Senior CRA — Metabolic Trials & Global Sites

Worldwide Clinical Trials; Louisiana (MO); On-site; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate to oversee research activities at participating sites across diverse therapeutic areas. You will handle site initiation, regulatory documents, contracts, budgets, and data reporting, while coordinating remote site management and ensuring safety and regulatory compliance.

The role requires 5+ years as a CRA, a 4-year degree or nursing degree, metabolic/ obesity experience preferred, and willingness to travel regionally within the

Qualifications

• Strong interpersonal and written communication skills in English.
• Excellent organizational skills and attention to detail.
• Ability to work with minimal supervision and manage multiple sites.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Identify potential sites, start-up activities, regulatory documents, contracts and budgets, and site training.
• Conduct study initiation visits (SIVs) and ensure regulatory compliance across sites; coordinate site activities remotely where possible.

Skills

Communication skills

Organizational skills

Independence

English proficiency

Education

Bachelor's degree or Nursing Degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate to oversee research activities at participating sites across diverse therapeutic areas. You will handle site initiation, regulatory documents, contracts, budgets, and data reporting, while coordinating remote site management and ensuring safety and regulatory compliance.

The role requires 5+ years as a CRA, a 4-year degree or nursing degree, metabolic/ obesity experience preferred, and willingness to travel regionally within the