In-House Clinical Research Associate (In-House CRA) - Home-based - Japanese-speaking
Published 2023-04-14
What you will do
Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.) Provide applicable updates for site related documentation for filing in the Trial Master File (TMF) Perform feasibility studies/site identification activities for potential sites, as requested What you will bring to the role
Excellent interpersonal, oral, and written communication skills in English and local language Ability to contribute to a team remotely Strong customer focus, ability to interact professionally with a sponsor contact Proficiency in Microsoft Office, CTMS, and EDC Systems Your background
Four-year college curriculum with a major concentration in life science preferred but not required, OR Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant
