Medical Writer
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Job Location:
Greater London - UK
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Medical Writer Oncology Central London
Were looking for an experienced Medical Writer to join a growing drug development company based in central London focused on advancing innovative oncology treatments.
This is an exciting opportunity to be part of a small agile and collaborative team working across five oncology assets in pre-clinical and early-phase development. Youll work closely with cross-functional experts reporting to the Senior Clinical Scientist to create review and edit high-quality regulatory and scientific documentation that supports the companys development pipeline.
Key Responsibilities:
#MedicalWriter #ClinicalScience #ScientificWriting #Oncology #CancerResearch #OncologyJobs #EarlyClinicalDevelopment #ClinicalTrials #Biotechnology #Pharmacetucials #DrugDevelopment #LifeSciences #LondonJobs
INDCP
Were looking for an experienced Medical Writer to join a growing drug development company based in central London focused on advancing innovative oncology treatments.
This is an exciting opportunity to be part of a small agile and collaborative team working across five oncology assets in pre-clinical and early-phase development. Youll work closely with cross-functional experts reporting to the Senior Clinical Scientist to create review and edit high-quality regulatory and scientific documentation that supports the companys development pipeline.
Key Responsibilities:
- Develop and review early-stage clinical study protocols and amendments
- Prepare Investigator Brochures
- Conduct literature reviews to source reference materials and understand the competitive landscape
- Author components of regulatory submissions and responses (e.g. INDs DSURs briefing documents etc.)
- A degree in Life Sciences or a related field; an MSc or PhD is preferred
- Experience in oncology ideally across multiple modalities
- Proven experience as a Medical Writer or Clinical Scientist with the confidence and ability to work independently and proactively across the organisation
- Strong experience writing study protocols amendments and ancillary regulatory documents for Phase I and II oncology trials
#MedicalWriter #ClinicalScience #ScientificWriting #Oncology #CancerResearch #OncologyJobs #EarlyClinicalDevelopment #ClinicalTrials #Biotechnology #Pharmacetucials #DrugDevelopment #LifeSciences #LondonJobs
INDCP
Company Industry
Science & Research
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
