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

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...

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...

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 ...

We are seeking a Clinical Research Associate I (CRAI) who 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 ...

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 ...

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...

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...

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...

Excellentknowledge of Clinical Research methods andprocedures. Scor other diploma from a Clinical Researchprogram. Avalid Clinical Researchlicense. Yourexpertise and opinions shall be valuable to us which shall help usin ourresearch. ...

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...

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. ...

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...

The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I - Obstetrics & Gynecol...

Working under direct supervision, the Research Associate I performs a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. Clive Svendsen and his research group as a Research Associate I in the ...

The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator I, SLASH (Onsite). Respo...

Manage assigned projects and support Senior Project Managers and Program Managers as needed. Perform the following project management duties; develop and maintain project Management plan which includes the scope of work, project staffing plan with clear roles and responsibilities and process workflo...

Provide clinical support, and ensuring the research trials compliance within research protocols. Graduation from accredited Medical Assisting from an accredited educational program and/or Medical Assistant Certification from Board approved Medical Assistant Organization required. Part Time Research ...

The Marketing Project Coordinator is responsible for planning, organizing, and executing marketing projects. Strong project management skills, including the ability to plan, organize, and execute projects on time and within budget, and providing recap emails to ensure visibility and alignment across...

Clinical Research Coordinator (sponsor-backed trials) Highly Preferred BA/BS in a scientific discipline. We are a global Clinical Research Institute that has been conducting Clinical Trials over the last 25 years. ...

Effectively presents research findings to the Biology team. ...

Establish and maintain positive and effective relationships with clients, Construction Managers, project team, consultants/architect/engineers, subcontractors, adjacent community, trade unions, and government agencies. Review all project documents, including project submittals, RFIs, and shop drawin...

Our team is seeking one full-time Study Operations Assistant to support a large-scale military research program at the Naval Health Research Center in San Diego. The position will work closely with the Survey Operations teams to execute funded research projects that collect data from servicemembers ...

The Clinical Research Coordinator must also be able to perform clinical. Writes patient information sheet for clinical studies for submission to IRB, as well as. Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as. ...

Assisting regional research managers in the planning, execution, and management of research projects. Preference for individuals with experience in conducting research and analysis across diverse data sets. ...