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Clinical Research Associate | Research Associate in Research Job at Centivax in South San Francisc1

This listing was posted on The Resumator.

Clinical Research Associate

Location:
South San Francisco, CA
Description:

Responsibilities: As a vital member of our clinical team, the Clinical Research Associate will be responsible for conducting Phase I-IV single or multi-center studies in adherence to Federal Regulations and ICH guidelines. Key responsibilities include: Collaborating with senior staff in planning study conduct. Designing case report forms (CRFs) and managing Contract Research. Organization (CRO) selection. Selecting and training investigator sites, planning and organizing study meetings. Evaluating, selecting, and training new study investigators. Writing and assembling submissions related to study protocols. Monitoring investigational sites to ensure protocol adherence. Ensuring timely enrollment of patients and retrieval of CRFs from study sites. Processing CRFs, including data cleanup and classification of data. Completing study summaries and reports. Experience: The ideal candidate should possess a minimum of 2 years of experience in clinical research monitoring. Key qualifications include: Proven experience in the successful execution and monitoring of clinical trials. Familiarity with Federal Regulations and ICH guidelines. Strong attention to detail and organizational skills. Ability to work effectively within a collaborative team environment. Experience with vaccines against infectious diseases clinical trials highly desired but not absolutely necessary. Education: A minimum of an Associate degree is required, but preference will be given to candidates with a Bachelor's degree. Additionally, candidates should have at least 2 years of monitoring experience with preference on vaccines against infectious diseases clinical trials. Powered by JazzHR
Company:
Centivax
Posted:
January 12 on The Resumator
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