrics and continuous improvement initiatives., • Maintain compliance calendars, legal registers, and documentation to ensure timely reviews, renewals, and submissions., • Represent the organisation in interactions with regulators, inspectors, and external stakeholders., • Deliver engaging training programmes and communications to raise awareness of safety responsibilities across the organisation. Skills and Experience • Proven experience in health and safety compliance within a scientific, pharmaceutical, or biotechnology environment., • Strong knowledge of health and safety legislation and practical experience in applying it to laboratory operations., • Experience with Biological Safety Officer (BSO) responsibilities and regulatory bodies such as the HTA and Home Office., • Confident in conducting audits, inspections, and developing training materials., • Excellent organisational, communication, and problem-solving skills., • Ability to work autonomously, with a proactive approach to identifying and resolving safety challenges. Qualifications • NEBOSH Diploma (or equivalent) and Grad/Tech IOSH status, • Recent Biological Safety Officer (BSO) qualification Please click ‘apply’ or contact David Rowland (Recruiter II) at Planet Pharma for more information: E: T: +44 20 3928 8381 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.

The company is currently in a phase of rapid growth and to support this growth, is seeking a Business Partner to support the Managed Access Program division, TannerMAP, in driving program implementation, generating new business, and managing day-to-day operations of the division. Tanner Pharma offer

The Pharma Product Development (PD) Global Clinical Operations (PDG) team is committed to realizing Roche’s bold ambition of delivering 20 transformative medicines by 2029. Joining our Clinical Operations Excellence group means youll be a key driver in enhancing the speed and efficiency of clini

Why Roche : What is your key motivation for applying for this placement?. This position is located in Pharma Biosample Services (PBS), a department within the PD (Pharma Development) organization of Roche. During the placement you will be based in the Roche UK offices at the Welwyn Garden City site.

The PositionThe Opportunity:Roche is seeking an intern who is pursuing an undergraduate degree with an interest inQuantitative Clinical Pharmacologyin the Pharmaceutical Industry. Our interns will join the Predictive Modelling chapter within the Pharma Research and Early Development (pRED)

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Please click ‘apply’ or contact Finlay Keyworth at Planet Pharma for more information:. Medical Scien

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

They are looking to significantly ramp up and grow their consulting presence in the Global Pharmaceutical, Bio Tech and Life Sciences sector and as such are looking for a number of Senior Managers to join the team focussed on strategy & delivery across the Customer (Sales, Marketing, N. They are loo

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Please click ‘apply’ or contact Finlay Keyworth at Planet Pharma for more information:. Proven experi

This lovely agency are going from strength to strength delivering global high profile events for a range of pharma and healthcare clients. We are seeking a driven and experienced Senior Event Project Manager with a strong understanding of the pharmaceutical compliance regulations and large scale log

Medical Information plays a crucial role in promoting the safe and effective use of healthcare products, supporting healthcare professionals in their clinical decision-making, and helping pharmaceutical and biotech companies meet regulatory compliance standards. Planet Pharma is an American parented

Access to projects for major global clients in tech, pharma, and beyond. Customers include 90 of the globe’s top 100 brands, the top 10 pharmaceutical companies and 18 of the top 20 patent filers worldwide. Our client base spans Europe, Asia Pacific, and North and South America across the technolo

We're partnering with a leading global biopharma company to find an exceptional. Interested? Apply now for immediate consideration or contact Michael Owusu-Ansah on +44 203 928 6631 – mowusu-ansah@planet-pharma. Planet Pharma is an Employment Business providing Global Staffing services.

Access to projects for major global clients in tech, pharma, and beyond. Customers include 90 of the globe’s top 100 brands, the top 10 pharmaceutical companies and 18 of the top 20 patent filers worldwide. Our client base spans Europe, Asia Pacific, and North and South America across the technolo

Identify and technically evaluate new product and technology opportunities, primarily in the oncology and radiopharmaceutical space. 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

Role: -QA Manager-Pharma Biotech (Sterile) Location: -Alderley Edge - onsite onlySalary: - Competitive salary (DOE)Hours: Days (Monday - Friday) 40 hours per weekBenefits: 25 days holiday + BH, private medical care, share options scheme &company pension Russell Taylor Group have a fantastic opportun

Planet Pharma is looking for a. Proven experience in lab management within a pharma, biotech, or industrial setting.

Knowledge of NHS pharmaceutical tenders and contracting procedures. Demonstrable experience launching new pharmaceutical products into NHS hospitals. Specialist Nurses & Pharmacists.

A degree in Life Sciences (Master’s, PharmD or PhD preferred) with significant regulatory and pharmaceutical experience.

