Clinical Research Associate (12-Month Maternity Cover)

CRO-Solutions® Ltd.; Manchester; Hybrid; GBP 30,000 - 40,000; Full time

Job summary

A clinical research organization in Manchester is looking for a Clinical Research Associate for a 12-month maternity cover. This hybrid position combines office-based and remote work, requiring at least 1 year of clinical trial experience. Responsibilities include site selection and data integrity. Ideal candidates will have a Bachelor's degree and strong communication skills. Competitive salary and opportunities for career progression are provided.

Benefits

Competitive salary

Career progression opportunities

Attractive pension scheme

Generous annual bonus

29 days annual leave

Qualifications

• At least 1 year of Clinical Research Associate experience.
• Strong knowledge of drug development/research including ICH GCP.
• Ability to work independently and in a team.

Responsibilities

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

Skills

Clinical trial management

Data integrity

Communication skills

Organizational skills

IT skills (MS Office)

Education

Bachelor’s degree in a scientific field

Job description

Clinical Research Associate (12-Month Maternity Cover)

CRO-Solutions®, an IQVIA business is recruiting for a 12-month maternity cover CRA I position 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 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 at least 1 year 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
• Potential to make role permanent after completion of cover
• 29 days annual leave plus Bank Holidays, (rising to 33 days after 5 years’ service)
• Attractive company pension scheme
• Generous annual bonus
• Free on>

NO AGENCIES PLEASE

Data Protection

The personal data you provide for this application and otherwise as part of the recruitment process will be held and processed for the purpose of the selection processes and any other purpose as reasonably required of Medicine Evaluations Ltd and in connection with any subsequent employment or placement, unless otherwise stated. We will ensure that personal information is kept secure and shall use it for no other purposes. The personal data will be controlled by or on behalf of Medicine Evaluations Ltd. in full accordance with the Data Protection Act 1998, any subsequent amendments and all other applicable laws. Your personal data shall be stored exclusively in the UK for up to 6 years. I have read and accept the above statement and confirm that the details which I have provided in all sections of the application form are, to the best of my knowledge, true and correct.

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