Regulatory Scientific Communications Associate

Scientific Communications Associate - Regulatory needed for major pharmaceutical client in Indianapolis, IN!

 

Scientific Communication Associate tasks could include developing, coordinating, and writing Phase 1-3 study protocols and FDA-ready study reports and synopses as well as all scientific and medical publication writing for the promotion of a novel therapeutic-based therapy (oncology).  Consultant will interface with other team components, such as physicians, data management personnel, and statisticians, as well as, coordinating site investigators to develop abstracts / presentations / manuscripts. Consultant will critically interpret and analyze scientific and clinical data and biostatistics.

 

Necessary Skills: Demonstrated writing experience or aptitude. A writing test is required as a part of the candidate evaluation process.  Excellent analytical, interpersonal, project management, and leadership skills.  Excellent written and oral communication skills.  Ability to develop high-level end-user computer skills (i.e., word processing, tables and graphics, spreadsheets, presentations, and templates).  Ability to work independently and as part of a team.  Demonstrated technical editing skills.  Demonstrated command of English grammar, knowledge of correct word usage and sentence structure.  Excellent attention to detail. General knowledge of scientific literature and online literature searches (Medline) is helpful. Ability to work with minimal supervision and maintain a high level of productivity.  Ability to juggle multiple conflicting deadlines.

 

Education, Experience, Training:  Bachelors degree required, preferably in science;  Graduate degree preferred. Scientific, medical, or pharmaceutical training/experience preferred.  Prior publication history (4+ years) preferred.  Demonstrated knowledge of global clinical data validation process is preferred.