26 to 50 of 278 Remote Pharmaceutical Jobs

global healthcare agency specialising in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry's most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organisations. Our mission is to be a community of the very best people, building trusted partnerships across the healthcare More ❯

About NTT DATA Business Solutions: NTT DATA Business Solutions Group is part of the NTT DATA Corporate Group a top 10 global IT services provider, headquartered in Tokyo, operating in more than 50 countries. We combine a global reach with More ❯

About NTT DATA Business Solutions: NTT DATA Business Solutions Group is part of the NTT DATA Corporate Group a top 10 global IT services provider, headquartered in Tokyo, operating in more than 50 countries. We combine a global reach with More ❯

Senior Data Analyst – RWE | Global CRO – Client FSP | UK & Europe | Home based | We’re hiring a Senior Data Analyst to join our clients expanding Real-World Evidence team where you will be fully embedded within our client’s FSP model More ❯

Who we are We are a London tech startup on the lookout for bright, motivated and self-driven individuals to join the team. Who you are You are a recent PhD graduate, or about to graduate, in a STEM field More ❯

in ensuring compliance with critical international standards and regulations across a rapidly expanding platform. As a Compliance Manager for the EMEA region, you'll lead efforts to support regulated pharma environments, manage internal and external audits, and influence the company's quality strategy in collaboration with technical and customer-facing teams. If you are experienced in GxP, ISO, and EU … sales cycles and customer engagements. Maintain comprehensive documentation and drive cross-functional consistency across regulatory processes. 10+ years of experience in software lifecycle management and validation, with emphasis on pharma or biotech compliance. Solid knowledge of EU regulatory frameworks (e.g., GxP, 21 CFR Part 11, Annex 11). Experience preparing for and navigating ISO, SOC, and other third-party compliance … s degree in computer science, life sciences, or a related field. Preferred: Advanced degree in compliance or regulatory affairs; ISO 9001 Lead Auditor certification; experience working with EU-based pharmaceutical companies. Competitive salary and equity in a high-growth organization. Remote-first culture with flexible working arrangements across EMEA. Generous paid time off (PTO) to support work-life balance. A More ❯

global institutions. Our comprehensive in-house capabilities assist partners in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National … join the Company and support our expanding business and scientific efforts. The selected candidates will be responsible for developing and fostering relationships with key decision-makers at Biotech and Pharmaceutical companies and Not-For-Profit Organizations to secure business opportunities for the Company. The successful candidates will be self-motivated, success-driven individuals who are well networked within the life … related field required Working knowledge of drug discovery Fluent in English (both written and oral) 5+ years of business development/sales experience in life sciences/biotech/pharma Proven sales track record in life sciences industry - a preference will be given to a track record of sales in the drug discovery arena. A strong network of senior level More ❯

protocols and study reports Education & Experience Qualifications Advanced degree, including PhD in Epidemiology, population health, outcomes research, or a related discipline and 7+ years of relevant experience in the pharmaceutical, academic and/or medical environments (at least 3 of which need to be at a pharmaceutical company or partnering with pharmaceutical companies); or, MPH or another relevant Master's … study reports Education & Experience Qualifications Minimum Requirements: Advanced degree, including PhD in Epidemiology, population health, outcomes research, or a related discipline and 7+ years of relevant experience in the pharmaceutical, academic and/or medical environments (at least 3 of which need to be at a pharmaceutical company or partnering with pharmaceutical companies); or, MPH or another relevant Master's More ❯

take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology, and consulting to cater to the unique needs of small, medium, and large pharmaceutical companies. Job Title: Consulting Technology Programme Manager (PV Systems) Job Type : Full-Time Job Description: Programme Manager will be responsible for the successful orchestration of interrelated projects that together deliver … to deliver program outcomes on time, within budget, and to high quality standards. They must be highly experienced, strategic thinker with deep domain expertise in software delivery for the pharmaceutical industry—particularly in the areas of pharmacovigilance, safety, and regulatory technology. Key Responsibilities: Define, lead, and manage the successful execution of complex, multi-workstream programmes for pharmaceutical clients. Align programme … Master's degree in Computer Science, Information Technology, Project Management, or a related field. 12+ years of experience in client facing project and programme management delivering software solutions to pharmaceutical or life sciences clients. Excellent leadership, strategic thinking, and stakeholder management skills. Proven ability to manage crossfunctional, geographically distributed teams and external vendors in a matrixed environment. Knowledge of regulatory More ❯

