In-House Clinical Research Associate
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Job Description
Clinical Research Associate ensuring data quality and regulatory compliance for clinical trials. Engaging with diverse teams to facilitate efficient execution of studies and support patient care.
Responsibilities:
- Ensure quality of data submitted from study sites and assure timely submission of data
- 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
Requirements:
- Excellent interpersonal, oral, and written communication skills
- 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
- 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 or other experience deemed relevant
- Proficiency in English and at least one of the following languages: German, Polish or Italian.
Benefits:
- Health insurance
- Remote work options
- Paid time off
- Professional development opportunities
- Inclusive workplace culture
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