Research Associate

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

Résumé du poste

A leading global contract research organization is looking for Clinical Research Associates (CRA) to ensure high-quality site monitoring for various clinical studies. The role involves managing site compliance, identifying new sites, and enhancing skills for better project outcomes. Ideal candidates will have a scientific degree and experience in clinical research.

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 adherence to quality.
• Manage sites according to the SMMP and relevant regulations.
• Assist in identifying new potential sites across various therapeutic areas.

Connaissances

Communication

Multitasking

Formation

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

Description du poste

Job Opportunity: Clinical Research Associate (CRA)

CliniRx is expanding rapidly and has multiple permanent CRA positions available on a global study basis. We are looking for candidates with a CRO background and experience across various therapeutic areas.

About Us: As a global contract research organization (CRO), we offer diverse clinical development and resource solutions, including full-service CRO and functional service provider (FSP) models. We support clinical outsourcing for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises, with a presence 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 accordance with our Site Monitoring Plan (SMP).

Key Responsibilities

1. Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
4. Continuous Skill Development: Regularly enhance technical and soft skills to improve performance and project outcomes.
5. Work Relations: Report to the Manager of Clinical Operations and collaborate with site monitoring team, site personnel, HR, site leads, and administrative staff.

Key Success Factors

• Timely and high-quality site monitoring activities
• Punctual report generation and submission

Essential Skills and Experience

• 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 and clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines