1 to 25 of 40 Biotechnology Jobs in the UK with Remote Work Options

I suggest making an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery recruitment specialists, Newton Colmore, on (phone number removed) or submit an application, and a member of our team at Newton Colmore will more »

shows and events. Investigate new applications and sales potentials. Collect and report market information to the organization. Your profile B.Sc. in Sciences, preferably biology, biotechnology, chemistry or pharmacy. M.Sc. or PhD a plus. New starters in sales welcome, sales experience in laboratory equipment a plus. Commercially driven, technically knowledgeable and more »

Mantell Associates is an industry backed, multidiscipline global Life Science and Pharmaceutical headhunting firm focused on providing staffing solutions, in particular to the Biotech, Pharmaceutical, Large Molecule, Cell & Gene Therapy, CRO & Clinical Operations, Small Molecule, and Life Science Consulting sectors with our headquarters based in the City of London, and more »

Job Title: Senior Bioinformatician Location: United Kingdom - Hybrid I'm partnered with an exciting Discovery stage Biotech whose pipeline consists of Oncology & Fibrosis indications! They boast an impressive ECM platform and team rich in experience and an ambitious mindset! Job Description: The role is for a Senior Bioinformatician whose well more »

HR...Who? We are the market research partner of choice for healthcare, pharma and biotech businesses seeking a competitive edge, through scientifically grounded methodologies and perceptive insight. Not only do we work with world renowned giants of the healthcare industry, but we also partner with up and coming organisations. Whichever the more »

data-driven culture. Principal Computational Biologist Qualifications & Experience: Required – PhD in computational biology or related PhD – Experience delivering results in a fast-paced environment (biotech/pharma exposure would be an advantage) – Strong experience in developing and modifying statistical (and ML) models of ‘omics datasets for biological interpretation and actionable more »

to foster a data-driven culture. Qualifications & Experience Required PhD in computational biology or related Experience in delivering results in a fast-paced environment (biotech/pharma industries would be a distinct advantage) Strong experience in developing and modifying statistical (and ML) models of ‘omics datasets for biological interpretation and more »

related field, such as pharmaceutics; chemistry or biology preferred. Experience Previous experience within the life sciences industry, with preferred experience in the pharmaceutical and biotech industry including cell and gene therapy or clinical supply chain. Previous experience with cold storage, logistics or supply chain from outside life sciences industry will more »

Director, Clinical Research Physician (CNS) Our client is a Biotech company with a focus on neuroscience drug development with early-stage and late-stage clinical studies, now have approval for a Director, Clinical Research Physician role working within the Clinical Science team. This hire will work closely with a multidisciplinary … is preferred. 5+ years of relevant clinical research/clinical development experience across broad therapy areas, working to ICH/GCP guidelines in the biotech or pharmaceutical industry, or clinical setting is preferred. Experience in contributing to clinical study design, clinical protocol development, clinical reports, etc. Medical monitoring, and safety … on +353 1 – 2302400/larry@rftgroup.ie The RFT Group , BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie Follow us on Twitter, Facebook and LinkedIn more »

company. Experience with C# or Python is required on the back-end, plus React or Angular on the front-end. We need people with BioTech, Life Sciences, or Pharma industry experience, as you will be building a cutting-edge HealthTech project. Within a few months, you will also be mentoring more »

into amazing user experiences. You’ll be based remotely, or in our Sandwich office. At YPrime, we help our clients in the pharma and biotech industries to collect data from patients using mobile devices, assign patients to study treatment groups and dispense clinical trial drugs and supplies using web apps. more »

tight deadlines. What you should have: Up to 7 years of experience in digital/social media, with some of this served in health, biotech, or pharmaceutical media sectors. Agency experience required. College degree (BA or equivalent). A relevant concentration such as Marketing, Communications, Science, or a master's … PowerPoint and Excel Comprehensive understanding of the primary regulatory bodies (such as ABPI, PMCPA, FDA, and FTC) and the social media guidelines that govern biotech and pharmaceutical clients. Ability to grow digital and social media business (with current social, PR or marketing clients) and participate in new business pitches. Working more »

