Clinical Research Associate – Phase II/III (USA)

Resourcing Life Science Ltd.; United States; On-site; USD 65,000 - 90,000; Full time

Job summary

Resourcing Life Science Ltd. is seeking a Clinical Research Associate (CRA) in the USA to monitor multicenter studies in phases II-III. The role requires ensuring GCP compliance, investigator integrity, and adherence to study procedures across sites.

The successful candidate will identify and initiate investigators, supervise study conduct, and manage site performance in accordance with regulatory requirements and study protocols.

Qualifications

• Bachelor degree in life sciences.
• At least 1 year monitoring experience as CRA in USA.
• Experience in commercial studies.
• Experience with site initiation and site close-out.
• Experience in clinical studies phase II-III.
• Fluent English and German.
• Valid driver's license.
• FTE: 1.0

Responsibilities

• Monitoring clinical studies in phases II-III.
• Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
• Identification, qualification and initiation of investigators and their sites.
• Supervising study conduct according to GCP requirements and all applicable laws.

Skills

Monitoring

GCP compliance

Site initiation

Communication skills

Fluent English

German language

Education

Bachelor's in Life Sciences

Job description

Resourcing Life Science Ltd. is seeking a Clinical Research Associate (CRA) in the USA to monitor multicenter studies in phases II-III. The role requires ensuring GCP compliance, investigator integrity, and adherence to study procedures across sites.

The successful candidate will identify and initiate investigators, supervise study conduct, and manage site performance in accordance with regulatory requirements and study protocols.