Affygility Solutions is recruiting for a toxicology process manager in the area of manuscript generation to join our team of scientists supporting the pharmaceutical industry. This is a non-laboratory position that is central to the efficient, high quality delivery of our OEL Fastrac(TM) documents to clients. This is a 100% remote position, and the successful applicant can work from their desired location in the United States or Canada (Quebec only) as part of a high-performing, highly integrated, globally distributed team.
Affygility Solutions works with companies in nearly 70 countries and continues to experience significant year-on-year growth.
In this position, you will coordinate the activities of information science, manuscript generation by toxicology staff, and document quality control activities consistent with the deadlines required by our customers. You will be responsible for understanding and working with the throughput capabilities of the related functions. You will coordinate and assign activities in a manner that is consistent with capabilities and the agreed deadlines and will be responsible for identifying throughput challenges.
With your background in either toxicology or a related field (e.g. biology, pharmacology, chemistry with considerable biology training, etc.) and familiarity with toxicology concepts, you also will assist, as needed, with the generation of manuscripts (such as PDE reports) by performing literature-based research and organizing relevant information in support of manuscript preparation.
Excellent analytical abilities, attention to detail, writing skills, time management, organizational skills, and the ability to work to established timelines are a must. Previous experience in the pharmaceutical, agrochemical or chemical industries is a plus. Experience with process management is highly desirable.
Some travel to team meetings or conferences may be required, but expected to be a minor requirement.
Affygility Solutions offers a competitive compensation and benefits package.