Clinical Trial Coordinator - Greater London - myota

    myota
    myota Greater London

    6 days ago

    Description

    About the role

    We are looking for a motivated and organised Clinical Trial Coordinator (full-time, 12-month fixed-term) to support the delivery of clinical trials at myota. This role is ideal for someone with prior experience in human research studies who is ready to take on increased responsibility in a dynamic, mission-driven startup. You will play a central role in the day-to-day coordination of our clinical trials, helping to ensure all activities run smoothly and to the highest ethical and regulatory standards. The role offers hands-on experience across multiple aspects of clinical trial delivery.

    You will required to be on-site at our London office full-time to delivery clinical trial activities.

    Key responsibilities

    • Project coordination: Support the planning and operational delivery of clinical trials, from ethics submission to final data collection
    • Regulatory & ethics: Prepare and maintain documentation for ethics committees and other relevant bodies
    • SOPs & documentation: Maintain study documentation and trial master files in compliance with regulatory standards
    • Site & vendor communication: Liaise with study sites, labs, couriers, and external vendors to support smooth trial operations
    • Participant recruitment & retention: Help coordinate recruitment activities and track participant enrolment and communication
    • Data collection & quality control: Support data entry, monitoring, and verification, ensuring accuracy and completeness
    • Logistics: Manage supplies, sample kits, and shipment schedules, including packaging and coordinating deliveries where required
    • Reporting: Assist with progress updates, summaries, and internal reporting for the project team

    What we're looking for

    • BSc or above [MSc desirable] degree in life sciences, health sciences, nutrition, or a related field
    • Experience coordinating or supporting clinical trials or human research studies (e.g., in NHS, academic, or commercial settings)
    • Working knowledge of Good Clinical Practice (GCP) and research governance
    • Excellent organisational and time management skills
    • Strong attention to detail and ability to follow SOPs and protocols
    • Good written and verbal communication skills
    • Familiarity with data entry systems or EDC platforms

    Experience working in a startup or small team environment

    • GCP certification
    • Familiarity with ethics submissions (e.g., IRAS, REC, HRA)

    What you'll get

    • Autonomy and real responsibility from Day 1: You'll be owning and driving key projects from the very start, making a direct impact on our growth and giving you the chance to learn and develop lots of new skills.
    • Work directly with the founding team: You'll collaborate closely with our experienced founders, gaining invaluable insights into the workings of a fast-growing start-up and the wider business landscape.
    • Career development: You'll be part of a rapidly expanding company with endless opportunities for personal and professional growth.
    • Become a gut health pro: Work alongside leading PhD scientists, deepening your knowledge of the microbiome and becoming an expert in gut health.
    • Dynamic & creative work environment: Join a small, innovative team that values creativity and new ideas, and where your contributions will truly make a difference.
    • Central London location: Work from our office (and with part-time office dog Winston) in the heart of a vibrant start-up community.
    • Top-notch equipment: All the tools you need to succeed, including a laptop, monitor, and any other equipment required.
    • Free myota subscription: Stay healthy with a complimentary subscription to our innovative gut health products.

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