Clinical Research Associate

JR France; Ivry-sur-Seine; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading global CRO seeks skilled Clinical Research Associates (CRAs) for remote positions. Candidates should possess a scientific degree and experience in site monitoring. The role focuses on ensuring high-quality delivery of site monitoring activities and compliance with regulations.

Qualifications

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

Responsabilités

• Deliver on the Site Monitoring Plan and ensure quality adherence.
• Assist in identifying new sites across therapeutic areas.
• Regularly improve technical and soft skills.

Connaissances

Communication

Multitasking

Ability to work under pressure

Formation

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

Description du poste

Client:

CliniRx

Location:

Online / Remote

Job Category:

Other

EU work permit required:

Yes

Job Reference:

579201409589706752327664

Job Views:

3

Posted:

16.05.2025

Job Description:

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

Ideally, candidates will have a CRO background with experience across various therapeutic areas.

As a global CRO, we provide diverse clinical development and resource solutions, supporting biotech and pharmaceutical companies worldwide, with presence in key markets including 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 accordance with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the Site Monitoring Plan: Understand the SMMP, study protocol, and project plan to ensure quality and adherence to timelines.
• Site Management Compliance: Manage sites per the SMMP and regulations to minimize QA audit observations.
• Site Identification: Assist in identifying new sites across 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 site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added:

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

Key Success Factors:

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

Additional Notes:

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