Clinical Research Associate
Clinical Research Associate
Intellectt Inc
Alameda, CA
See who Intellectt Inc has hired for this role
Role: Clinical Research Associate (CRA) - B
Location: Alameda, CA - 94502
Duration: 06 Months
Description
Must have a minimum of 2 years experience with "clinical research monitoring". Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. Education: Minimum Associate degree (but prefer Bachelor's) and 2 years of Monitoring experience. Challenges: Monitoring position and local to San Francisco Site. Travel - Average 20 to 35 % depends on what is going on and could be anywhere in the United States.
Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. 3-5 Years Experience Level.
Location: Alameda, CA - 94502
Duration: 06 Months
Description
Must have a minimum of 2 years experience with "clinical research monitoring". Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. Education: Minimum Associate degree (but prefer Bachelor's) and 2 years of Monitoring experience. Challenges: Monitoring position and local to San Francisco Site. Travel - Average 20 to 35 % depends on what is going on and could be anywhere in the United States.
Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary. 3-5 Years Experience Level.
-
Seniority level
Associate -
Employment type
Contract -
Job function
Research, Analyst, and Information Technology -
Industries
Staffing and Recruiting
Referrals increase your chances of interviewing at Intellectt Inc by 2x
See who you knowGet notified about new Clinical Research Associate jobs in Alameda, CA.
Sign in to create job alertSimilar jobs
People also viewed
-
CRA- Home-Based (US)
CRA- Home-Based (US)
-
Clinical Research Data Coordinator
Clinical Research Data Coordinator
-
Clinical Research Associate
Clinical Research Associate
-
Clinical Research Study Coordinator, Part-time
Clinical Research Study Coordinator, Part-time
-
Clinical Trial Associate
Clinical Trial Associate
-
Clinical Trial Assistant (CTA)
Clinical Trial Assistant (CTA)
-
Clinical Research Coordinator, Health and Wellbeing
Clinical Research Coordinator, Health and Wellbeing
-
Clinical Research Assistant I
Clinical Research Assistant I
The Henry M. Jackson Foundation for the Advancement of Military Medicine
-
Clinical Trial Assistant - Home Based
Clinical Trial Assistant - Home Based
-
Clinical Research Associate - IVD
Clinical Research Associate - IVD
Looking for a job?
Visit the Career Advice Hub to see tips on interviewing and resume writing.
View Career Advice Hub