Skip to main content
Post your CV and find your next job on Indeed!

Clinical Trial jobs in Hammersmith

Sort by: -
    • Conducting audits on clinical trials, systems and service providers.
    • Excellent knowledge of the regulations governing clinical trials and auditing experience…
    • Support and potentially participate in aspects of clinical trial administration and coordination, gaining exposure to research activities.
    • A fair understanding of the drug development process and vaccine clinical trial design, statistics and findings.
    • In this role, you’ll play a vital part in the preparation and quality assurance of IMPs, ensuring the highest standards of safety and compliance.
    • Key requirements: * Experience in patient care - 2+ years minimum * Experience in clinical evaluation, clinical data assessment, and medical statistics -…
  • View similar jobs with this employer
    • Veterinary aspects of animal test certificates to conduct clinical field trials.
    • A good understanding of current animal health and topical veterinary issues and…
    • The role will be part-time, (approx. 20 hrs per week) that can be arranged flexibly around other commitments and will be based within our office on West Street,…
    • Experience writing clinical study protocols and clinical study reports directly.
    • Lead all scientific elements of clinical studies from protocol development…
    • Your work will help ensure that clinical trials are designed with patients, not just for patients.
    • Thorough understanding of drug development and every stage of…
    • Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements.
    • In-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management,…
    • Enthusiasm for innovation, including application of AI and advanced analytics to clinical trial oversight.
    • Typically, 8-10+ years of clinical research/clinical…
    • Lead Product Demonstrations & Clinical Evaluations - Deliver engaging product demonstrations, presentations and clinical trials, providing expert guidance and…
    • Familiarity with regulated environments (e.g. GxP, clinical, diagnostic workflows).
    • Starting from strategy and proposition definition to detailed operations and…
    • View all Deloitte jobs - London jobs - Delivery Manager jobs in London
    • Salary Search: Associate Director, Design and Delivery Lead, Life Sciences and Healthcare salaries in London
    • See popular questions & answers about Deloitte
    • The Ethics & Regulatory Compliance (E&RC) team help our clients to manage evolving risk areas, navigate regulations, behave ethically and grow responsibly.

People also searched:

clinical research
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

Let Employers Find YouUpload Your Resume