Clinical Research Associate

JR France; Île-de-France; Sur place; EUR 35 000 - 60 000; Plein temps

Résumé du poste

A global CRO is expanding and seeks skilled Clinical Research Associates (CRAs) for site monitoring activities. This role requires a Bachelor's or Master's in a scientific discipline and offers a chance to work across therapeutic areas while supporting biotech and pharmaceutical companies globally, ensuring quality and compliance throughout clinical trials.

Qualifications

• 1-4 years in site monitoring within clinical research.
• Analysis and understanding of clinical trial regulations.

Responsabilités

• Ensure timely and qualitative site monitoring activities.
• Manage sites according to regulations.
• Assist in identifying new sites to expand the network.

Connaissances

Knowledge of ICH GCP

Excellent communication

Multitasking

Ability to meet deadlines

Formation

Bachelor's or Master's in a scientific discipline

Description du poste

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Client:

CliniRx

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

482727675945811968032767

Job Views:

1

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

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

Candidates should have a CRO background with experience across various therapeutic areas. As a global CRO, we provide clinical development and resource solutions, supporting biotech and pharmaceutical companies worldwide, with offices in the USA, UK, Netherlands, Spain, Hong Kong, India, and Australia.

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Primary Purpose: We seek skilled CRAs to ensure timely and qualitative site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the SMP: 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 regulations to minimize QA audit findings.
• Site Identification: Assist in identifying new sites across therapeutic areas to expand our network.
• Skill Development: Continuously improve technical and soft skills to enhance performance.

Work Relations:

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

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

Key Success Factors:

• High-quality and timely site monitoring.
• Prompt reporting to stakeholders.
• Education: Bachelor's or Master's in a scientific discipline.
• Experience: 1-4 years in site monitoring within clinical research.
• Skills: Knowledge of ICH GCP, clinical trial regulations, excellent communication, multitasking, and ability to meet deadlines.