KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
- Educated to Degree level (or equivalent) in life sciences and/or an area relevant to the role, with recognised management qualification or comparable work experience.
- A minimum of 10 years of prior hands-on Clinical Monitoring experience working on phase I-IV trials within the CRO/Pharmaceutical/Biotech industry.
- Minimum 15 years’ clinical research experience across the project life cycle including start-up, conduct and close out (desirable).
- Track record of three or more years leading and managing Clinical Monitoring functions, covering all monitoring activities within clinical trials from start-up to close-out, leveraging internal and external resources.
- Experience in timeline/resource/budget planning and vendor/contractor oversight.
RESPONSIBILITIES:
As part of the Clinical Monitoring Leadership Team (CMLT), oversee assigned Clinical Monitoring team to ensure delivery of high-quality deliverables, on time and in-line with customer expectations achieving a high level of customer satisfaction and profitability. Ensure all relevant protocols, project plans, SOPs and regulatory requirements are adhered to.
PHYSICAL, WORK ENVIRONMENT, TRAVEL DEMANDS:
- You must be available to travel at least 50% of the time (within the UK and internationally – including flying) based on project and business need.
- You should possess a full and valid UK driving licence with business insurance cover.
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.
Please email [email protected] 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.
