Senior CNS Clinical Research Associate | Global Trials

Worldwide Clinical Trials; North Carolina; Sur place; USD 97 000 - 193 000; Plein temps

Résumé du poste

Worldwide Clinical Trials is seeking a Clinical Research Associate to support sites across multiple therapeutic areas, including cardiovascular, metabolic, neuroscience, oncology, and rare diseases. You will manage site activities, facilitate start-up, contract and budget negotiations, and train sites to collect accurate data.

You will conduct SIVs, monitor study progress, ensure informed consent, safety reporting, and regulatory compliance.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• Willingness to travel regionally is required.

Responsabilités

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Participate in all stages of the clinical study, including site identification, start-up, regulatory documents, contracts and budgets, training, data collection, safety reporting, site maintenance, and study close-out.
• Conduct study initiation visits (SIVs).
• Ensure informed consent, safety reporting, and regulatory compliance, with most work performed remotely.

Connaissances

Interpersonal skills

Oral communication

Written communication

Organizational skills

Ability to work with little supervised

Formation

4-year university degree

Nursing Degree

Outils

CTMS

EDC Systems

Description du poste

Worldwide Clinical Trials is seeking a Clinical Research Associate to support sites across multiple therapeutic areas, including cardiovascular, metabolic, neuroscience, oncology, and rare diseases. You will manage site activities, facilitate start-up, contract and budget negotiations, and train sites to collect accurate data.

You will conduct SIVs, monitor study progress, ensure informed consent, safety reporting, and regulatory compliance.