Joulé
Clinical Research Coordinator
Joulé, Encino, California, United States, 91316
Title: Clinical Research Coordinator
Read on to fully understand what this job requires in terms of skills and experience If you are a good match, make an application.Location: Encino, CAType: Full-time, Direct Hire/PermPay Rate: $25-35/hourStart Date: ASAP
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Essential Duties and Responsibilities:
Assisting trial Investigator in screening and review of potential study participants eligibilityMaintaining case report forms, charts and documentationMentoring, training, and high-level oversight of other clinical research coordinators and research assistantsEnsuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirementsCollecting and entering data as necessaryAssist management with potential new hire selection and shadowing processAssist with study start-up, maintenance, and close-out of studies as needed for those on the teamAbility to be flexible with study assignments
Qualifications
Clinical Research Coordinator with 1-2 years of experiencePhlebotomy experience and current certification/license to perform phlebotomy in the state of CaliforniaExcellent verbal & written communication skillsAbility to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-taskingMust be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA GuidelinesExtensive clinical trial knowledge through education and/or experienceSuccessful completion of GCP Certification and Advanced CRC preferredDetail-orientedFamiliarity with the Code of Federal Regulations as they pertain to human subject protectionStrong interpersonal skills
Read on to fully understand what this job requires in terms of skills and experience If you are a good match, make an application.Location: Encino, CAType: Full-time, Direct Hire/PermPay Rate: $25-35/hourStart Date: ASAP
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Essential Duties and Responsibilities:
Assisting trial Investigator in screening and review of potential study participants eligibilityMaintaining case report forms, charts and documentationMentoring, training, and high-level oversight of other clinical research coordinators and research assistantsEnsuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirementsCollecting and entering data as necessaryAssist management with potential new hire selection and shadowing processAssist with study start-up, maintenance, and close-out of studies as needed for those on the teamAbility to be flexible with study assignments
Qualifications
Clinical Research Coordinator with 1-2 years of experiencePhlebotomy experience and current certification/license to perform phlebotomy in the state of CaliforniaExcellent verbal & written communication skillsAbility to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-taskingMust be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA GuidelinesExtensive clinical trial knowledge through education and/or experienceSuccessful completion of GCP Certification and Advanced CRC preferredDetail-orientedFamiliarity with the Code of Federal Regulations as they pertain to human subject protectionStrong interpersonal skills