Job Summary:
Coordinates day-to-day activities of several small scale project(s) or phases of one or more larger projects. May oversee assigned work of project staff. Works under general supervis...

Job Summary:
Manages day-to-day activities of a major segment(s) of medium to large studies or several smaller studies. May supervise project staff. Works under general supervision. Final review ...

Preferred Qualification - LVN (Licensed Vocational Nurse) Vaccine / COVID 19 Clinical Trials experience COMPANY: KAISER TITLE: LVN / Clinical Research Associate III, Vaccine Clinical Trials LOCATION: ...

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Vaccine / COVID 19 Clinical Trials experience.

Vaccine / COVID 19 Clinical Trials experience. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials.

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Vaccine / COVID 19 Clinical Trials experience.

Vaccine / COVID 19 Clinical Trials experience. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials.

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Vaccine / COVID 19 Clinical Trials experience.

Vaccine / COVID 19 Clinical Trials experience. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials.

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Vaccine / COVID 19 Clinical Trials experience.

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Minimum one (1) year of training and/or experience in ...

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Minimum one (1) year of experience in clinical trials ...

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Vaccine / COVID 19 Clinical Trials experience.

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...

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...

Collaborate with Clinical Trials Manager (CTM) and Clinical Research Associates (CRAs) to resolve clinical trial documentation issues. Responsible for clinical trials administration to ensure the most...

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Minimum one (1) year of experience in clinical trials ...

Clinical Trials Management Associate - I*. Clinical Trials Management Associate - I*,. Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is de...

Clinical Trials Management Associate – I. Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must meet all requirements for Clini...