Clinical Research Associate

JR Italy; L'Aquila; In loco; EUR 35.000 - 65.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is expanding and seeks skilled Clinical Research Associates (CRAs) to join their team. This role is pivotal in ensuring the timely and quality delivery of site monitoring activities, adhering to the Site Monitoring Plan. Candidates should possess a solid understanding of ICH GCP and clinical trial regulations, along with strong communication skills. The company offers a dynamic environment where your contributions directly impact the success of global studies. If you are passionate about clinical research and eager to grow in your career, this opportunity is perfect for you.

Competenze

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

Mansioni

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

Conoscenze

Site Monitoring

Communication Skills

ICH GCP Understanding

Multitasking

Formazione

Bachelor's Degree in a Scientific Discipline

Master's Degree in a Scientific Discipline

Descrizione del lavoro

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CliniRx has a number of CRA positions available to support a global study in Q1 2025.

We are expanding rapidly and offer multiple 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 contract research organization (CRO), we provide a diverse range of 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 facing unique challenges. Our presence includes markets such as the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose:

We are seeking skilled CRAs to ensure the timely and quality delivery of site monitoring activities in line 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 quality and adherence to 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 improve technical and soft skills to enhance performance and project outcomes.

Work Relations:

1. Report to the Manager of Clinical Operations regarding project, functional, and administrative matters.
2. Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added:

Your adherence to quality standards and timelines is crucial for the efficient delivery of our projects and overall success.

Key Success Factors:

1. Timely and high-quality site monitoring activities.
2. Prompt report generation and submission to stakeholders.
3. Education: Bachelor’s or Master’s degree in a scientific discipline.
4. Experience: 1-4 years in site monitoring within clinical research.
5. Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.