Scientific Writing Jobs in Worcester
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Search results - Scientific Writing Jobs in Worcester
Albion Rye AssociatesWorcester
complex scientific information into clear, accurate, and engaging content.
• Comfort using AI and digital tools as part of the writing and content development process.
• Strong client communication and stakeholder engagement skills.
Education
• Master’s...
The RFT GroupWorcester
Principal Medical Writer, Clinical Development
Our client is a Biotech company with a strong pipeline, now wish to hire a Principal Medical Writer within their Clinical Development team, working closely with functional teams e.g. Clinical...
Meet Life SciencesWorcester
to publication guidelines (GPP, ICMJE, company SOPs).
• Participate in internal review processes to ensure accuracy, consistency, and scientific integrity.
• Contribute to continuous improvement of internal writing processes and best practices.
Skills...
Complete Regulatory | An IPG Health CompanyWorcester
communications solutions for leading pharmaceutical companies worldwide.
What We Do
We specialize in regulatory writing and consultancy services, providing best-in-class support to the pharmaceutical industry. Our work spans a wide range of high-quality...
Cpl Life SciencesWorcester
Job Title: Senior Medical Writer, Clinical and Regulatory
Department: Medical Writing
Location: UK, Fully Remote
Job Type: 12 Month Contract /FTC
Remuneration: Up to £80,000
This is a 12-month contract role, and you MUST be able to start...
The RFT GroupWorcester
Medical Writing Manager
Our client is a Biotech company with a strong pipeline, now wish to hire a Medical Writing Manager working closely with functional teams e.g. Regulatory Affairs, Medical Writing, Clinical Operations, Medical Affairs, etc...
DigiTech ResourcingWorcester
Senior Data Scientist - Experimentation/Causal
Contract Length: 6 months
Rate: £650pd (Inside iR35 if UK based)
Location: Fully Remote
Start: ASAP – ability to deliver impact from Week 1 required
Digitech are partner with a globally recognised...
Planet PharmaWorcester
of scientific experts and medical writers who share a passion for translating complex clinical data into impactful, high-quality publications.
The Opportunity:
We're looking for a Junior Medical Writer and Senior Medical Writer to take a leading role...
Planet PharmaWorcester
and late phase trials.
• Deep understanding of regulatory guidelines (e.g., ICH, EMA, MHRA) and experience with submissions.
• Proficiency in statistical software (e.g., SAS, R) and CDISC standards.
• Excellent communication and scientific writing skills...
VML HEALTHWorcester
and provide expert input to help validate content from both a scientific and technical view point.
Responsibilities:
• Provide expert guidance to a team of medical writers within the field of Ophthalmology or Optometry.
• Act as the 'expert' within...
Mott MacDonaldEnglandappcast.io
The role will require mentoring a team of engineers and scientists, and you will play a key role in their professional development. The role may also include line management responsibility in future.
• Degree in Chemical Engineering or related engineering...
Englandcv-library.co.uk
applications.
Authoring technical reports and assessments (screening & scoping, human health impact, operational technical opinions).
Managing, mentoring and influencing a multidisciplinary team of consultants, scientists, hydrogeologists and sub-contractors...
BioTalentWorcester
quality checks, and literature searches with concise summaries.
• Develop presentations, slides, and posters for scientific meetings.
• Maintain accurate and complete project data and documentation.
• Collaborate with cross-functional teams...
Evidencia Scientific Search and Selection LimitedWorcester
scientific rigour with strategic insight to help pharma and biotech clients achieve real-world market access success. With a collaborative, low-ego culture, low staff turnover, and clear career progression pathways, this is a firm where people genuinely...
Planet PharmaWorcester
and regulatory readiness.
This role is highly hands-on, focused on writing, reviewing, and approving GMP batch documentation, managing Quality System activities (CAPAs, deviations, change controls), and contributing technical and regulatory input for small...
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