Intellectt Inc
Clinical Research Associate (CRA) - B
Intellectt Inc, San Diego, California, United States, 92189
Hello this is Komal from Intellectt we have an opening for a Clinical Research Associate (CRA) - B in San Diego, CA. Please find the job details and description below and if interested You can reach me at komal@intellectt.com or call me at +1(732)-813-9025.
Role : Clinical Research Associate (CRA) - B
Location : San Diego, CA - 92121
Duration : 6 Months
Shift Timings : 9 AM to 5 PM
Responsibilities
Carry out assigned functions applying knowledge and skill in an accurate, timely manner.Apply knowledge of FDA regulations to site monitoring and clinical study design duties.Monitor and maintain necessary supplies, with approval by senior department staff.Maintain effective, professional, timely, and consistent communications with clinical sites both in person, and via all available correspondence media (telephone, email, web, etc.)Support and/or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials)Ability to train site personnel on study activities including investigational product usage, maintenance and accountability, sample collection, testing and shipping, data entry and query resolution.Study monitoring (includes assessing the familiarity of the site personnel with the protocol, procedures and investigational product, assessing protocol compliance and investigational product accountability as applicable, source document verification, identifying protocol deviations, writing queries, writing monitoring reports, notes to file, and other documentation as necessary)Independent site management skills to assist with study problem identification and solving, and ensure timely study progression.Understanding of clinical research activities including tasks associated with study start up, interim monitoring, close out, data collection and central files.Team player able to deliver on project timelines.Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships.Other duties as assigned, according to the changing needs of the business.Top 3 Skills
Experience 2-5 years.Experience with study start up, monitoring, and close out activities.Ability to work independently, get training done and be able to hit the ground quickly.
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Role : Clinical Research Associate (CRA) - B
Location : San Diego, CA - 92121
Duration : 6 Months
Shift Timings : 9 AM to 5 PM
Responsibilities
Carry out assigned functions applying knowledge and skill in an accurate, timely manner.Apply knowledge of FDA regulations to site monitoring and clinical study design duties.Monitor and maintain necessary supplies, with approval by senior department staff.Maintain effective, professional, timely, and consistent communications with clinical sites both in person, and via all available correspondence media (telephone, email, web, etc.)Support and/or lead clinical research study start up activities (includes creation of study binders, study logs, work instructions, case report form, and other study related materials)Ability to train site personnel on study activities including investigational product usage, maintenance and accountability, sample collection, testing and shipping, data entry and query resolution.Study monitoring (includes assessing the familiarity of the site personnel with the protocol, procedures and investigational product, assessing protocol compliance and investigational product accountability as applicable, source document verification, identifying protocol deviations, writing queries, writing monitoring reports, notes to file, and other documentation as necessary)Independent site management skills to assist with study problem identification and solving, and ensure timely study progression.Understanding of clinical research activities including tasks associated with study start up, interim monitoring, close out, data collection and central files.Team player able to deliver on project timelines.Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships.Other duties as assigned, according to the changing needs of the business.Top 3 Skills
Experience 2-5 years.Experience with study start up, monitoring, and close out activities.Ability to work independently, get training done and be able to hit the ground quickly.
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