Palo Alto, CA · On-site
$100 - $125/hr
Stanford University is seeking a Clinical Trial Regulatory lab manager (Clinical Trials Regulatory Specialist 2) to beresponsible for the administration and regulatory compliance of clinical research ...
Palo Alto, CA · On-site
$100 - $125/hr
Stanford University is seeking a Clinical Trial Regulatory lab manager (Clinical Trials Regulatory Specialist 2) to beresponsible for the administration and regulatory compliance of clinical research ...
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Maintain and track essential study documentation, including regulatory documents such as 1572s in ...
Quick apply
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Maintain and track essential study documentation, including regulatory documents such as 1572s in ...
Strong experience in clinical trial regulatory affairs and study start-up activities. * Demonstrated project management experience. * Previous line management and/or matrix management experience.
Strong experience in clinical trial regulatory affairs and study start-up activities. * Demonstrated project management experience. * Previous line management and/or matrix management experience.
Manhattan, NY · On-site
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Review, file, and track clinical trial documentation in accordance with SOPs and regulatory ...
Manhattan, NY · On-site
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Review, file, and track clinical trial documentation in accordance with SOPs and regulatory ...
Bala Cynwyd, PA · On-site
$31.50 - $43/hr
Clinical Trial Associate The Clinical Trial Associate (CTA) supports the Director of Clinical ... Knowledge of and adherence to SOPs and compliance with FDA Code of Federal Regulations.
Bala Cynwyd, PA · On-site
$31.50 - $43/hr
Clinical Trial Associate The Clinical Trial Associate (CTA) supports the Director of Clinical ... Knowledge of and adherence to SOPs and compliance with FDA Code of Federal Regulations.
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Review, file, and track clinical trial documentation in accordance with SOPs and regulatory ...
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Review, file, and track clinical trial documentation in accordance with SOPs and regulatory ...
Hayward, CA · On-site
$38.50 - $52.50/hr
Clinical Trial Associate Location: Onsite, Hayward, CA Department: Clinical Development Employment ... Experience supporting sponsor audits, regulatory inspections, or internal quality audits
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Hayward, CA · On-site
$38.50 - $52.50/hr
Clinical Trial Associate Location: Onsite, Hayward, CA Department: Clinical Development Employment ... Experience supporting sponsor audits, regulatory inspections, or internal quality audits
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Maintain and track essential study documentation, including regulatory documents such as 1572s in ...
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Maintain and track essential study documentation, including regulatory documents such as 1572s in ...
Waltham, MA · On-site
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Maintain and track essential study documentation, including regulatory documents such as 1572s in ...
Waltham, MA · On-site
$90K - $124K/yr
We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the ... Maintain and track essential study documentation, including regulatory documents such as 1572s in ...
Somerset, NJ · Hybrid
$35.50 - $48.25/hr
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Maintain working knowledge of applicable regulations and standards to support ongoing study ...
Somerset, NJ · Hybrid
$35.50 - $48.25/hr
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Maintain working knowledge of applicable regulations and standards to support ongoing study ...
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
$80 - $100/hr
Position Summary The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
$80 - $100/hr
Position Summary The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Somerset, NJ · On-site
$35.50 - $48.25/hr
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Maintain working knowledge of applicable regulations and standards to support ongoing study ...
Somerset, NJ · On-site
$35.50 - $48.25/hr
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Maintain working knowledge of applicable regulations and standards to support ongoing study ...
$35.50 - $48.25/hr
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Maintain working knowledge of applicable regulations and standards to support ongoing study ...
$35.50 - $48.25/hr
Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ... Maintain working knowledge of applicable regulations and standards to support ongoing study ...
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
$86K - $105K/yr
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Newark, CA · On-site
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Quick apply
Newark, CA · On-site
The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory ...
Needham, MA · On-site
$80 - $100/hr
Learn more: www.candeltx.com Position Summary The Clinical Trial Associate (CTA) role supports ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Needham, MA · On-site
$80 - $100/hr
Learn more: www.candeltx.com Position Summary The Clinical Trial Associate (CTA) role supports ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Malvern, AR · On-site
$100 - $125/hr
Position SummaryThe Clinical Trial Manager (CTM) is responsible for the overall operational ... Support regulatory submissions and external safety board data reviews as applicable.Independently ...
Malvern, AR · On-site
$100 - $125/hr
Position SummaryThe Clinical Trial Manager (CTM) is responsible for the overall operational ... Support regulatory submissions and external safety board data reviews as applicable.Independently ...
Clinical Trial Manager/ Sr. Clinical Trial Manager At City Tx, we're building the next generation ... Ensure compliance with GCP, SOPs, and regulatory requirements across all operational activities.
Clinical Trial Manager/ Sr. Clinical Trial Manager At City Tx, we're building the next generation ... Ensure compliance with GCP, SOPs, and regulatory requirements across all operational activities.
$17.31 - $22.12
4% of jobs
$22.12 - $26.92
8% of jobs
$26.92 - $31.73
12% of jobs
$31.88 is the 25th percentile. Wages below this are outliers.
$31.73 - $36.54
26% of jobs
$36.54 - $41.35
18% of jobs
$43.02 is the 75th percentile. Wages above this are outliers.
$41.35 - $46.15
19% of jobs
$46.15 - $50.96
6% of jobs
$50.96 - $55.77
2% of jobs
$55.77 - $60.58
1% of jobs
$60.58 - $65.38
1% of jobs
$65.38 - $70.19
2% of jobs
$17
$39
$70
For Clinical Trial Regulatory Associate jobs, the most frequently searched job titles are:
$100 - $125/hr
Other
Posted 6 days ago
The Stanford Innovative Neurotherapeutics Center, or SINC, is a new center at Stanford University and the Lucile Packard Children's Hospital dedicated to advancing treatments for devastating neuropsychiatric disorders. Stanford University is seeking a Clinical Trial Regulatory lab manager (Clinical Trials Regulatory Specialist 2) to beresponsible for the administration and regulatory compliance of clinical research within SINC, and representing the university with external regulatory agencies, both domestic and international.
DESIRED QUALIFICATIONS:This position is a 1-year fixed term.
