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Clinical Monitoring Manager

2 months ago


Leeds, United Kingdom MAC Clinical Research Full time

We are seeking to appoint a Clinical Monitoring Manager to manage our Clinical Monitoring team and positively impact our progressive CRO company as we expand our clinical services outside of the UK.

Reporting to Head of Global Clinical Operations, this is a fantastic opportunity to drive the growth and development of the Clinical Monitoring teams with responsibilities for line management, process development, business development with the objective of delivering excellence across the Clinical Operations.


This is a remote based role with travel as required.


About us

MAC is a full-service, global Contract Research Organisation (CRO) providing site and patient services with complete solutions covering a wide range of therapeutic areas. Established in 1988 as one of Europe’s first-ever memory assessment centres, we have a vast and rich history becoming the UK’s neuroscience centre of excellence, expanding into a fully owned network of sites, and assuring patient recruitment.


Key Responsibilities include:

To provide line management to the Clinical Monitoring team and expert Clinical Monitoring support to MAC Clinical Research and its customers.

  • To lead and manage assigned line reports within the Clinical Monitoring team including budget, resources, vendors and CRO activities to allow the delivery of high quality, profitable and timely deliveries to MAC clients.
  • To develop best working practices and Standard Operating Procedures to deliver the portfolio of projects within the Clinical Monitoring team in line with relevant SOP’s and in accordance with ICH-GCP.


Required Qualifications, Experience, and Skills:

  • Educated to Degree level (or equivalent) in an area relevant to the role.
  • A minimum of 8 years of prior Clinical Monitoring experience within the CRO/Pharmaceutical/Biotech industry.
  • Track record of leading and managing Clinical Monitoring functions, covering all aspects of Clinical Monitoring activities within clinical trials, leveraging internal and external resources; experience in timeline/resource/budget planning and vendor/contractor oversight.
  • Excellent oral and written communication skills with proven experience of delivering successful outcomes across client, clinical and internal teams.
  • Fluent in oral and written English
  • Excellent planning, organisational and time management skills used to successfully coordinate and manage project teams to positive deliveries.
  • Advanced analytical and problem-solving ability.
  • In-depth knowledge of the global drug development process and its regulatory framework; hands-on experience within clinical trials (Phase I to IV).

BENEFITS:

  • Competitive salary in keeping with pharmaceutical industry standards and reflecting experience
  • 25 days annual leave plus bank holidays (increasing in increments to 30 days after 6 years long service)
  • Your birthday off work
  • Pension
  • Private healthcare

MAC Clinical Research invites applications from highly motivated candidates, with a desire to achieve their full potential in a fast-paced growing environment with opportunities for continued personal development. You will be working within an organisation that sees you as an investment and is keen to support you in achieving your career aspirations.

Please email maccareers@macplc.com should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.