Clinical Research Associate

JR France; Saint-Étienne; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

CliniRx is seeking skilled Clinical Research Associates (CRAs) to join their expanding team. Ideal candidates will have a CRO background and experience in clinical site monitoring. This role involves ensuring quality and timely site monitoring activities, collaborating with various teams, and continuous skill development.

Qualifications

• 1-4 years in clinical site monitoring.
• Strong knowledge of ICH GCP and clinical trial regulations.

Responsabilités

• Ensure timely and high-quality delivery of site monitoring activities.
• Manage sites according to the Site Monitoring Master Plan.
• Assist in identifying new potential sites across various therapeutic areas.

Connaissances

Communication

Multitasking

Ability to work under pressure

Formation

Bachelor’s or Master’s degree in a scientific discipline

Description du poste

Social network you want to login/join with:

col-narrow-left

Client:

CliniRx

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

579201409589706752327635

Job Views:

4

Posted:

16.05.2025

col-wide

Job Description:

CliniRx has multiple CRA positions available. We are expanding rapidly and offer several permanent opportunities to join us on a global study.

Ideal candidates will have a CRO background with experience across multiple therapeutic areas.

As a global CRO, we provide diverse clinical development and resource solutions, supporting emerging biotech and pharmaceutical companies worldwide, with operations in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

------------------------------------------------------------

Primary Purpose: We seek skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure quality and timeliness.
• Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize QA audit findings.
• Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our network.
• Continuous Skill Development: Regularly improve technical and soft skills to enhance performance and project outcomes.

Work Relations:

• Report to the Manager of Clinical Operations.
• Collaborate with the monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added: Your commitment to quality and timelines is crucial for project success.

Key Success Factors:

• Timely and high-quality site monitoring activities.
• Prompt report generation and submission.
• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years in clinical site monitoring.
• Skills: Strong knowledge of ICH GCP, clinical trial regulations, excellent communication, multitasking, and ability to work under pressure.