In-house Clinical Research Associate II
Apply NowLocation:
US
Company:
Worldwide Clinical Trials is a global, midsize CRO focused on innovative clinical research that improves patient care and experiences.
Summary:
This role ensures quality data submission and regulatory document management for clinical trials. Applicants need a Bachelor’s or Nursing Degree and two years of relevant experience.
Requirements:
Hard Skills: Excellent interpersonal, oral, and written communication skills in English, Ability to contribute to a team remotely, Strong customer focus, ability to interact professionally within a sponsor contact, Proficiency in Microsoft Office, CTMS, and EDC Systems
Credentials: Bachelor’s Degree, Nursing Degree
Experience: Minimum of two years experience as an In-House CRA or Clinical Research Coordinator (CRC) required
Job Description:
What you will do
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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
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Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)
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Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
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Perform feasibility studies/site identification activities for potential sites, as requested
What you will bring to the role
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Excellent interpersonal, oral, and written communication skills in English
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Ability to contribute to a team remotely
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Strong customer focus, ability to interact professionally within a sponsor contact
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Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
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Bachelor’s Degree or a Nursing Degree required
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Minimum of two years experience as an In-House CRA or Clinical Research Coordinator (CRC) required
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High level of proficiency in both spoken and written English required
