Biotechnology Jobs

394 jobs for “Healthcare”

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GSK logo

GSK · 10000+ people · Public

Director, Real-World Evidence & Health Outcomes, mRNA Vaccines

  • Durham, United States
  • US$203,775 – US$339,625 pa
  • Director

Leads the integrated real-world evidence and health outcomes strategy for mRNA influenza vaccines, designing and interpreting US post-marketing vaccine effectiveness studies across late-stage development, launch and post-marketing phases. Partners with clinical development, epidemiology, medical affairs, regulatory, biostatistics and market access teams, and builds collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.

Medicare · EHR · Administrative Claims +1

2 weeks ago
GSK logo

GSK · 10000+ people · Public

Director, Real-World Evidence & Health Outcomes, mRNA Vaccines

  • USA - Pennsylvania - Upper Providence
  • US$203,775 – US$339,625 pa
  • Director

Provides scientific and strategic leadership for real-world evidence supporting GSK's mRNA vaccine portfolio, with a primary focus on influenza. Leads post-marketing vaccine effectiveness studies in the US, translating evidence needs into rigorous study designs and building collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.

Medicare · EHR

2 weeks ago

Johnson & Johnson Innovative Medicine

Integrated Data Analytics and Reporting (IDAR) Student Placement – Clinical and Statistical Programming (C&SP)

  • High Wycombe
  • Entry level
  • Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

3 weeks ago
Roche logo

Roche · 10000+ people · Public

Field Service Engineer - Somerset Area

  • Dorset
  • On-site
  • Mid-level
  • Permanent

Field-based role maintaining, installing and troubleshooting Roche Diagnostics' electro-mechanical, fluidic and electronic medical equipment across the South and South West of England. You will deliver on-site and office-based customer training, support new product launches and grow key accounts, working with the Regional Technical Manager and wider Technical Services team.

Roche Diagnostics

3 weeks ago
Roche logo

Roche · 10000+ people · Public

Field Service Engineer - Somerset Area

  • Somerset

Diagnose, repair and maintain electro-mechanical, fluidic and electronic diagnostic systems across the South and South West England region, covering installations, preventative and corrective maintenance. Deliver on-site and office-based customer training and support new product launches while working with the Regional Technical Manager and wider Technical Services team.

Roche Diagnostics

3 weeks ago
Novartis logo

Novartis

Expert Regulatory Writer

  • London
  • Hybrid
  • £67,900 – £126,100 pa
  • Senior

Lead the authoring of high-complexity regulatory documents and act as Program Writer for complex programmes, overseeing writing strategy, coordination, planning and resourcing. Partner with clinical trial and submission teams, shape data analysis planning, and champion AI tools to improve regulatory writing quality and efficiency.

Artificial Intelligence

3 days ago
Novartis logo

Novartis

Expert Regulatory Writer

  • Home Worker
  • Remote
  • £67,900 – £126,100 pa
  • Senior

Lead the authoring of high-complexity regulatory documents and act as Program Writer for complex programmes, overseeing writing strategy, coordination, planning and resourcing. Provide expert guidance to clinical trial and submission teams, shape data analysis planning, and champion best practices, new technologies and AI tools to improve writing quality and efficiency.

Artificial Intelligence

3 days ago

IQVIA

Senior Statistical Programmer (FSP)

  • Reading
  • Remote
  • Senior
  • Permanent

Senior Statistical Programmer role focused on reviewing and producing submission-ready ADaM datasets, tables, figures, listings and define.xml for clinical trials. Leads complex SAS programming, pooled and exploratory analyses, and ISS/ISE deliverables, working with study teams and statisticians. Requires strong CDISC knowledge and R experience, dedicated to a major pharma client via an FSP partnership.

SAS · R · define.xml

Today

Eurofins

Product Development Trace Analysis Scientist

  • Macclesfield
  • On-site
  • Permanent

Develops, optimises and validates trace analysis methods using LC-MS and Orbitrap technologies to detect and quantify trace-level small molecules in raw materials, intermediates and drug substances. Provides technical expertise on mutagenic impurities and nitrosamines at parts-per-billion levels, performing complex analytical investigations and authoring method development reports and validation protocols. Based at a client pharmaceutical facility, collaborating with multidisciplinary internal and external teams.

LC-MS · Orbitrap · GC-MS +6

2 weeks ago

Eurofins

Analytical Product Development Senior Scientist

  • Macclesfield
  • On-site
  • Senior
  • Permanent

Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop, optimise and validate analytical methods while training colleagues and driving continuous improvement at a client's Macclesfield facility.

HPLC · Karl Fischer · Mass Spectrometry +1

Last week

LGC

Analytical Chemist

  • Guildford
  • Mid-level
  • Permanent

Hands-on laboratory role analysing pharmaceutical samples including APIs, medicines, herbal products and packaging for MHRA Laboratories. Uses HPLC, GC, GC/LC-MS, IR, Raman, UV, dissolution and wet chemistry, with responsibility for drafting reports, validating data, equipment calibration and maintaining an ISO/IEC 17025 quality system. Works within a team of around 30 analytical scientists, independently coordinating project workloads.

Microsoft Word · Microsoft Excel

4 days ago

Vertex Pharmaceuticals

Vertex Summer Intern, Health Economics & Outcomes Research (10 weeks)

  • London
  • Hybrid
  • Entry level
  • Internship

A 10-week summer internship supporting health economics, real-world evidence and outcomes research projects that inform value-based decision-making and evidence generation. Interns work with large databases and spreadsheets, collaborate with industry teams, and present findings, gaining hands-on biopharma experience.

Excel · PowerPoint · MS Office

Yesterday

IQVIA

Clinical Monitoring Analyst (Cluepoints)

  • London
  • Remote
  • Lead

Supports the Centralized Monitoring Lead in building study-specific monitoring strategies, programming quality tolerance limits, key risk indicators and data visualisations on the Cluepoints platform. Handles platform setup, scheduled refreshes, specification documents and peer reviews, working directly with a sponsor on a dedicated project. Requires strong SAS macro skills and prior data management experience.

Cluepoints · SAS · EDC Systems +1

2 days ago

Ipsen

Senior Medical Director, Neurosciences, Asset Medical Lead

  • London
  • Hybrid
  • Director · manages people

Leads global medical strategy for the Neurosciences portfolio, primarily Dysport Movement Disorders indications, defining evidence generation plans, registries and investigator-sponsored research. Acts as Medical functional lead on the global Asset Team, chairs the Medical & Evidence Generation Team, and represents Ipsen with KOLs, societies and advocacy groups. Also leads, coaches and develops Global Medical Directors across the organisation.

Dysport

Last week

Parexel

Clinical Trial Manager, (Oncology Experience Required)

  • London
  • Remote
  • Mid-level · manages people

Lead local study delivery for a single client's oncology trials, overseeing operational execution, budgets, and compliance with ICH-GCP and local regulations. Manage Local Study Teams, regulatory and ethics submissions, and country-level financial agreements. Remote UK role in a fast-paced clinical research environment.

Study Financial Systems

2 days ago

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