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    • Conducting audits on clinical trials, systems and service providers.
    • Excellent knowledge of the regulations governing clinical trials and auditing experience…
    • Experience contributing to product development, clinical research or evidence generation.
    • Identify opportunities for collaboration, education, research and…
    • Key requirements: * Experience in patient care - 2+ years minimum * Experience in clinical evaluation, clinical data assessment, and medical statistics -…
    • Collaboration with international clinical research teams.
    • Experience delivering early-phase clinical trials.
    • Exposure to innovative early-phase clinical trials.
    • You will bring substantial experience of complex research, data or digital services; confidence working with real-world health data, clinical informatics and…
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    • Proven experience in clinical research or public health initiatives related to workplace health.
    • Provide clinical oversight for health surveillance.
    • Responsible for all scientific and operational statistical work for assigned clinical trials and observational studies, or real world data investigations.
    • Proficiency in clinical systems (Veeva Vault, CTIS, RIM, etc.).
    • Demonstrated experience in clinical trial start-up, regulatory submissions, and cross-functional…
    • Oversee the forecasting and maintenance of supplies (including IMP) needed to ensure sites have the necessary resources to run clinical studies.
    • Extensive experience in clinical data management or a related function.
    • Hands-on experience managing data for clinical trials (e.g., CRF design, query…
    • As a Research Finance Coordinator, you will provide high-quality financial and administrative support for clinical research activity within the Joint Research…
    • To work according to the principles of Good Clinical Practice & research governance standards for clinical research studies.
    • Your primary responsibility will be managing a portfolio of research projects and providing outstanding leadership and line management for the research team, in…
    • The post holder will be involved in all aspects that are key to our service development and expected to participate in activities such as equipment validations,…
    • Demonstrate a good understanding of the research environment to support the delivery and development of research portfolios in order to take responsibility for…

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clinical trial
Monitoring Manager and Quality Associate
44 Cumberland Avenue, London NW10 7EW
£44,500 - £50,000 a year
Permanent, Full-time

Job details

£44,500 - £50,000 a year
Permanent, Full-time
44 Cumberland Avenue, London NW10 7EW

Full job description

At Nucleus Network, our work helps move new medicines from lab to life. As the only dedicated global phase 1 clinical trials specialist with facilities across Australia, the United Kingdom, and the United States, we are committed to advancing medicine and improving lives by attracting exceptional talent.

Our values - Care, Innovation and Collaboration - anchor everything we do and shape a culture where purpose and performance go hand in hand.

Since our founding in Australia in 2004, Nucleus Network has successfully conducted over 1500 phase 1 clinical trials for biotechnology and pharmaceutical companies from the USA, Europe, Australia, Japan, South Korea, Taiwan, and China.

You’d be based at Hammersmith Medicines Research (HMR), our London site, but have oversight of oversees contract monitors.

We are seeking an experienced clinical trial monitoring professional to manage and support our clinical monitoring activities while contributing to the Quality Team.

Key responsibilities

  • managing and training a team of monitors in the UK and oversight of oversees contract monitors
  • site qualification, initiation, routine monitoring and closeout visits at HMR and other UK sites
  • preparing monitoring quotes, plans and reports
  • communication with the sponsor and investigator

· conducting audits on clinical trials, systems and service providers

Mandatory qualifications and competencies

Applicants must hold a degree or PhD in a life science and have a thorough understanding of clinical trials, substantial monitoring experience, a high level of accuracy and attention to detail and the ability to manage and develop a team. Strong communication, organisational, prioritisation and computer skills are essential.

Desired competencies

Excellent knowledge of the regulations governing clinical trials and auditing experience would be advantageous.

How to apply
Email your CV and a covering letter to careers@hmrlondon.com

Pay: £44,500.00-£50,000.00 per year

Work Location: In person

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