Medical Writer / Clinical Scientist
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Location
London
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Sector:
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Salary:
Negotiable
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Contact:
Jonathan Richards
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Contact email:
Jonathan.Richards@voltinternational.co.uk
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Job ref:
BBBH1570_1628851271
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Published:
over 2 years ago
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Expiry date:
2021-10-12
- Early phase CRO supporting a varied number of high profile global pharma and biotech clients
- Well respected and experienced leadership team
- Delivering innovative clinical trials across a wide range of therapy areas
The Role
- Compile scientific documentation to include regulatory and clinical research related documentation
- Working in a fast paced environment you will work to high regulatory standards including SOPs, ICH-GCP and other industry guidelines
- Produce clinical Study Protocols, design complex studies taking into account, safety considerations for first-time-in-man studies
- Deliver clinical study report writing, understanding of pharmacokinetic, pharmacodynamic and safety analyses to include modelling and simulation
The Person
- BSc in Clinical Pharmacology or other life Science
- Proven track record of compiling clinical trial documentation to include clinical study protocols, regulatory and ethics submissions
- In depth knowledge of relevant industry standards and guidelines
- Excellent communication skills, both written and verbal required to articulate concepts and ideas to suit the level of understanding of the target audience including patients, physicians or regulators.