Description
A global CRO are looking for a Senior Medical Writer on an initial 6 month contract to join the regulatory affairs outsourcing group.An exciting and stimulating project, with numerous challenges will require a regulatory writer with 3-5 years of experience and one with exposure to working with pharma/industry specialists and clients
Candidate requirements:
*3 to 5 years of experience of medical or technical writing either in CRO or pharmaceutical industry.
*Good experience of global clinical trials.
*Significant transferable clinical research or academic research experience.
*Excellent knowledge of ICH-GCP Guidelines and global regulatory guidance.
*Superior knowledge of clinical trials methodology.
*Sound knowledge of EU Disclosure work, clinical study reports, investigator brochures and patient safety narratives
*Experience of writing manuscripts/medical information writing
They want someone who has written CSRs, IBs and protocols independently. Manuscript experience is nice but not mandatory.
If you are interested in applying for this role please send an up to date CV, your location and availability to start. They are looking for someone to start immediately.
Remember to pass onto friends and family members as we offer referral vouchers for successfully placed referrals.
Thanks and best regards,