The Senior Research Associate, in collaboration with the Principal Investigators, will be responsible for the planning, implementation, and execution of clinical trials in the assigned department. Primary responsibilities include the coordination of study enrollment; oversight of study protocols; and submission of research activities per IRB regulations. The incumbent will establish and maintain databases of subjects; monitor data collection for accuracy; process informed consent paperwork; and ensure that study payment is processed and received in a timely fashion. Additional responsibilities include working independently to drive day-to-day research activities; monitoring and tracking expenditures; supporting multiple active protocols simultaneously; and working with multiple investigators while adhering with FDA, IRB, Pennsylvania, and related regulations. Performs other duties as assigned. Required Education and Experience: Bachelor's degree in life science, health professions or related field and four years of directly related clinical research coordinator experience. An equivalent combination of education and experience may be considered. Required Skills and Abilities:
...Brandeis seeks to hire a temporary Grant Accountant in Central Finance. This position is 35 hours a week for approximately 3 months. Please submit a cover letter and resume. Key Responsibilities: Performs post audit of grant expense activity to...
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...Immediate need for a Physician Assistant or Nurse Practitioner to join a Orthopedic group in an Urgent Care Setting. Lets discuss We are looking for someone for Urgent Care, they need to be experienced and they need to be willing to work a few night shifts. I am rotating...