Lead Clinical Research Associate – Spain

Resourcing Life Science; España; On-site; PHP 3,693,000 - 5,327,000; Full time

Job summary

A global clinical research organization is looking for a Lead CRA / Clinical Research Associate in Spain. The role involves monitoring clinical studies in phases II-III, ensuring compliance with Good Clinical Practices, and supervising study conduct. Candidates should have a Bachelor degree in life-science, at least one year of monitoring experience, and be fluent in English and Spanish. This position is crucial for the management of clinical trials and offers an excellent opportunity to grow in the field.

Qualifications

• Minimum 1 year monitoring experience as CRA within a CRO, Pharma, or Biotech in Spain.
• Experience in commercial studies.
• Experience with site initiation and site close-out.
• Experience with site initiation and close-out.
• Fluent in English and Spanish; strong communication skills.
• Valid driver's license.

Responsibilities

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

Skills

Monitoring clinical studies

Communication skills

Fluent in English

Fluent in Spanish

Fluent English & Spanish

Valid 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 Lead CRA / Clinical Research Associate in Spain

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