Alzheimer's Trials: Full-Cycle CRC with Relocation Support

Medix™; Austin (TX); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

A leading clinical research organization is seeking a Full Cycle Clinical Research Coordinator to manage all aspects of Alzheimer's clinical trials. This role requires knowledge of GCP and FDA regulations, excellent organizational and communication skills, and a minimum of 2 years of experience in clinical trial coordination. The candidate should hold a Bachelor’s in life sciences and have proficiency in clinical systems. Full-time position with relocation assistance available.

Qualifications

• 2+ years of experience coordinating clinical trials, preferably in CNS or Alzheimer’s research.
• Knowledge of ICH-GCP and FDA regulations.
• CPR/First Aid certified or willing to obtain.

Responsibilities

• Oversee and manage all aspects of Alzheimer’s clinical trials.
• Prepare, submit, and track IRB submissions.
• Conduct study visits and administer cognitive assessments.

Skills

Organizational skills

Communication skills

Interpersonal skills

Proficiency in EDC systems

Education

Bachelor’s degree in life sciences or related field

Tools

EDC systems

CTMS

eRegulatory systems

Job description

A leading clinical research organization is seeking a Full Cycle Clinical Research Coordinator to manage all aspects of Alzheimer's clinical trials. This role requires knowledge of GCP and FDA regulations, excellent organizational and communication skills, and a minimum of 2 years of experience in clinical trial coordination. The candidate should hold a Bachelor’s in life sciences and have proficiency in clinical systems. Full-time position with relocation assistance available.