Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the ...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Parexel is proud to be a leading Clinical Research Organization with c...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Have a question? A clinical research leader, project team member, tech...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Parexel is proud to be a leading Clinical Research Organization with c...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the ...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Parexel is proud to be a leading Clinical Research Organization with c...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Have a question? A clinical research leader, project team member, tech...

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the ...

Pharmacovigilance (GVP), Clinical Research (GCP), Regulatory affairs, quality assurance and GxP auditing. Leveraging our established research, development, and commercial capability and infrastructure...

Strong clinical research and program management experienced in leading cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory, CMC or other drug development related f...

Strong clinical research and program management experienced in leading cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory, CMC or other drug development related f...

Strong clinical research and program management experienced in leading cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory, CMC or other drug development related f...

Strong clinical research and program management experienced in leading cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory, CMC or other drug development related f...

Pharmacovigilance (GVP), Clinical Research (GCP), Regulatory affairs, quality assurance and GxP auditing. Leveraging our established research, development, and commercial capability and infrastructure...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...

Working with a highly experienced team of clinical research professionals. High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical researc...

The Clinical Research Scientist participates in the development, strategic planning, and execution of clinical development programs in collaboration with other clinical development team members, inclu...

Working with a highly experienced team of clinical research professionals. High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical researc...

As a Lead Clinical Research Associate (CRA) at Bicara Therapeutics, you will support the planning and execution of clinical trials to ensure they meet regulatory standards and timelines. Minimum of 2 ...

Minimum of 2 years of experience as a Clinical Research Associate or in clinical trial management, with a focus on site management and trial monitoring of Phase I, II, and II studies; oncology experie...

Strong clinical research and program management experienced in leading cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory, CMC or other drug development related f...

Minimum of 2 years of experience as a Clinical Research Associate or in clinical trial management, with a focus on site management and trial monitoring of Phase I, II, and II studies; oncology experie...

Minimum of 2 years of experience as a Clinical Research Associate or in clinical trial management, with a focus on site management and trial monitoring of Phase I, II, and II studies; oncology experie...

THE IN-HOUSE CLINICAL RESEARCH ASSOCIATE (CRA) ROLE. The In-house CRA is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval throu...

THE IN-HOUSE CLINICAL RESEARCH ASSOCIATE (CRA) ROLE. The In-house CRA is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval throu...

THE IN-HOUSE CLINICAL RESEARCH ASSOCIATE (CRA) ROLE. The In-house CRA is an important member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval throu...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...

Experienced Clinical Research Associates- a. We are rapidly growing and are seeking experienced Clinical Research Associates to join our team!. Candidates must have at minimum a Bachelors degree in a ...

The Clinical Research Associate I (CRA I) works under general supervision to enroll eligible patients to clinical research protocols and manage data collection and regulatory submissions for multiple ...

We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associ...

We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associ...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and monitoring of multiple oncology trials. The Clinical Research Associate II should also possess:. A Cli...

The Multi-Center Clinical Research Associate/Monitor III (CRA III) works independently, under minimal supervision, to initiate, manage and navigate a portfolio of Investigator-initiated, multi-center ...

The Multi-Center Clinical Research Associate/Monitor III (CRA III) works independently, under minimal supervision, to initiate, manage and navigate a portfolio of Investigator-initiated, multi-center ...

The Multi-Center Clinical Research Associate/Monitor III (CRA III) works independently, under minimal supervision, to initiate, manage and navigate a portfolio of Investigator-initiated, multi-center ...

The Clinical Research Associate I (CRA I) works under general supervision to enroll eligible patients to clinical research protocols and manage data collection and regulatory submissions for multiple ...