Hamlyn Williams have partnered with a growing biotech in Boston who are looking to rapidly grow their team within the next 24 months. The growth plans start with a Junior/Senior Medical Writer who will join them and help build out their regulatory writing team.

They are happy to look at candidates crossing over from other funcitons of Medical Writing such as communications or candidates with scientific/labatory exeperience. However experience working within the regulatory (Life Sciences) space would be beneficial.

Responsibilities/Duties

•Author complex clinical documents (e.g. protocols, phase II/III clinical study reports, high level summary documents) as well as non-clinical documents (e.g. initial Investigator’s Brochure).

•Reviews and edits documents as required.

•Manage external CRO's and Consultancys as neccessary

•Participate in appropriate strategy meetings

•Timely completion and high quality of assigned documents

Qualifications/Requirements

•Advanced proficiency in Microsoft Office Suite (e.g., Word, Excel, PowerPoint, and Outlook).

•Master’s (Scientific), PhD, or PharmD

•Ability to produce detailed, comprehensive documentation

This is a great opportunity to work within a field (Regulatory Writing) that has a large candidate shortage which will help advance your career within the Medical Writing space

For more information please contact samuel banks either on +347 242 5722 or send your Cv to s.banks@hamlynwilliams.com

Job

Medical Writer- Boston- Permanent