Clinical Research Associate

CRO-Solutions® Ltd.; Manchester; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in Manchester is seeking an experienced CRA II to join their team. The role involves site selection, data collection, and ensuring regulatory compliance in a hybrid working arrangement. The ideal candidate will have a Bachelor’s degree, at least 2 years of experience in clinical trials, and strong communication and organizational skills. Benefits include a competitive salary, career progression, and generous annual leave.

Benefits

Competitive salary

Career progression opportunities

29 days annual leave plus Bank Holidays

Attractive company pension scheme

Generous annual bonus

Free on-site parking

Qualifications

• 2 years of CRA experience required.
• In-depth knowledge of drug development/research including ICH GCP is necessary.
• Ability to work independently and as part of a team.

Responsibilities

• Site selection, training, and management.
• Ensure data integrity, patient safety, and regulatory compliance.
• Conduct interim analyses as required.

Skills

Clinical trial experience

Communication skills

Organisational skills

IT skills using MS Office

Education

Bachelor’s science degree or equivalent

Job description

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
• Conducting interim analyses as required

Qualifications:

Ideal candidates will have 2 years of CRA experience, be educated to a Bachelor’s 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 using MS Office.

CRO-Solutions will offer you…….

• Competitive salary, dependent on experience.
• Immediate start
• Career progression opportunities
• 29 days annual leave plus Bank Holidays, rising to 33 days after 5 years’ service
• Attractive company pension scheme
• Generous annual bonus
• Free on-site parking

NO AGENCIES PLEASE

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