Top Research Associate Jobs

The Research Associate will design and execute experiments in RNA therapeutics, manage RNA/cell cultures, and analyze data while maintaining documentation.

Coordinate and monitor clinical trials, maintain study documentation and status reports, manage queries and study cost efficiency, ensure regulatory compliance and patient safety, and build relationships with investigators and site staff.

As a Clinical Research Associate II, you'll conduct clinical trial visits, ensure protocol compliance and data integrity, and collaborate with site staff.

The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

As a Clinical Research Associate, you will liaise with investigational sites, ensuring compliance, monitoring studies, maintaining documentation, and supporting recruitment efforts in oncology trials.

As a Clinical Research Associate, you will manage site visits, ensure compliance with regulations, and oversee patient safety and data quality in oncology trials.

The Senior Clinical Research Associate monitors clinical trials, ensures compliance with guidelines, supports studies, mentors junior staff, and maintains audit readiness.

The Clinical Research Associate will manage site interactions, ensure compliance, monitor trials, track data, and facilitate training and recruitment for oncology studies.

The Clinical Research Associate manages site contact for oncology studies, ensures compliance and safety, conducts monitoring, and supports recruitment and training efforts.

The Clinical Research Associate coordinates site activation, monitors compliance with clinical trials, and ensures all necessary documents are completed in accordance with regulatory standards.

Manage oncology site selection and start-up activities including SQVs, regulatory document collection, contract management, KPI monitoring, stakeholder communication, and site activation to Green Light status while ensuring GCP/ICH compliance.

The Clinical Research Associate conducts site visits, ensures compliance with regulations, monitors patient safety, and aids in subject recruitment and data management.

Monitor and manage clinical study sites, ensuring regulatory compliance and adherence to study protocols. Facilitate communication and resolve issues to support site performance.

Support senior equity analysts by researching biotech companies, analyzing clinical and financial data, building financial models, developing investment theses, producing reports, and recommending buy/hold/sell actions while monitoring portfolio positions.

The role involves coordinating start-up processes for clinical trials, ensuring compliance, and maintaining documentation while collaborating with site personnel and operations teams.

As a Clinical Research Associate II, you will monitor late phase studies, ensure protocol compliance, collaborate with site staff, and conduct trial visits.

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

Conduct site selection, initiation, monitoring, and close-out visits for oncology clinical trials; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor safety reporting, drug accountability, recruitment, data quality, and escalate issues while collaborating with cross-functional clinical teams.

Perform site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety. Collaborate with site staff, review data and resolve queries, and contribute to study documentation and clinical study reports.

The Clinical Research Associate will manage site interactions, ensure compliance with regulations, monitor patient safety, and track budgets while supporting recruitment efforts and data quality.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

Looking for a Scientist I, Research Associate to provide laboratory support in developing and commercializing CMP products by conducting experiments and analyzing data.

Conduct site visits for clinical trials, ensure protocol compliance, review data integrity, and collaborate with site staff and investigators.