Clinical Research Associate (CRA) – Erectile Dysfunction (ED) Clinical Trials. Clinical Research Associate (CRA). CROs, sponsors, or high-volume research sites.

Clinical Research Associate (CRA) – Erectile Dysfunction (ED) Clinical Trials. Clinical Research Associate (CRA). CROs, sponsors, or high-volume research sites.

Bachelor's degree in a science and/or engineering field preferred or any Bachelor's degree and 2+ years of clinical research experience. Assists with study tasks under the supervision of Investigator-...

Assists in the preparation and documentation of the Fair Market Value (FMV) Analysis of research budgets for IIR, MACS, and Collaborative Research studies. Bachelor's degree in a science and/or engine...

Clinical Research Associate 2064742. Join our client as the inaugural in-house Clinical Research Associate to oversee quality and patient safety, coordinating with a CRO and facilitating daily study o...

Clinical Research Associate 2064742. Join our client as the inaugural in-house Clinical Research Associate to oversee quality and patient safety, coordinating with a CRO and facilitating daily study o...

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...

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...

Select and manage contract research organizations (CROs) to support non-clinical development programs Design and manage non-GLP and GLP pre-clinical studies (pharmacology, PK/PD, DRF, toxicology) cond...

Select and manage contract research organizations (CROs) to support non-clinical development programs Design and manage non-GLP and GLP pre-clinical studies (pharmacology, PK/PD, DRF, toxicology) cond...

THE IN-HOUSE CLINICAL RESEARCH ASSOCIATE (CRA) ROLE. In-house CRAs manage and support clinical sites from site approval through close-out. In-house CRAs work closely with field CRAs and Clinical Proje...

THE IN-HOUSE CLINICAL RESEARCH ASSOCIATE (CRA) ROLE. In-house CRAs manage and support clinical sites from site approval through close-out. In-house CRAs work closely with field CRAs and Clinical Proje...

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...

As the Senior Clinical Research Associate (CRA) you will be a key player in managing clinical trials from start to finish, ensuring that projects are executed efficiently, within budget, and in compli...

As the Senior Clinical Research Associate (CRA) you will be a key player in managing clinical trials from start to finish, ensuring that projects are executed efficiently, within budget, and in compli...

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 ...

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 ...

Clinical Research Associate-(3292572). The Clinical Research Associate (CRA) will assist with our study on Mindful Self-Compassion as a treatment for PTSD. Working knowledge of clinical research proto...

Clinical Research Associate-(3292572). The Clinical Research Associate (CRA) will assist with our study on Mindful Self-Compassion as a treatment for PTSD. Working knowledge of clinical research proto...

Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. Includes Clinical roles focused on research projects. Exp...

Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. Includes Clinical roles focused on research projects. Exp...

A Clinical Research Associate II may assist with the training and orientation of new staff members. PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and mo...

The Clinical Research Associate II should also possess:. A Clinical Research Associate II may assist with the training and orientation of new staff members. Clinical Research Associate II---Cancer Cen...

Clinical Research Associate II---Cancer Center Protocol Office-(3293250). PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and monitoring of multiple oncol...

PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and monitoring of multiple oncology trials. A Clinical Research Associate II may assist with the training ...

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 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 candidate will also manage a team of clinical research coordinators/research assistants to ensure efficient functioning of the clinical and translational research infrastructure. The candidate wil...

The candidate will also manage a team of clinical research coordinators/research assistants to ensure efficient functioning of the clinical and translational research infrastructure. The candidate wil...

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 ...

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 ...

The Cancer Center Protocol Office is a centralized clinical research office that supports clinical researchers in all disciplines within the Cancer Center. The Associate Manager provides first-line su...

The Cancer Center Protocol Office is a centralized clinical research office that supports clinical researchers in all disciplines within the Cancer Center. The Associate Manager provides first-line su...

Oversee investigator-initiated and grant funded clinical trials including development of protocols/budgets, support the contract process, and coordinate correlative sample processing Lead process impr...

Oversee investigator-initiated and grant funded clinical trials including development of protocols/budgets, support the contract process, and coordinate correlative sample processing Lead process impr...