Clinical And Scientific - Research Scientist I
By Saviance At Johns Creek, GA, United States

Job Description: Major Accountabilities Performs polymer formulation and engineering in a research and development environment with minimum supervision Use relevant statistical techniques and ...

Clinical Research Associate (Cra)
By Peachtree BioResearch Solutions At Atlanta, GA, United States
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
Research Associate I/Ii
By Aruna Bio, Inc. At Athens, GA, United States
·Work in a laboratory setting with knowledge of basic chemical and biological safety procedures
·MS/BS in Life Sciences with 0-2 years of relevant experience is required
·Mammalian cell culture experience with aseptic technique is required
·Experience in performing molecular and biochemical assays is preferred
·Experience with handling mice and/or rats is preferred
·Experience with biological therapeutics, especially extracellular vesicles is a plus
Sr. Clinical Research Qc Associate
By Clinilabs At , Eatontown, 07724, Nj
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.
Clinical Research Associate Ii
By Labcorp At Atlanta, GA, United States
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