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YesterdaySaved
Remote
United States of America
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead clinical data review for studies, ensuring the interpretation of efficacy and safety data, and collaborating with cross-functional teams.
Top Skills: Clinical Trial Data Analysis ToolsGCPIch GuidelinesMeddraWho Drug
Reposted YesterdaySaved
Remote
Texas, USA
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Senior Clinical Research Associate, you will act as the primary liaison between investigational sites and the sponsor, conducting site visits, ensuring compliance, monitoring patient safety, and assisting in recruitment efforts.
Top Skills: CtmsEtmfIch-Gcp
Reposted YesterdaySaved
Remote
United States of America
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Principal Clinical Data Science Lead will oversee data science methodologies in clinical research, manage teams, and ensure data insights support clinical development.
Top Skills: ElluminateJreviewMedidataRshinyVeeva
Reposted YesterdaySaved
Remote
United States of America
Mid level
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.
Top Skills: Clinical Trial ProcessesIch-Gcp Guidelines
Reposted 2 Days AgoSaved
Remote
United States of America
Junior
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.
Top Skills: Clinical Trial ProcessesIch-Gcp Guidelines
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Reposted 2 Days AgoSaved
Remote
United States of America
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.
Top Skills: Clinical Trial SoftwareGood Clinical Practice (Gcp)Life SciencesMedicineNursing
Reposted 3 Days AgoSaved
Remote
United States of America
Entry level
Entry level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.
Reposted 3 Days AgoSaved
In-Office or Remote
3 Locations
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.
Top Skills: Clinical Trial ManagementFda RegulationsGCPIch
Reposted 3 Days AgoSaved
Remote
United States of America
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Responsible for monitoring cardiovascular medical device studies, ensuring compliance with FDA regulations, and fostering effective relationships with stakeholders.
Top Skills: Clinical Trial ManagementFda RegulationsIch/Gcp Guidelines
Reposted 3 Days AgoSaved
In-Office or Remote
Texas, USA
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
Senior Site Monitor responsible for planning and conducting on-site and remote monitoring across Phase I-IV studies. Ensures site compliance with protocol, data quality, and participant safety, conducts source data verification, manages site communications, supports RBQM processes, and participates in audits and inspections.
Top Skills: CtmsEcoaRbqmTmfVeeva Edc
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