Top Research Associate Jobs

Execute and validate bioanalytical and ligand-binding immunoassays, perform PK analysis of clinical samples, maintain electronic lab notebooks, ensure GCLP compliance, support regulatory documentation, and manage general laboratory operations.

Conduct simulation and design of optical imaging systems and piezoelectric ultrasonic transducers using ray tracing and FEM. Build and implement swept-source and spectral-domain OCT systems enhanced by ultrasound, characterize systems in artificial and real tissue, perform benchtop testing and data analysis, design device layouts with CAD, and package ultrasonic transducers while collaborating with an interdisciplinary team to translate devices for medical applications.

Perform mammalian cell culture and viral packaging, extract nucleic acids from cells and brain tissue, prepare NGS libraries, perform PCR and advanced molecular cloning, and follow SOPs and biosafety requirements to enable genome engineering and protein localization studies in mouse brain.

Manage day-to-day lab operations, safety compliance, and inventory/procurement. Support mammalian and microbial culture workflows, equipment maintenance, EHS interactions, shipping/MTA handling, routine lab tasks, and process improvements. Provide occasional on-call emergency response.

Support BREATH Lab research by conducting lab experiments and participant assessments (in-person or virtual). Tasks include neurocognitive testing, supervising MRI/phlebotomy, biospecimen collection and processing, data collection and statistical analysis, equipment maintenance, study coordination, inventory and budget management, assisting manuscript preparation, and supervising undergraduate assistants.

Designs and conducts research experiments under general supervision, analyzes and presents results, conducts literature review, prepares manuscripts and reports, ensures compliance with institutional policies, and supports project logistics and supplies.

Conduct and analyze research experiments in NLP/ML within the Language Technologies Institute, collect and evaluate data, assist with manuscript and grant writing, maintain lab equipment and supplies, and perform other assigned research tasks.

Join the HTS team to build, scale, and run automated high-throughput plate-based assays (384/1536), operate liquid-handling instruments, analyze HTS data, troubleshoot assays, and collaborate across functions to support drug discovery decision-making.

Responsible for independent site monitoring (initiation, monitoring, close-out), ensuring GCP/ICH compliance, managing ISF/TMF filing, IP accountability, safety event verification, site training, recruitment support, CRF/query resolution, and audit readiness. Collaborates with cross-functional teams and sponsors, prepares monitoring reports, and may manage study budgets for stand-alone projects. Frequent travel required to support on-site activities.

Conduct and oversee site monitoring for clinical trials including initiation, interim, and close-out visits (remote and onsite), source data verification, eTMF/CRF review, investigational product accountability, SAE reconciliation, site training and mentoring, regulatory compliance (ICH GCP/FDA/local), study documentation, and collaboration with sponsors and cross-functional teams to ensure protocol adherence and data quality.

Lead CRA provides oversight and mentorship to CRA teams, ensures GCP and protocol compliance, conducts onsite/remote monitoring visits, reviews CRF/source data and regulatory binders, supports hiring/onboarding and billing, assists with CTMS and quality processes, and liaises with cross-functional teams to resolve site issues and support study conduct.

Conduct site monitoring activities for clinical trials including initiation, interim, and close-out visits; ensure protocol/GCP compliance, source/CRF verification, SAE reconciliation, regulatory binder review, investigational product accountability, query resolution, audit prep, and reporting. Collaborate with in-house CRAs, project managers, and sponsors to support site performance and enrollment.

Conduct and oversee clinical trial site monitoring (qualification, initiation, interim, close-out) to ensure protocol, GCP, and regulatory compliance. Perform source data verification/CRF review, eTMF/TMF QC, investigational product accountability, SAE reconciliation, monitoring visit reporting, site training/mentoring, budget oversight for stand-alone studies, and cross-functional coordination with sponsors, data management, and finance.

The Clinical Research Associate is responsible for site management, ensuring protocol compliance, monitoring patient safety, and facilitating communication between the sponsor and investigational sites.

Conduct onsite experimental AMO/quantum-sensing research: operate and troubleshoot cold-atom/laser/optics experiments, design measurements, analyze data and simulations, communicate results, follow safety and screening requirements. PhD required or imminent.

The postdoc will develop novel superconducting detectors for particle physics, involving design, nano-fabrication, device testing, and data analysis.

Conducts supervised research, manages projects, collects and analyzes data, prepares reports, and assists in publications and budgets.

Seeking a Research Associate focused on Drug Metabolism and Pharmacokinetics to conduct bioanalysis, plasma binding studies, and microsomal assays while collaborating with other teams.

The Research Associate will analyze agricultural economic data, assist in research projects, and develop technical skills in data management and statistical analysis.

Oversee site monitoring and management, ensure compliance with protocols, and facilitate recruitment and training for clinical studies.

Responsible for monitoring and managing clinical research sites, ensuring protocol compliance, and supporting subject recruitment and project execution.

As a Clinical Research Associate, you will perform monitoring and site management to ensure compliance with study protocols and regulations while managing ongoing project expectations.

The Clinical Research Associate will monitor clinical sites for adherence to protocols, ensure data integrity, manage communications, and oversee regulatory compliance throughout clinical trials.

The Clinical Research Associate 2 performs site monitoring and management to ensure compliance with study protocols and regulatory guidelines while supporting recruitment and data management activities.

The Clinical Research Associate 2 performs site monitoring, manages projects, and ensures compliance with regulatory requirements while working with clinical trial sites.