Duration & Type: 12 months Contract with a major pharmaceutical industry client
Location: Summit, New Jersey
Responsibilities:
- This role interacts with senior members of the Medical Writing and Disclosure (MW&D) team, Clinical and Regulatory Operations
- Responsibilities Supporting Medical Writing Activities:
- Perform Quality Checks of clinical and submission documents.
- Format documents and ensure that they meet technical specifications required for publishing.
- Assist the Medical Writer to collate documents and maintain electronic filing.
- Assist the Medical Writer in coordination of reviews.
- Responsibilities supporting Clinical Trial Disclosure Activities:
- Perform Quality Checks of information for protocol registration and results posting.
- Assist in coordination of reviews.
Required:
- Fluent written and spoken English with high levels of competency with respect to grammar and spelling.
- High levels of proficiency with Microsoft Office products, i.e., Word, Excel, PowerPoint.
- Active listening and ability to assimilate information and concepts.
- Keen eye for detail and ability to maintain focus.
- Able to work independently and as part of a team.
- Able to think through a problem and take appropriate action/escalate
- Education: An undergraduate degree with Honors in Pharmacy, Biological Sciences or related disciplines.
For consideration, please send resume to [email protected]