position) Location: UK (remote based) Reports into: SVP Head of Development Operations Apsida Life Science are currently partnered with a growing 300 headcount SME Biotechnology that are looking to appoint a freelance Medical Director/VP to facilitate an IND submittal by EOY. Specific details about the companies technology, products … reach out to Jamie Salmon from Apsida Life Science. Jamie.salmon@apsida.com www.apsida.co.uk Example of Jamie Salmon's Completed Assignments (Contingent & Retained): - Chief Medical Officer - Biotechnology - Oncology - USA - Chief Medical Officer - Biotechnology - Oncology - USA (Freelance) - Chief Medical Officer - Biotechnology - Oncology - UK - Chief Medical Officer - Biotechnology - Oncology - Switzerland - VP Clinical Development & Translational … Medicine - AI Pharma Tech - UK - VP Clinical Development - Biotechnology - Oncology - Germany - Head of Clinical Development - Biotechnology - Oncology - Germany - Senior Director, Clinical Development - Biotechnology - Oncology - UK - Director, Clinical Operations - Biotechnology - Oncology - USA - Director, Clinical Operations - Biotechnology - Oncology - Switzerland - Associate Director, Clinical Scientist - Biotechnology - Oncology - Switzerland Apsida Life Science is a specialist more »

across the business Report up to senior leadership and represent QA in reporting What you will bring: Previous project management experience within pharma/biotech or similar Outstanding knowledge of GCP, TFA and FDA regulations Strong project management principles, key knowledge of agile methodology A desire to be hands-on more »

need to succeed To be considered for the role of Quality Manager, you will need to have demonstrated strategic QA leadership experience within a biotechnology, scientific or laboratory setting.Other key deliverables include: A proven track record of successfully designing and implementing a QMS within a Life Science Research environment, pharma more »

lead and influence internal and external stakeholders in a matrix organisation in industries like FMCG/Food & Beverages/Consultancies, Healthcare/Pharma/Biotech/Nutraceuticals/Medical devices or key Packaging organisations. Commercially aware and able to manage cost and value of projects. Excellent inter-personal skills and more »

or developing client relationships. Experience advising senior leadership within client organizations (e.g., CEO, CSO, COO). Strong understanding of the challenges faced by smaller biotech companies in early development (Proof of Concept to Phase 2). Ability to tailor advice to client constraints, navigating regulatory requirements to streamline development activities. more »

the whole industry. A business-to-business membership organization, we are proud to work with many of the world's leading biopharma, biomanufacturing and biotech companies to share knowledge and best practice, discuss emerging trends and challenges, and drive innovation to influence the future. Since our inception in 2004, we more »

with the wider IGES Group , the vision of the company is to provide a full service from strategy to submission for the pharmaceutical and biotech sector. As such the consultant has a vital role to lead client engagements through excellent communication, project management, and presentation skills. Besides, the consultant will … Primary Responsibility: project delivery and Business Development activities in the Market Access space for existing and new named UK-local accounts of pharmaceutical and Biotech companies, working closely with the Director, and colleagues with delivery expertise in other functional areas and work closely with the Director on Business Development. responsibility more »

Trial Master File Expert Our client is a young innovative clinical stage Biotech company with a strong development pipeline, now have approval for a new position for a Trial Master File (TMF) Expert within the Clinical Development and Operations group. There is flexibility for this hire to work remotely/… for Lead Trial Master File Expert: Bachelor of Science degree is preferred. 10+ years’ experience managing TMFs in Clinical Operations environment, in the pharmaceutical, biotech or CRO industry working ICH/GCP guidelines. Experience in both paper and electronic TMF, and familiarity with naming and filing conventions and the CDISC … on +353 1 – 2302400/larry@rftgroup.ie The RFT Group , BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie Follow us on Twitter, Facebook and LinkedIn more »

private equity backed businesses and privately owned companies. We recruit across all sectors and have particularly strong client relationships in media, retail, pharma/biotech, technology, property/real estate, leisure and business services. Headquartered in London, we have additional offices in continental Europe. For more information, please see the more »

create IP opportunities for the portfolio Requirements Minimum 8 to 10 years’ experience as a drug project manager in a pharmaceutical and/or biotech company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late stage inclusive of GMP more »

. Excellent SAS programming skills (BASE, MACRO, GRAPH). Excellent knowledge of CDISC standards. Statistical Programming experience within a CRO Pharmaceutical/Healthcare/Biotechnology industries. Experience in statistical programming initiatives, and development of processes. Knowledge and experience in database design and structures. The ability to perform all duties as more »

on-scope, and on-budget, and maintain stakeholder alignment throughout the project. Must have the following experience: Extensive experience in managing projects within the biotech or pharmaceutical industry. Solid IT experience running high performing environments in multiple technical and business domains. Excellent communication and interpersonal skills with success in influencing more »

Job Description: Join us in creating and deploying next generation MES solutions using the Tulip (https://tulip.co/) platform for Pharmaceutical and Biotech customers. This is groundbreaking work, reinventing the MES concept. So, as well as knowledge and experience of MES and GxP IT projects, you absolutely must more »