Top Research Associate Jobs

Provide support for clinical trials, including protocol design, site evaluations, study monitoring, and report preparation under supervision.

The Clinical Research Associate II assists in the design, preparation, and monitoring of clinical trials, ensuring protocol adherence and managing study documentation.

Assist in clinical research support, including protocol preparation, site evaluation, study monitoring, documentation, and report generation for clinical trials.

This role involves supporting clinical trials through protocol preparation, monitoring site compliance, managing budgets and regulatory documents, and conducting site visits.

Assist in the design and monitoring of clinical trials, prepare protocols and necessary materials, conduct site visits, and ensure compliance with regulations.

Provide support for clinical trials by assisting in protocol design, conducting site evaluations, managing documents, and performing study monitoring.

Assist in the design and preparation of clinical protocols, conduct site evaluations, manage projects, monitor studies, and maintain documentation.

Provide support for clinical trials by assisting in protocol design, monitoring studies, evaluating clinical sites, and preparing reports.

The Clinical Research Associate supports clinical trials by assisting in protocol design, budget procurement, study monitoring, and preparing reports.

The Sr. Clinical Research Associate provides support for clinical trials, including protocol preparation, site evaluations, study monitoring, and report generation.

This role supports clinical trials by assisting in protocol design, site evaluation, monitoring studies, and ensuring adherence to guidelines and regulations.

The Clinical Research Associate 1 provides support for clinical trials, assists in protocol design, site evaluations, monitoring, and regulatory document preparation.

The Senior Clinical Research Associate manages site monitoring and relationships for clinical trials, ensuring compliance and patient safety according to GCP and regulations.

The Clinical Research Associate manages relationships with site personnel to ensure clinical trials comply with regulatory standards and protect participant wellbeing, while overseeing site monitoring and data accuracy.

The Senior Research Associate will develop and optimize an AAV platform, support preclinical supply, and manage lab operations, with strong experience in cell culture and viral vector production.

Join NewLimit as a Senior/Research Associate to perform large-scale single cell perturbation experiments, molecular cloning, and viral vector applications. Contribute to improving epigenetic therapies.

The Senior Clinical Research Associate will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.

Contract Research Associate supporting Analytical Development to develop, optimize, qualify, and validate analytical methods for cell therapy products; perform hands-on laboratory studies, generate and document data, author SOPs/protocols, collaborate cross-functionally, and maintain equipment and compliance.

Postdoctoral researcher will develop and validate remote-sensing-enabled surface and groundwater models, integrate NASA EO products with in situ data, apply hydrologic and groundwater models, build AI/ML predictive frameworks, manage heterogeneous datasets, support tool development (APIs/dashboards), engage binational stakeholders, publish research, and supervise students.

Perform and design immunology research using murine lung disease models, advanced flow cytometry and cell sorting, molecular assays (qPCR, bulk and single-cell RNAseq, TCRseq), spatial transcriptomics, microscopy, and cell culture. Maintain animal colonies, biosafety/IACUC compliance, lab inventory, records, and QC. Analyze data with FlowJo, Prism, and R; prepare manuscripts, figures, and grant materials; and train/supervise junior staff and coordinate core collaborations.

Execute and design experiments to support reagent and assay development, analyze data, prepare reports/presentations, maintain lab inventory and supplies, perform BSL-2 laboratory work, troubleshoot experiments, and collaborate on research initiatives with limited supervision.

Conduct laboratory experiments, prepare and analyze specimens and tissue cultures, perform routine assays and statistical analyses, maintain and operate lab equipment, follow research protocols and good research practices, and contribute to publications and ongoing learning.

The Clinical Research Coordinator 1 assists in managing clinical research protocols, conducts participant eligibility checks, coordinates study activities, and ensures compliance with regulatory standards.

The role involves conducting in vitro assays, analyzing samples, maintaining cell lines, and collaborating with a team on experimental design.

Manage site selection, initiation, monitoring (onsite and remote), and closure for assigned clinical study sites. Ensure compliance with ICH-GCP and sponsor/client standards, maintain study documentation (eTMF/ISF), drive site performance, manage drug accountability, report SAEs, update CTMS, and support audits/inspections and local study team activities.