Clinical Research Associate III
Clinical Research Associate III – Jinsong
Location: Remote (Pacific Time Zone Preferred)
Schedule: Monday–Friday, 8:00 AM–5:00 PM PST
Contract Duration: 6 month contract with opportunity to extend
Pay Rate: $35–$45/hour or about $90,000 a year
Position Overview
As a Clinical Research Associate (CRA III) at this company you will play a critical role in ensuring the successful execution of clinical trials from study initiation through closeout. This position collaborates closely with investigators, study coordinators, and cross-functional internal teams including Research & Development, Finance, Marketing, and other core stakeholders.
The ideal candidate will have experience monitoring clinical studies, maintaining regulatory compliance, and supporting high-quality data collection and documentation in accordance with GCP and regulatory guidelines.
Key Responsibilities
• Conduct Site Initiation Visits (SIVs), routine monitoring visits, and closeout visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP)
• Perform source data verification (SDV), data collection, and query resolution to ensure data accuracy and integrity
• Maintain and organize study documentation, including regulatory files and Trial Master Files (TMF)
• Collaborate with cross-functional teams to support timely and efficient study execution
• Prepare and submit monitoring reports, follow-up letters, and other study-related documentation
• Track site performance, identify issues proactively, and escalate concerns as needed
• Support overall study management activities and ensure adherence to timelines and quality standards
Qualifications
• Bachelor’s degree required
• Minimum of 1–2 years of experience as a Clinical Research Associate (CRA) or in a similar clinical research role
• Strong understanding of clinical trial processes, FDA regulations, ICH-GCP guidelines, and industry standards
• Excellent communication, organizational, and time management skills
• Ability to work independently in a remote environment while managing multiple priorities
• CRA certification is a plus
Additional Information
• Fully remote position
• Candidates located in or able to support Pacific Time Zone working hours preferred
• Opportunity to work with a collaborative and innovative clinical research team
Apply tot his job
Apply To this Job
Location: Remote (Pacific Time Zone Preferred)
Schedule: Monday–Friday, 8:00 AM–5:00 PM PST
Contract Duration: 6 month contract with opportunity to extend
Pay Rate: $35–$45/hour or about $90,000 a year
Position Overview
As a Clinical Research Associate (CRA III) at this company you will play a critical role in ensuring the successful execution of clinical trials from study initiation through closeout. This position collaborates closely with investigators, study coordinators, and cross-functional internal teams including Research & Development, Finance, Marketing, and other core stakeholders.
The ideal candidate will have experience monitoring clinical studies, maintaining regulatory compliance, and supporting high-quality data collection and documentation in accordance with GCP and regulatory guidelines.
Key Responsibilities
• Conduct Site Initiation Visits (SIVs), routine monitoring visits, and closeout visits to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP)
• Perform source data verification (SDV), data collection, and query resolution to ensure data accuracy and integrity
• Maintain and organize study documentation, including regulatory files and Trial Master Files (TMF)
• Collaborate with cross-functional teams to support timely and efficient study execution
• Prepare and submit monitoring reports, follow-up letters, and other study-related documentation
• Track site performance, identify issues proactively, and escalate concerns as needed
• Support overall study management activities and ensure adherence to timelines and quality standards
Qualifications
• Bachelor’s degree required
• Minimum of 1–2 years of experience as a Clinical Research Associate (CRA) or in a similar clinical research role
• Strong understanding of clinical trial processes, FDA regulations, ICH-GCP guidelines, and industry standards
• Excellent communication, organizational, and time management skills
• Ability to work independently in a remote environment while managing multiple priorities
• CRA certification is a plus
Additional Information
• Fully remote position
• Candidates located in or able to support Pacific Time Zone working hours preferred
• Opportunity to work with a collaborative and innovative clinical research team
Apply tot his job
Apply To this Job