Hobson Prior is seeking a Principal Statistical Programmer to join a global team supporting oncology-focused projects.This role involves working on advanced clinical trials (Phase II-III) and contributing to the development of statistical programming outputs.You will play a key role in designing dat

Lab management experience in pharma/biotech. 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 extensive functional expertise including: Regulatory

Hobson Prior is seeking a Principal Statistical Programmer to join a global team supporting oncology-focused projects.This role involves working on advanced clinical trials (Phase II-III) and contributing to the development of statistical programming outputs.You will play a key role in designing dat

A leading global biopharmaceutical company with one of the industry’s most diverse and promising pipelines is seeking an experienced. Strong background in the pharmaceutical/biotech industry with significant clinical supply chain management experience (global scope preferred). If this role isn’t

Hobson Prior is seeking a Principal Statistical Programmer to join a global team supporting oncology-focused projects.This role involves working on advanced clinical trials (Phase II-III) and contributing to the development of statistical programming outputs.You will play a key role in designing dat

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Hobson Prior is seeking a Principal Statistical Programmer to join a global team supporting oncology-focused projects.This role involves working on advanced clinical trials (Phase II-III) and contributing to the development of statistical programming outputs.You will play a key role in designing dat

Cardiology Application Specialist – Nuclear Medicine & PET.Are you passionate about advancing cardiac imaging and supporting innovation in Nuclear Medicine? We’re looking for a Cardiology Application Specialist to join our client's growing team dedicated to delivering world-class clinical and te

Hobson Prior is seeking a Principal Statistical Programmer to join a global team supporting oncology-focused projects.This role involves working on advanced clinical trials (Phase II-III) and contributing to the development of statistical programming outputs.You will play a key role in designing dat

We are seeking a highly experienced and strategic Director of Biostatistics to lead statistical activities across a portfolio of oncology clinical trials, spanning early to late phase development.This is a senior individual contributor role, ideal for someone who thrives in a hands-on, scientificall

Through strong interaction at a senior management level within Tanner Pharma and major biopharmaceutical companies, this is an ideal role for a candidate seeking a robust development opportunity that can be parlayed into a general management career path in the life sciences industry. Founded in 2002

Proven experience in health and safety compliance within a scientific, pharmaceutical, or biotechnology environment. Please click ‘apply’ or contact David Rowland (Recruiter II) at Planet Pharma for more information:. Planet Pharma is an American parented Employment Business/Agency that provides

Join a leading global pharmaceutical company at the forefront of innovation in critical care. Proven success in pharmaceutical sales, particularly within hospital and healthcare settings. Knowledge of NHS pharmaceutical tenders and contracting procedures.

Associate Director, Technology Evaluation – Radiopharmaceutical Innovation. Reporting to the VP, Innovation & Strategy, this role will lead the identification, scientific assessment, and strategic evaluation of new radiopharmaceutical opportunities, with a focus on oncology. Scout, evaluate, and p

Origin Pharmaceutical Packaging are Pharma Packaging specialists who facilitate their clients success through a complete offering from design through product development, regulatory approval, testing, production, and managed supply.

Clarity Pharma Ltd is a leading Pharmaceutical Wholesaler and Third Party Logistics Service Provider. Founded since 1999, we have had huge success over the years, winning numerous awards including the 'Alantra Pharma Fast 50' award for two years running.

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

Our client is a global leading and highly innovative biopharmaceutical services company, one that has enjoyed many years of unprecedented success.

OverviewWe are seeking a highly experienced and strategic Director of Biostatistics to lead statistical activities across a portfolio of oncology clinical trials, spanning early to late phase development.This is a senior individual contributor role, id

Tanner Pharma offers its biopharmaceutical partners a portfolio of four distinct service offerings that span the product lifecycle from clinical development to commercialization. Founded in 2002, Tanner Pharma Group is a specialty service provider in the biopharmaceutical industry focused on improvi

OverviewWe are seeking a highly experienced and strategic Director of Biostatistics to lead statistical activities across a portfolio of oncology clinical trials, spanning early to late phase development.This is a senior individual contributor role, id

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 extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissio

OverviewWe are seeking a highly experienced and strategic Director of Biostatistics to lead statistical activities across a portfolio of oncology clinical trials, spanning early to late phase development.This is a senior individual contributor role, id

Executive Director, Health Economics and Outcomes Research (HEOR), EU / USA.Your chance to join the most innovative, forward thinking and flexible global CRO.Do you wish to play a key role in shaping the direction of a first in class Late Phase business?.Do you bring a high level of credibility and