In-House Clinical Research Associate: Trial Docs

Inhouse Clinical Research Associate role at NovotechAbout the RoleThe Inhouse Clinical Research Associate (IHCRA) provides in‑house administrative support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs.ResponsibilitiesSupport the Clinical Research Associates...

Inhouse Clinical Research Associaterole atNovotechAbout the Role The Inhouse Clinical Research Associate (IHCRA) provides in‑house administrative support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs.ResponsibilitiesSupport the Clinical Research Associates...

Join to apply for the Clinical Research Associate role at MedpaceContinue with Google Continue with GoogleJoin to apply for the Clinical Research Associate role at MedpaceThe Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference...

Join to apply for theClinical Research Associaterole atMedpace Continue with Google Continue with Google Join to apply for theClinical Research Associaterole atMedpace The Clinical Research Associate position at Medpace offers the unique opportunity to have anexciting careerin the research of drug and medical device development whilemaking a differencein the...

A clinical research firm in Italy is seeking a Clinical Research Associate to manage recruitment for investigators and monitor clinical sites. The candidate will conduct submissions, ensure compliance, and act as a primary contact for regulations. Must have excellent knowledge of the clinical trial process and be fluent in English and Italian. The role...

As a Clinical Research Associate you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring clinical sites, maintenance of study files, conduct of pre‑study, initiation visits, regular visits and close‑out visits, and liaison with vendors...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate at PSI Italy...

Company DescriptionPSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job Description As a Clinical Research Associate at PSI Italy you...

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential Functions• Complete appropriate therapeutic, protocol and clinical research...