Clinical Information Specialist

UBC is a global company focused on demonstrating effectiveness, minimizing safety risks, and documenting economic benefits and providing evidence for decision making within the pharmaceutical and device companies. We deliver evidence of value through strategic and scientific services in Health Economics, Health Science Policy, Health Outcomes Research, Systematic Literature Reviews & Meta-Analyses, Pricing & Reimbursement, and Epidemiology & Risk Management. Our evidence-based solutions also include: Data-Resources & Analytics, Life Sciences Training, Investigator Services, Patient Programs, Clinical Trials & Registries, IVR & Web Systems for Clinical Trials, and Electronic Data Capture. Responsibilities: Co-Investigator, or Investigator, for sponsored research projects, responsible for customer contact, defining research questions and writing study protocols, extracting data from medical papers, and providing clinical guidance for projects. Supervising and managing the activities of research team(s) to assure timely collection of clinical studies and data extraction. Interaction with statisticians to assure appropriate and timely statistical analysis. Writing of project reports and manuscripts for publication. Reporting to customers on study results. Professional presentation.

 

 Skills and Experience: Clinical training is an asset.  An MD, PharmD, PhD or RN with experience in the pharmaceutical or biotech industry.  Previous experience with clinical trials and/or systematic reviews and meta-analysis. Experience working with or analyzing clinical data. Ability to adhere to timelines. Professional, organized, detailed-orientated, self-motivated and quality driven. Strong written and verbal communication skills.  Experience in medical writing is a must. Strong general computer skills including standard software such as Microsoft Word, Excel and Access.  Managerial experience is a plus.