Clinical Research Associate: Average Salary in Torrance, CA in 2024

Clinical Research Associate II will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor's degree in a clinica...

A company is looking for a Clinical Research Associate in the Northeast region of the United States. Key Responsibilities:Conducting clinical monitoring activitiesEnsuring compliance with protocols, regulatory requirements, SOPs, and monitoring plansParticipating in site feasibility and selectionReq...

Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor's degree in a cli...

A company is looking for a Clinical Research Associate in the United States. ...

Bachelors degree with 4+ year experience as a Clinical Trials Associate; or Associate's degree with 7+ years' experience as a Clinical Trials Associate; or 10+ years clinical research experience. Participate in clinical research teams to ensure the most effective and efficient conduct of clinical re...

A company is looking for a Clinical Research Associate in the United States. ...

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. Responsible for managing the research activities at sites participating in Worldwide’s clinical...

Clinical Research Associate (Part-Time). Collaborate with Contract Research Organizations (CROs) and vendors to ensure efficient delivery of study materials and documentation to investigator sites. Minimum of 2+ years of clinical monitoring experience in oncology trials required. ...

Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...

Join Kelly FSP as a Regional Clinical Research Associate fully dedicated to a Medical Device organization!. ...

The Senior Clinical Research Associate will report to Manager, Clinical Affairs, and will play a key role to proactively support the conduct of pre-market and post-market clinical studies to ensure compliance with all the regulatory requirements. Contribute to all clinical research activities to ens...

Clinical Research Associate (CRA/Senior CRA for In-House Opportunity). Participate in providing guidelines for assessing the adequacy of potential clinical investigators and sites: including evaluating facilities, personnel, patient referral base, and adherence to Good Clinical Practices (GCP). Part...

Previous experience as a Clinical Research Coordinator or similar role. Coordinate and oversee clinical research studies from start to finish. Knowledge of clinical development processes and compliance management systems. Familiarity with clinical laboratory procedures and data collection methods. ...

The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...

Bachelors degree with 4+ year experience as a Clinical Trials Associate; or Associate’s degree with 7+ years’ experience as a Clinical Trials Associate; or 10+ years clinical research experience. Participate in clinical research teams to ensure the most effective and efficient conduct of clinical re...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor’s degree in a cli...

The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and entering clinical...

As the Clinical Research Associate, you will independently monitor clinical trial data by Good Clinical Practices (GCP), ICH, FDA, and internal standard operating procedures (SOPs). Thorough knowledge of clinical research concepts, practices, GCDMP, FDA regulations, and ICH Guidelines regarding drug...

The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and entering clinical...

As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...

Clinical Research Associate II will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor’s degree in a clinica...

Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...

Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research methodol...

As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...