CRI Lifetree Salt Lake City, Utah is currently recruiting the following positions. Qualified applicants for these positions are invited to submit their resumes to email@example.com
APRN - Qualifications: The successful candidate must have a minimum of 2 years of experience with documentation of previous certifications for neuroscience rating scales such as: PANS, MADRS, HAM-D, CGI, CGIS, Mini, MMSE, CCER and EDS. Responsibilities: The successful candidate will have direct contact with research subjects for the purposes of administering and scoring selected battery of neuropsychology testing in accordance with clearly defined research protocols, interactions with clinical research sponsors and our onsite clinical research coordinating team. Prior research experience is preferred with a working knowledge of HIPAA, GCP, ICH, E6, and FDA Regulations.
Clinical Research Coordinator to join our neuroscience research team. Qualifications: RN, LPN, MA with minimum of one year experience with mild cognitive impairment/Alzheimer’s clinical trials is preferred. Responsibilities: This position is responsible for conducting clinical protocol visits, interacting with sponsors and working within a project team environment. Working knowledge of ICH, GCP, E6, FDA Regulations, OSHA and HIPAA are preferred.
Part-time pharmacy technician to work in a clinical research setting. The pharmacy technician will work under the direct supervision of our registered pharmacist. Qualifications: The successful candidate will have completed a pharmacy technician training program and current licensure by the Utah Board of Pharmacy. Must be able to maintain a flexible work schedule including some weekends and have strong attention to detail. Experience working in a research setting is preferred. Responsibilities: The pharmacy technician will assist the research pharmacist in all aspects of pharmacy activities that support CRI Lifetree clinical research operations.
Part-time Quality Assurance Associate (QAA) to join our internal quality assurance (QA) team. Qualifications: The successful candidate will have minimum of 2 years’ experience in a QA role within the biopharma industry. Must have a working knowledge of HIPAA, GCP, ICH, E6, and FDA Regulations. Responsibilities Include: Implementation and maintenance of CRI Lifetree’s internal quality assurance systems, Real Time Quality Assurance during the execution phase of clinical trials and internal compliance audits with CRI Lifetree SOPs and Work Instructions. Responsible for developing and executing Quality Plans for CRI Lifetree studies.