Clinical Research Associate - onsite monitoring experience required

ICON; United Kingdom; Remote; GBP 30,000 - 50,000; Full time

Job summary

A leading global clinical research organization is seeking a Clinical Research Associate. The role involves managing clinical trials and ensuring compliance with protocols. Candidates should possess experience in the pharmaceutical sector and be ready for travel. ICON offers a competitive salary and extensive benefits.

Benefits

Health insurance

Retirement plans

Flexible benefits

Life assurance

Employee Assistance Programme

Competitive salary

Diverse culture

Annual leave

Qualifications

• Up to 12 months pharmaceutical industry or relevant experience.
• Right to work in the UK.
• Minimum 12 months monitoring experience.

Responsibilities

• Conduct site selection, manage study sites, and perform site initiation.
• Negotiate investigator remuneration and prepare financial contracts.

Skills

Knowledge of drug development process

Monitoring experience

Knowledge of GCP/ICH, FDA, EMEA standards

Job description

Title - Clinical Research Associate

Location - UK, nationwide travel

Sponsor dedicated

As a CRA, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Working fully embedded within a global healthcare company, you will be responsible for the following activities:

Your responsibilities include, but are not limited to:

1. Allocation, initiation, and conduct of trials: Conducts site selection, manages study sites, performs site initiation, monitoring, and closeout activities, ensures compliance with protocols and regulations, documents activities, collaborates with stakeholders, and manages data query resolution.
2. Negotiates investigator remuneration and prepares financial contracts.

You will need the following:

• Right to work in the UK
• Up to 12 months pharmaceutical industry or relevant experience (NHS or Academic)
• Good knowledge of drug development process and clinical trials
• Knowledge of international standards (GCP/ICH, FDA, EMEA)
• Minimum 12 months monitoring experience

Important for the role:

• Ability to travel domestically and possibly internationally; minimum 50% overnight travel required.

What ICON can offer you:

Competitive salary, diverse culture, benefits including annual leave, health insurance, retirement plans, Employee Assistance Programme, life assurance, and flexible benefits.

Visit our careers website for more: https://careers.iconplc.com/benefits

ICON is committed to inclusion & belonging, providing an accessible environment, and equal opportunity employment. For accommodations, contact us through the provided link.

We encourage you to apply even if you’re unsure about meeting all requirements, as you may still be a good fit.