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Clinical Study Manager

2 months ago

London, Greater London, United Kingdom MAC Clinical Research Full time
About the Role

We are seeking a highly skilled and experienced Clinical Study Manager to join our team at MAC Clinical Research. As a Clinical Study Manager, you will be responsible for managing our Clinical Monitoring team and contributing to the growth and development of our clinical services.

Key Responsibilities
  • Provide line management to the Clinical Monitoring team and expert Clinical Monitoring support to MAC Clinical Research and its customers.
  • Lead and manage assigned line reports within the Clinical Monitoring team, including budget, resources, vendors, and CRO activities to deliver high-quality, profitable, and timely deliveries to MAC clients.
  • Develop best working practices and Standard Operating Procedures to deliver the portfolio of projects within the Clinical Monitoring team in line with relevant SOPs and in accordance with ICH-GCP.
Requirements
  • 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.
  • Fluent in oral and written English.
  • Excellent planning, organizational, and time management skills used to successfully coordinate and manage project teams to positive deliveries.
  • In-depth knowledge of the global drug development process and its regulatory framework; hands-on experience within clinical trials (Phase I to IV).
What We Offer
  • 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.