1. To support the implementation of the EPMA products within UHBW designated areas, working collaboratively with clinical and digital teams. 2. To provide specialist advice and practical input regarding pharmaceutical aspects of a wide range of therapeutic treatments, supporting clinicians, healthcare staff, and managers to promote safe and compliant electronic prescribing and digital medicines practice. 3. Contribute to clinical governance … responsibilities For a more detailed job description and main responsibilities, please refer to the job description document attached to this vacancy. Person Specification Qualifications and Training Registration with General Pharmaceutical Council. Postgraduate Diploma or equivalent in Clinical Pharmacy Evidence of continuing professional development. Additional postgraduate qualifications relating e.g. leadership/management, research, digital health, education and training Membership of the … British Computer Society. Membership of the Royal Pharmaceutical Society of Great Britain. Knowledge and Experience Experience in supporting change management and/implementing large change projects in the NHS Experience of working with senior healthcare professionals outside of Pharmacy to achieve Trust wide developments. Experience of supervising others, including for research and audit projects Experience of practice research or audit More ❯

the job 1.To support the implementation of the EPMA products within UHBW designated areas, working collaboratively with clinical and digital teams. 2.To provide specialist advice and practical input regarding pharmaceutical aspects of a wide range of therapeutic treatments, supporting clinicians, healthcare staff, and managers to promote safe and compliant electronic prescribing and digital medicines practice. 3.Contribute to clinical governance activities … responsibilities For a more detailed job description and main responsibilities, please refer to the job description document attached to this vacancy. Person specification Qualifications and Training Registration with General Pharmaceutical Council. Postgraduate Diploma or equivalent in Clinical Pharmacy Evidence of continuing professional development. Additional postgraduate qualifications relating e.g. leadership/management, research, digital health, education and training Membership of the … British Computer Society. Membership of the Royal Pharmaceutical Society of Great Britain. Knowledge and Experience Experience in supporting change management and/implementing large change projects in the NHS Experience of working with senior healthcare professionals outside of Pharmacy to achieve Trust wide developments. Experience of supervising others, including for research and audit projects Experience of practice research or audit More ❯

global experience. We are in search of a Technical Event Project Manager to join our team to ensure the successful project management and delivery of exhibition booths for our Pharmaceutical Clients. About the Technical Event Project Manager As the Technical Event Project Manager, you will have experience in the design and project management of exhibition booths with a keen eye … Event Project Manager for your technical expertise in the end-to-end production of exhibition booths in the life sciences industry. You will have worked with a variety of Pharmaceutical Clients and will have utilized your creative and technical skills to support the design and build of exhibition booths in congress halls across Europe. You will be proficient at working More ❯

global experience. We are in search of a Technical Event Project Manager to join our team to ensure the successful project management and delivery of exhibition booths for our Pharmaceutical Clients. About the Technical Event Project Manager As the Technical Event Project Manager, you will have experience in the design and project management of exhibition booths with a keen eye … Event Project Manager for your technical expertise in the end-to-end production of exhibition booths in the life sciences industry. You will have worked with a variety of Pharmaceutical Clients and will have utilized your creative and technical skills to support the design and build of exhibition booths in congress halls across Europe. You will be proficient at working More ❯

