Clinical Research Associate – Hungary

Resourcing Life Science; Hungary (CT); On-site; USD 35,587 - 59,312; Full time

Job summary

A global CRO firm is seeking a Clinical Research Associate in Hungary to monitor clinical studies in phases II-III. Responsibilities include ensuring compliance with Good Clinical Practices, identifying investigators, and supervising study conduct according to GCP requirements. Candidates must hold a Bachelor's degree in life-science, have at least 1 year of monitoring experience, and possess excellent communication skills. The role demands fluent English proficiency and a full clean driver's license.

Qualifications

• Minimum 1 year monitoring experience as CRA within a CRO, Pharma, Biotech.
• Experience in commercial studies, site initiation, site close out.
• Experience in clinical studies phase II-III.

Responsibilities

• Monitoring clinical studies in phases II-III.
• Assuring adherence to Good Clinical Practices and compliance with all study procedures.
• Identification, qualification, and initiation of investigators and their sites.

Skills

Monitoring clinical studies

Adherence to Good Clinical Practices

Excellent communication skills

Fluent English

Education

Bachelor degree in life-science

Job description

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate in Hungary

Job Overview

• 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.

Key Requirements

• Bachelor degree in life-science
• Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Germany
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• Fluent English
• Excellent communication skills
• A full clean drivers license
• FTE: 1.0

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email [e-mail]