About this role
Job Responsibilities: The successful candidate will be a detail-oriented, self-motivated and extremely organized individual with excellent problem-solving skills who understands the importance of teamwork and accuracy. Specific requirements will include: Day-to-day, comprehensive monitoring of global industry, regulatory, financial, clinical and social media sites/feeds using a variety of secondary research resources. Extensive use of many databases including clinical (TrialTrove, Pharmaprojects, Biopharm Insight, etc.), financial and/or commercial sites (Call Street, StreetAccount, Thomson One, etc.) and a full knowledge of their capabilities. News monitoring (global): capture the latest breaking news as closely as possible to when it happens. Social media monitoring (Facebook, LinkedIn, Twitter, etc.) Setting of alerts in many resources as well as on Google and company websites Project team assignments that involve diversified therapy areas and medical device types Collaborating with team members and helping with ad hoc research requests involving in-depth searches for information Reviewing and highlighting of transcripts and slide presentations by leading pharmaceutical and medical device firms focusing on items of interest to specific project needs Client teleconference attendance for kickoff meetings and project update meetings Provide clients with timely, coherent, and accurate research support. Conduct secondary research, assist with database search strategies, and perform fundamental data analysis. Apply knowledge of the regulatory process, pharmaceutical drug development, and clinical trials to provide the highest quality support to clients. Support team during absences Perform other miscellaneous duties as assigned. If you are a qualified candidate, you will hear back directly from our Human Resources contact. We do not send questionnaires or take fees for applying to our job posts.