Clinical Research Coordinator (10034)

Responsibilities

• Coordinates, assists, and implements clinical research projects.
• Performs duties associated with coordinating study initiation, investigators’ training, and implementing study protocols.
• Supports, facilitates, and organizes daily clinical trial activities.
• Works under the direction of the principal investigator (PI).
• Manages the day-to-day clinical operations activities, overseeing and executing delegated tasks to appropriate parties.
• Collaborates with the department, sponsor, and institution to address compliance, finances, and personnel issues.

Requirements

• Bachelor’s degree in a related field.
• Minimum of 2 years of relevant experience in clinical research or related field.
• Experience with regulatory requirements and Good Clinical Practice (GCP).
• Strong organizational and communication skills.
• Ability to manage multiple projects simultaneously.
• Proficiency in Microsoft Office Suite.

Qualifications

• Current CPR certification.
• Knowledge of HIPAA regulations.
• Basic understanding of statistical analysis.

Skills

• Excellent verbal and written communication skills.
• Strong attention to detail.
• Ability to work independently and as part of a team.
• Proficient in data management software (e.g., REDCap).

Benefits

• Health insurance coverage.
• Flexible work schedule.
• Professional development opportunities.

Pay

• $50,000 - $60,000 annually.

Schedule

• Mon – Fri: 09:00AM – 06:00PM

Location

1236 Poydras St, Ste - 301A, New Orleans, LA 70113

Contact

+1 (504) 420-7800