Clinical Planning Co-ordinator

Medicines Evaluation Unit Ltd; Manchester; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading clinical trials organization in Manchester is looking for a Clinical Planning Co-ordinator to support the planning and execution of clinical trials. The successful candidate will assist with scheduling, documentation preparation, and participant visits, ensuring compliance with standards. The role offers 29 days annual leave, a company pension scheme, and a generous bonus plan. Ideal for those keen on clinical research and proactive team collaboration.

Benefits

29 days annual leave plus bank holidays

Company pension scheme

Generous annual bonus

Healthcare plan after qualifying period

Free secure on-site parking

Qualifications

• Pro-active and well-organised individual.
• Commitment to high standards in clinical research.

Responsibilities

• Support clinical trial planning and execution.
• Assist with daily scheduling of staff and participant visits.
• Prepare and maintain protocol-compliant source documentation.
• Provide support during clinical activities.
• Help maintain participant confidentiality.

Skills

Strong organisational and communication skills

Attention to detail

Ability to work well in a team

Interest in clinical research

Job description

Clinical Planning Co-ordinator – An exciting role to join a continually expanding early phase clinical trials company working with some of the most distinguished domestic and global pharmaceutical companies.

A stimulating and rewarding career pathway for anyone looking to work within our busy clinical trials as a pro-active and well-organised Clinical Planning Co-ordinator, to join our team and contribute to the successful delivery of clinical trials. In this role, you will help co-ordinate staff scheduling, resource planning, documentation preparation, and supporting participant visits – all while ensuring compliance with regulatory standard and protocol requirements.

The role…

• Support clinical trial planning and execution as part of a multidisciplinary team
• Assist with daily scheduling of staff and participant visits
• Prepare and maintain accurate, protocol-compliant source documentation
• Provide practical, on-the-ground support during clinical activities
• Help maintain participant confidentiality and assist with study procedures
• Follow ICH-GCP, EU/UK clinical trial regulations, and internal SOPs

What We’re Looking For:

• Strong organisational and communication skills
• Attention to detail and a willingness to learn
• Ability to work well in a team and adapt in a dynamic environment
• Interest in clinical research and a commitment to high standards

MEU will offer you….

• 29 days annual leave plus bank holidays, increasing to 33 days after 5 years’ service
• Company pension scheme
• Generous annual bonus and healthcare plan after qualifying period
• Free secure on-site parking

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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.

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CRO-Solutions® is our sister company to Medicines Evaluation Unit Ltd. Located at Salford Quays, CRO-Solutions® has the ability to offer a single site solution for all your clinical trial needs.