Veeva Business Consulting group in R&D, a priority area for Veeva. We work with senior customer stakeholders, as the partner of choice for 85% of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance). As a Senior Consultant, you will manage … Master's degree and excellent academic record 4+ years consulting experience in an established strategic/management consulting organization Experience in Life Sciences Good understanding and deep interest in pharmaceutical R&D, having delivered consulting engagements in one or more of the following areas: Regulatory, Clinical, Quality, Safety Good understanding of the R&D value chain and ideally Veeva's More ❯

Education, experience and qualifications 1-4 years of experience in a Cloud Engineering or DevOps role. Relevant training and/or certifications as a Cloud Engineer Experience in the pharmaceutical or regulated industry Demonstrated experience with deploying services and platforms in AWS cloud, Microsoft Azure, AI, Databricks, Microsoft Fabric, Demonstrated experience in transitioning from project mode to operations and support More ❯

Data Protection Laws Compliance (e.g., GDPR, ePrivacy, DGA, EHDS, NIS 2) Experience in the Life Science industry, including in-house or external legal, compliance, operational or consulting roles supporting pharma, biotech, med-tech, and/or clinical research organizations is nice to have Experience on privacy by Design & Default Implementation and risk assessments in collaboration with operational, IT, IT Security More ❯

Deep knowledge of Industry’s QA and QC processes alongside all QM elements in one or more of the following sectors is an advantage: Aerospace and Defence, Consumer Products, Pharma or Discrete Manufacturing. Leadership experience across small to medium-sized teams, both onshore and offshore Commitment, flexibility, thought leadership and a hunger to develop your career within the SAP SCM More ❯

Deep knowledge of Industry’s QA and QC processes alongside all QM elements in one or more of the following sectors is an advantage: Aerospace and Defence, Consumer Products, Pharma or Discrete Manufacturing. Leadership experience across small to medium-sized teams, both onshore and offshore Commitment, flexibility, thought leadership and a hunger to develop your career within the SAP SCM More ❯

is looking for a Migration Architect who will become a leading member of our EU Professional Services group, providing migration solutions on project teams implementing Veeva Vault R&D (pharmaceutical development) applications and Vault Platform cloud solutions to companies in the Life Sciences industry. You will lead customer migration implementations by providing expertise with data and document content migration, Vault More ❯

a differentiated consulting service in Life Sciences with a compelling value proposition - building on Veeva's position as the digital partner of choice for 85% of the top 20 Pharmaceutical companies. As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers - managing teams and planning, organizing, and tracking all aspects of delivery. You will analyze More ❯

Spherical Search have partnered up with a well-known Analytical Services/CRO company who specialise in the inhalation and nasal drug delivery space , working with a range of pharmaceutical companies and drug delivery device developers. My client is currently looking for a Project Manager to work at their Cwmbran site. This would be a hybrid role with the option More ❯

of artificial intelligence (AI), to enhance efficiency, effectiveness, and service delivery. You will be working with a variety of clients which may include Sponsors of Clinical Trials, research organisations, pharmaceutical manufacturing organisations, Clinical research organisations, MedTech and Biotech companies. Our services are delivered based on a balance of working remotely from home and occasional visits to clients at their offices. More ❯

About ZAVA We're on a mission to provide our patients with healthcare that is accessible and dependable at a fraction of today's cost. Our team of Doctors, Engineers, Customer Support Advisors, Marketers, Product Managers, UX Designers, Pharmacists, and More ❯

Who we are We are a London tech startup on the lookout for bright, motivated and self-driven individuals to join the team. Who you are You are a DevOps/Site Reliability Engineer with experience managing complex infrastructure and More ❯

you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing … dedicated to reshaping the future of healthcare. Additional Benefits: Home-based remote work opportunities Great work/life balance Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors Cohesive team environment fostering a collaborative approach to study work Variety of therapeutic areas, indications and, study phases Job stability; long-term engagements and development opportunities Career … Science, Mathematics, Statistics or related area with relevant experience Experience • At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. • Indepth understanding of clinical programming and/or statistical programming processes and standards. • Indepth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). More ❯