Associate Clinical Research Specialist Jobs in Georgia

Work closely with the Site Management team and sponsor stakeholders so you can plan and manage your work most effectively

Work with Peachtree's Data Management team and sites to ensure all queries are resolved

1-5 years of experience working on clinical trials (CRO or Sponsor) as either a coordinator or CRA I

Experience with CNS, rare disease and/or oncology studies preferred

Experience working in a CTMS and EDC system

Excellent organizational and critical thinking skills

Provide support (e.g. data entry, filing, QC, etc…) to CRU personnel and other Clinilabs personnel ad requested and needed.

Manage and track project timelines and quality issues.

Must have related experience for at least five years.

Must possess excellent clerical, strong computer and good interpersonal skills.

Reading and understanding study protocols.

Communicate with all operational departments regarding project status/issues.

Perform project management activities for identified projects including resource planning, timelines and milestone management

10+ years of overall experience, or an equivalent combination of education and experience

Some knowledge of CDISC requirements preferred

Minimum of at least 1 year of Onsite Clinical Monitoring experience along with at leas

Effectively communicate statistical concepts and results to audiences with various statistical knowledge

Previous experience of leading studies as a Biostatistician in a CRO or at a medical device or pharma company required