CRA Sponsor Dedicated Belgium

Resourcing Life Science; Town of Belgium (WI); On-site; USD 49,000 - 76,000; Full time

Job summary

A global clinical research organization is seeking a CRA / Clinical Research Associate Sponsor Dedicated in Belgium. The role involves monitoring clinical studies (phases II-III), ensuring compliance with Good Clinical Practices, and working closely with investigators. Candidates should have a Bachelor's in life science and at least one year of relevant CRA experience. Fluent English, French, and Dutch are required.

Qualifications

• Minimum 1 year monitoring experience as CRA within a CRO, Pharma, Biotech.
• Experience in commercial studies.
• Experience with site initiation and close out.
• Experience in clinical studies phase II-III.
• A full clean driver's license.
• Fluent English, French and Dutch.
• Excellent communication skills.
• Full clean driver's license.

Responsibilities

• Monitor clinical studies in phases II-III.
• Ensure adherence to Good Clinical Practices and compliance.
• Identify, qualify, and initiate investigators and their sites.
• Supervise study conduct according to GCP requirements.

Skills

Monitoring clinical studies

Fluent English

Fluent French

Fluent Dutch

Excellent communication skills

Communication skills

Driver's license

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 Sponsor Dedicated in Belgium

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 Belgium
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• Fluent English & French & Dutch
• 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]

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