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Remote Clinical Research Associate Jobs in Georgia

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
Hr Services Research Associate - Hrsc (Remote)
By The Home Depot At Atlanta, GA, United States
The knowledge, skills and abilities typically acquired through the completion of a high school diploma and/or GED.
Associate Degree, some college education or HR experience in a shared services environment
Working knowledge of Microsoft Office Suite
Excellent written and verbal communication skills
Previous HR Service Center experience
No additional years of experience
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

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and