Clinical Trial Assistant / Senior Clinical Trial Assistant at Jobot
Mountain View, CA 94043
About the Job
Pharma Company that focuses on Oncology
This Jobot Job is hosted by: Victoria Casal
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $70,000 - $110,000 per year
A bit about us:
Our client has been in business since 2011, focusing on developing innovative medicines for major diseases like cancer. With a strong pipeline of 23 assets, 4 approved products in China.
Why join us?
Competitive base
Benefits
PTO
401K with match
bonus potential
Flexible work environment
Job Details
MUST SPEAK ENGLISH AND CHINESE
Responsibilities
1. Assist in the coordination and management of clinical trials from startup to closeout.
2. Maintain and update the Clinical Trial Management System (CTMS) and Electronic Data Capture (EDC) system.
3. Prepare and review study documents including Case Report Forms (CRF), informed consent forms, and study manuals.
4. Monitor the progress of clinical trials and ensure they are conducted, recorded, and reported in accordance with protocol, SOPs, GCP, and regulatory requirements.
5. Assist in the preparation of site visit reports and follow-up letters.
6. Coordinate with clinical sites and internal teams to ensure timely and accurate data collection and entry.
7. Participate in team meetings, providing updates on trial progress and issues.
8. Assist in the development and implementation of patient recruitment strategies.
9. Ensure all trial supplies are accounted for and manage the inventory of trial materials.
10. Coordinate the shipment and receipt of study materials and investigational products to and from clinical sites.
Qualifications
1. Bachelor’s degree in life sciences or related field.
2. Minimum of 2 years of experience in clinical research or related field.
3. Experience with CRF, Study Monitoring, GCP, CTMS, EDC, TMS, and Clinical Trial Management.
4. Strong understanding of clinical trial processes and regulatory requirements.
5. Excellent organizational skills with the ability to prioritize and manage multiple tasks.
6. Strong written and verbal communication skills.
7. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
8. Ability to work independently and as part of a team.
9. Strong attention to detail and problem-solving skills.
10. Availability to travel as needed to support clinical trial activities.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Victoria Casal
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $70,000 - $110,000 per year
A bit about us:
Our client has been in business since 2011, focusing on developing innovative medicines for major diseases like cancer. With a strong pipeline of 23 assets, 4 approved products in China.
Why join us?
Competitive base
Benefits
PTO
401K with match
bonus potential
Flexible work environment
Job Details
MUST SPEAK ENGLISH AND CHINESE
Responsibilities
1. Assist in the coordination and management of clinical trials from startup to closeout.
2. Maintain and update the Clinical Trial Management System (CTMS) and Electronic Data Capture (EDC) system.
3. Prepare and review study documents including Case Report Forms (CRF), informed consent forms, and study manuals.
4. Monitor the progress of clinical trials and ensure they are conducted, recorded, and reported in accordance with protocol, SOPs, GCP, and regulatory requirements.
5. Assist in the preparation of site visit reports and follow-up letters.
6. Coordinate with clinical sites and internal teams to ensure timely and accurate data collection and entry.
7. Participate in team meetings, providing updates on trial progress and issues.
8. Assist in the development and implementation of patient recruitment strategies.
9. Ensure all trial supplies are accounted for and manage the inventory of trial materials.
10. Coordinate the shipment and receipt of study materials and investigational products to and from clinical sites.
Qualifications
1. Bachelor’s degree in life sciences or related field.
2. Minimum of 2 years of experience in clinical research or related field.
3. Experience with CRF, Study Monitoring, GCP, CTMS, EDC, TMS, and Clinical Trial Management.
4. Strong understanding of clinical trial processes and regulatory requirements.
5. Excellent organizational skills with the ability to prioritize and manage multiple tasks.
6. Strong written and verbal communication skills.
7. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
8. Ability to work independently and as part of a team.
9. Strong attention to detail and problem-solving skills.
10. Availability to travel as needed to support clinical trial activities.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
70,000 - 110,000 /year