Clinical Research Associate: Average Salary in Palo Alto, CA in 2024

A company is looking for a Senior Clinical Research Associate to oversee clinical trial activities and ensure compliance with regulatory requirements. ...

Strong knowledge of clinical research regulations (ICH-GCP, ISO 14155, FDA, and EU). Having received their series B not too long ago, they are making great strides in the product development for their minimally invasive product and they are looking for a clinical trial manager or senior CRA to aid t...

A company is looking for a Clinical Research Associate 2 / Sr. ...

The Clinical Research Associate will provide support to the Senior Director, Clinical Operations in managing and tracking key study deliverables and milestones. Minimum 5 years of experience directly supporting oncology clinical research trials in-house at a pharmaceutical company or CRO. This posit...

Understanding of clinical research activities including tasks associated with study start up, interim monitoring, close out, data collection and central files. Clinical Research Associate experience. Support and/or lead clinical research study start up activities (includes creation of study binders,...

Clinical Research Associate (CRA) - Oncology. We are seeking a dedicated and experienced Clinical Research Associate (CRA) with a focus on Oncology to join our dynamic team. The CRA will be responsible for monitoring and managing clinical trials to ensure that they are conducted in accordance with e...

As a Clinical Research Associate, you will play a crucial role in the planning, execution, and monitoring of medium and large-sized clinical trials. They are seeking a seasoned Clinical Research Associate to join their growing team. BS/BA in relevant discipline and at least 4 years of industry exper...

Minimum of 3+ years in clinical research industry . FDA, EMA), and clinical trial processes. Perform routine monitoring visits to clinical sites according to the monitoring plan. Track subject recruitment and enrollment status at clinical sites. ...

Serving as a core member of the clinical project team and quality execution on clinical protocols according to SOPs, ICH/GCP, and departmental goals. CRAs (in house) to support their clinical studies. ...

Job Title: Senior Clinical Research Associate. Bachelor’s degree in a relevant field or a nursing degree, with 4+ years of experience in clinical research, preferably in a sponsor company, CRA, or CRO setting. Collaborate with the Study Lead and project team to ensure the quality execution of clinic...

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. We are currently looking for a Clinical Research Coordinator Associate to assist with translational research efforts. As a Clinical Research Coordinator Associate, you would coordina...

This role requires coordination with the Contract & Budget team, and collaboration with divisional and regional clinical teams, the Senior Clinical Research Associate conducts clinical trial site start-up activities related to the preparation and approval of regulatory documents, ensuring they are c...

The candidate will be required to work closely with clinical study managers, clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, contribute to clinical study reports, or...

Essential Functions of the job:• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and/or medical devices• Conduct site visits to determine protocol and regulatory compliance, and ...

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Additionally, this role will be responsible for implementing and monit...

Essential Functions of the job:• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and/or medical devices• Conduct site visits to determine protocol and regulatory compliance, and ...

Additional responsibilities: Provides technical assistance to study sites regarding the conduct of clinical research Track data report forms, reports, and documents necessary for completion of clinical study, both in-house and from participating study sites Oversees delivery and shipment of aligners...

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 works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...

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. ...

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. The Biomedical Imaging Research Institute (BIRI) is an interdisciplin...

The candidate will be required to work closely with clinical study managers, clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, contribute to clinical study reports, or...

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...

The candidate will be required to work closely with clinical study managers, clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, contribute to clinical study reports, or...

The Research Associate II works primarily in the laboratory to conduct relevant experiments and complex tasks under minimal supervision of other senior research associates or scientists. Research Associate II (Clinical NGS and RHT). Job Title: Research Associate II (Clinical NGS and RHT). The Resear...