Clinical Research Associate II

Medicines Evaluation Unit; Salford; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in Salford is seeking a Clinical Research Associate II to manage site selection and ensure data integrity in clinical trials. The ideal candidate will have at least 2 years of experience, a Bachelor's degree in a scientific field, and strong communication and IT skills. This hybrid role requires independent work and collaboration in an established team, ensuring compliance with regulatory standards and protocol adherence. This is a permanent position offering competitive benefits.

Qualifications

• Minimum 2 years of CRA experience.
• Knowledge of drug development and ICH GCP.
• Ability to work independently and in a team.

Responsibilities

• Select, train, and manage study sites.
• Ensure data integrity and compliance.
• Resolve data queries and conduct analyses.

Skills

Clinical trial experience

Communication skills

Organizational skills

IT skills

Education

Bachelor's degree in a scientific field

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.