Clinical Research Associate II

CRO Solutions; Salford; Hybrid; GBP 35,000 - 50,000; Full time

Job summary

A leading clinical research organization in the UK is seeking a Clinical Research Associate II to join their team in Salford. This hybrid position involves site selection, data management, and ensuring compliance with regulatory standards. The ideal candidate will have at least 2 years of CRA experience, a science degree, and strong communication skills. Join a passionate team dedicated to delivering high-quality clinical trials with the flexibility of working from home and in the office.

Qualifications

• 2+ years of CRA experience is essential.
• In-depth knowledge of drug development and ICH GCP.
• Ability to work independently and within a team.

Responsibilities

• Site selection, training, and management.
• Ensuring data integrity and regulatory compliance.
• Resolving data queries and conducting analyses.

Skills

Clinical trial experience

Good communication skills

Organisational skills

Excellent IT skills

Education

Bachelor's science degree or equivalent

Job description

Overview

Clinical Research Associate II An exciting opportunity working with a UK leading CRO.

CRO Solutions an IQVIA business is recruiting for an experienced CRA (CRA II) to join an existing team of established CRAs, working on a range of clinical trials. The position will be a hybrid role of office based (in our premises in Salford, Manchester) and work from home when not monitoring at study sites.

Clinical trial experience is essential for this permanent role, which would suit a well-motivated, enthusiastic and organised person who is able to work independently, as well as within an established team.

The Role

The successful candidate will be responsible for :

• Site selection, training and management
• Providing the highest quality collection and review of data and source documentation / case report forms
• Ensuring data integrity, patient safety and regulatory compliance
• Accountable for protocol compliance
• Resolving data queries
• Conducting interim analyses as required

Qualifications

Qualifications :

Ideal candidates will have 2 years of CRA experience, be educated to a Bachelors science degree or equivalent and have an in-depth knowledge and understanding of drug development / research including ICH GCP. As well as good communication and organisational skills, you will also have excellent IT skills.