What are the responsibilities and job description for the Clinical Research Coordinator position at Matrix Clinical Research?
Benefits:
- 401(k)
- Competitive salary
- Opportunity for advancement
- Paid time off
- Training & development
Job Summary
We are seeking a motivated and detail-oriented Research Coordinator to join our team. The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies.
Responsibilities
· Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
· Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
· Attend all relevant study meetings;
· Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
· Recruit and screen patients for clinical trials and maintain subject screening logs;
· Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
· Design and maintain source documentation based on protocol requirements;
· Schedule and execute study visits and perform study procedures;
· Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;
· Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
· Monitor subject safety and report adverse reactions to appropriate medical personnel;
· Correspond with research subjects and troubleshoot study-related questions or issues;
· Participate in meetings to confirm daily study tasks are assigned to team members and are executed to the expected standards;
· Assist with study data quality checking and query resolution.
· Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
· Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
· Attend all relevant study meetings;
· Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
· Recruit and screen patients for clinical trials and maintain subject screening logs;
· Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
· Design and maintain source documentation based on protocol requirements;
· Schedule and execute study visits and perform study procedures;
· Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;
· Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
· Monitor subject safety and report adverse reactions to appropriate medical personnel;
· Correspond with research subjects and troubleshoot study-related questions or issues;
· Participate in meetings to confirm daily study tasks are assigned to team members and are executed to the expected standards;
· Assist with study data quality checking and query resolution.
Qualifications
- Must have Phlebotomy experience
- Must have 3 years as a coordinator
- Spanish Speaking / Bilingual preferred
Salary : $32 - $42
CRC II -Research Coordinator
Matrix Clinical Research -
Los Angeles, CA
CRC II -Research Coordinator
Matrix Clinical Research -
Huntington, CA
Clinical Research Coordinator
National Institute of Research, Inc. -
Los Angeles, CA
