Medical Writer / Clinical Scientist

  • Location


  • Sector:

    Life Sciences

  • Salary:


  • Contact:

    Jonathan Richards

  • Contact email:

  • Job ref:


  • Published:

    12 maanden geleden

  • Expiry date:


The Company

- 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.