Top Research Associate Jobs

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

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.

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

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

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 monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

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.

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.

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.

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.

As a Research Associate, you will conduct equity research, develop financial models, analyze investments, and produce actionable market insights, while advancing through a structured professional development track.

Support retained search engagements by leading research and recruiting strategy, mapping targets, managing CRM, coordinating with teams, and driving candidate sourcing and reporting throughout search lifecycles.

Hands-on scientist to perform and document routine iPSC culture, directed differentiations, cell banking and QC (mycoplasma/sterility), DNA extraction for WGS, reagent preparation, and help develop SOPs to stabilize lab processes.

Assist in the Laboratory Sciences department with daily operations, maintain equipment, prepare materials for assays, and document laboratory records.

Support clinical trial operations through protocol interpretation, document collection and TMF maintenance, site start-up and training, supplier coordination, IP and specimen tracking, invoice reconciliation, and cross-functional collaboration to ensure compliant, efficient study conduct.

The Research Associate develops and executes high-throughput assays, manages data, and collaborates in a dynamic environment focusing on generative AI applications in biology.

The Research Associate II will perform protein purification experiments, conduct quality control, maintain lab documentation, and ensure lab safety and cleanliness.

Conduct laboratory work including synthesizing and testing samples, maintaining equipment, and documenting results. Requires good communication skills and attention to detail.

The Research Associate will assist the Private Capital Practice by conducting secondary research, providing data analysis, and supporting consultants with insights and client projects.