Role posted on: 29th April 2020
G&L work on a wide variety of regulatory engagements, and we regularly require the skills and expertise of a Clinical expert to join our project teams – both in the UK, EU, and the US. Our clients range from global pharma and biotech corporations, to much smaller boutique companies who rely on G&L to steer them through complex global regulatory requirements.
Our need for clinical consultancy can be anything from a small number of ad-hoc hours of expert advice, to much longer term engagements.
Role Description: Clinical Expert Consultant projects – worldwide
Project activities may involve:
- Module 2.5 and 2.7 authoring (Clinical overviews and summaries)
- Module 5 document compilation and authoring (Clinical Study Reports)
- Clinical development -strategic advice and support
- Act as a certified Expert on Clinical CTD modules
- Clinical literature searches
- Clinical study reports
- Clinical protocols
- Investigator brochure (IB)
- Case Report Forms (CRF)
- Investigational Medicinal Product Dossier (IMPD)
If you would be open to joining our network and getting details of upcoming projects with G&L, please get in touch today.
If you would like to hear more, please send your details to firstname.lastname@example.org today!
G&L Scientific is an equal opportunities employer and welcomes applicants from all sections of the community regardless of their gender, religious belief, political opinion, sexual orientation, disability, age, marital status or race. We recruit based on talent alone and firmly believe that an individual’s background should play no part in the recruitment and selection process. G&L is committed to everyone having the right to work in an environment free from threat of discrimination, intimidation, harassment and abuse. All employees at G&L share the responsibility to challenge discriminatory behaviour and promote equality of opportunity.