Description
I have a NEW LIVE Contract Position for an experienced REGULATORY Medical Writer to sit in my clients ONCOLOGY team. The role is based in Woodcliffe Lake in New Jersey (3 days on site) and has a great duration of 12 months, extendable up to 3 years.Key Skills:
-Previous experience (5 years) working as a Regulatory Medical Writer at a MAJOR PHARMA
-Prior Oncology experience is desirable but not essential
-Previous Experience Preparing Regulatory Documents in accordance with ICH guidelines, international regs, standards and processes and the companies Writing Style guides.
Documents include for example:
-Protocols and Protocol amendments
-Clinical Study Reports
-Investigatory Brochures
-Submission Docs
Qualifications:
Bachelors Degree in Life Sciences
Masters/ PHD, Life Sciences, Pharma D
Ideally my client is wanting the contractor on site for 3 DAYS A WEEK** Please note, I am not looking for someone with just Medical Education, Journal and Academia Experience ONLY**
If you are interested, please detail your availability, desired hourly rate and attach an updated resume (). If you are not available right now, please feel free to attach your latest resume and detail your next availability.
To find out more about Real please visit www.realstaffing.com