Clinical Research Associate at Jobot
Los Angeles, CA 90067
About the Job
Clinical Research Associate | $$$ | Temp to Perm
This Jobot Consulting Job is hosted by: Kaylee Pauley
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $85,000 - $95,000 per year
A bit about us:
We are seeking a dynamic, experienced, and highly motivated individual to join our team as a Consulting Clinical Research Associate. The successful candidate will play a vital role in our mission to revolutionize healthcare by conducting and overseeing clinical trials. The Consulting Clinical Research Associate will be responsible for managing and monitoring clinical studies to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements. This role requires a minimum of 5 years of experience in clinical trials.
Why join us?
Medical, Dental and Vision Insurance
401K
Accrued PTO
HSA
Sick PTO
Holiday Pay
Overtime Hours
Job Details
Job Details:
We are seeking a dynamic, experienced, and highly motivated individual to join our team as a Consulting Clinical Research Associate. The successful candidate will play a vital role in our mission to revolutionize healthcare by conducting and overseeing clinical trials. The Consulting Clinical Research Associate will be responsible for managing and monitoring clinical studies to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements. This role requires a minimum of 5 years of experience in clinical trials.
Responsibilities:
1. Manage and monitor clinical studies, ensuring compliance with protocol, SOPs, GCP, and relevant regulatory requirements.
2. Collaborate with cross-functional teams to develop and implement study protocols, data collection systems, and other research materials.
3. Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
4. Review and verify case report forms and other clinical data for completeness and accuracy.
5. Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to applicable regulatory requirements.
6. Evaluate the quality and integrity of study sites, including site performance and adherence to protocol, and take appropriate action as needed.
7. Develop and deliver training to site staff, including investigators, coordinators, and data management personnel.
8. Prepare and submit written reports, forms, and other materials to the project manager or sponsor.
9. Participate in the development of clinical trial budgets and negotiate contracts with study sites.
10. Assist in the development and implementation of recruitment strategies.
11. Act as a liaison between the company and study site personnel, investigators, and other stakeholders.
Qualifications:
1. Bachelor's degree in a life science, nursing, or related field. Advanced degree preferred.
2. Minimum of 5 years of experience in clinical trials, including experience in site management and monitoring.
3. In-depth knowledge of GCP, ICH guidelines, and other applicable regulatory requirements.
4. Strong understanding of clinical research process, including the development and implementation of protocols, case report forms, and other study-related materials.
5. Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and interact with study site personnel, investigators, and other stakeholders.
6. Strong organizational skills, with the ability to manage multiple projects and priorities in a fast-paced, deadline-driven environment.
7. Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint.
8. Willingness and ability to travel as needed to conduct site visits and attend meetings.
9. Certification as a Clinical Research Associate (CRA) is preferred.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Consulting Job is hosted by: Kaylee Pauley
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $85,000 - $95,000 per year
A bit about us:
We are seeking a dynamic, experienced, and highly motivated individual to join our team as a Consulting Clinical Research Associate. The successful candidate will play a vital role in our mission to revolutionize healthcare by conducting and overseeing clinical trials. The Consulting Clinical Research Associate will be responsible for managing and monitoring clinical studies to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements. This role requires a minimum of 5 years of experience in clinical trials.
Why join us?
Medical, Dental and Vision Insurance
401K
Accrued PTO
HSA
Sick PTO
Holiday Pay
Overtime Hours
Job Details
Job Details:
We are seeking a dynamic, experienced, and highly motivated individual to join our team as a Consulting Clinical Research Associate. The successful candidate will play a vital role in our mission to revolutionize healthcare by conducting and overseeing clinical trials. The Consulting Clinical Research Associate will be responsible for managing and monitoring clinical studies to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements. This role requires a minimum of 5 years of experience in clinical trials.
Responsibilities:
1. Manage and monitor clinical studies, ensuring compliance with protocol, SOPs, GCP, and relevant regulatory requirements.
2. Collaborate with cross-functional teams to develop and implement study protocols, data collection systems, and other research materials.
3. Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
4. Review and verify case report forms and other clinical data for completeness and accuracy.
5. Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to applicable regulatory requirements.
6. Evaluate the quality and integrity of study sites, including site performance and adherence to protocol, and take appropriate action as needed.
7. Develop and deliver training to site staff, including investigators, coordinators, and data management personnel.
8. Prepare and submit written reports, forms, and other materials to the project manager or sponsor.
9. Participate in the development of clinical trial budgets and negotiate contracts with study sites.
10. Assist in the development and implementation of recruitment strategies.
11. Act as a liaison between the company and study site personnel, investigators, and other stakeholders.
Qualifications:
1. Bachelor's degree in a life science, nursing, or related field. Advanced degree preferred.
2. Minimum of 5 years of experience in clinical trials, including experience in site management and monitoring.
3. In-depth knowledge of GCP, ICH guidelines, and other applicable regulatory requirements.
4. Strong understanding of clinical research process, including the development and implementation of protocols, case report forms, and other study-related materials.
5. Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and interact with study site personnel, investigators, and other stakeholders.
6. Strong organizational skills, with the ability to manage multiple projects and priorities in a fast-paced, deadline-driven environment.
7. Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint.
8. Willingness and ability to travel as needed to conduct site visits and attend meetings.
9. Certification as a Clinical Research Associate (CRA) is preferred.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
85,000 - 95,000 /year