Intellectt Inc
Clinical Research Associate (Only on w2)
Intellectt Inc, Alameda, California, United States, 94501
Role:
Clinical Research Associate (CRA) - BLocation:
Alameda, CA - 94502Duration:
12 Months on W2Shift Timings:
8 am to 5 pmQualifications:Bachelor's degree required, with a preference in Biological Sciences; Life Sciences degrees will also be considered.Minimum of 3 to 5 years of clinical experience within the industry.Specifically looking for monitoring experience on the sponsor side.Critical to have direct site monitoring experience, as this candidate will be the contact for these sites.Experience with site selection and monitoring visits.Medical device experience of at least 1 year is required; IVD experience is strongly preferred.Pharmaceutical background may also be considered.Experience coordinating site initialization and site closure.Familiarity with IRB (Institutional Review Board) submission and ICF (informed consent forms) revision.Experience editing/revising CRF (case report forms).Familiarity with data cleaning and database processes (queries).Basic MS Office skills, including Outlook, Project, PowerPoint, and Excel.Experience training PI staff.Familiarity with HCI guidelines.Viva experience for electronic filing is preferred.Take ownership and coordinate shipping out devices, the return of devices, and device accountability.Additional Information:Manager will consider candidates who are willing to relocate at their own expense.If the candidate makes it to the second phase of interviews, it will be via video panel for local candidates.Position is 1 year from the start date with possible extensions.Position is onsite only.Contact:Thanks & Regards,Anjali BTechnical RecruiterIntellectt.IncExt: 265Direct: 7327693774517 Route 1 South, Suite 1115 Iselin, NJ 08830In case of my absence, please reach out to my team lead at Anusha@intellectt.com.
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Clinical Research Associate (CRA) - BLocation:
Alameda, CA - 94502Duration:
12 Months on W2Shift Timings:
8 am to 5 pmQualifications:Bachelor's degree required, with a preference in Biological Sciences; Life Sciences degrees will also be considered.Minimum of 3 to 5 years of clinical experience within the industry.Specifically looking for monitoring experience on the sponsor side.Critical to have direct site monitoring experience, as this candidate will be the contact for these sites.Experience with site selection and monitoring visits.Medical device experience of at least 1 year is required; IVD experience is strongly preferred.Pharmaceutical background may also be considered.Experience coordinating site initialization and site closure.Familiarity with IRB (Institutional Review Board) submission and ICF (informed consent forms) revision.Experience editing/revising CRF (case report forms).Familiarity with data cleaning and database processes (queries).Basic MS Office skills, including Outlook, Project, PowerPoint, and Excel.Experience training PI staff.Familiarity with HCI guidelines.Viva experience for electronic filing is preferred.Take ownership and coordinate shipping out devices, the return of devices, and device accountability.Additional Information:Manager will consider candidates who are willing to relocate at their own expense.If the candidate makes it to the second phase of interviews, it will be via video panel for local candidates.Position is 1 year from the start date with possible extensions.Position is onsite only.Contact:Thanks & Regards,Anjali BTechnical RecruiterIntellectt.IncExt: 265Direct: 7327693774517 Route 1 South, Suite 1115 Iselin, NJ 08830In case of my absence, please reach out to my team lead at Anusha@intellectt.com.
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