Clinical Research Associate - Centivax
South San Francisco, CA 94080
About the Job
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
Source : Centivax