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    Clinical Trial Assistant - London, United Kingdom - RBW Consulting

    RBW Consulting
    RBW Consulting London, United Kingdom

    3 weeks ago

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    Description

    Role:
    Clinical Trial Assistant (CTA / Associate CPM)

    Location:
    Hybrid (4 days remote and 1 day per week in London)

    Company:
    Small Biopharmaceutical CompanySalary: £35,000 - £42,000 (depending one experience)

    RBW Consulting are excited to announce an exciting opportunity to join a unique small pharmaceutical client of ours.

    They are pioneering technology within vaccine storage and if they get the technology right , they will have massive growth potential.

    They are already collaborating with leading pharmaceutical companies within the vaccine space and their product is developing positively.

    They have a vacancy open for a Clinical Trial Assistant (CTA) to join their team and they can take someone on immediately.

    The CTA will have Associate CPM responsibilities and will be required to work independently with protocols and complete projects with little supervision.

    Therefore, someone with prior experience will be required for this position.

    This is a great opportunity to join a small company with a nice environment where you can gain exposure to different responsibilities and areas of the business.

    This will not only make for a more interesting day-to-day but will give you better career prospects as the company continue to develop.

    Responsibilities Collaborate with other company functional areas and the study vendors, oversee all aspects of the study activities and work to ensure the study timelines are being metAttend and participate in study meetings and communicate any study issues that may arise, as well as any items that may impact in the study budget and timelinesProvides input into clinical study protocols, clinical study reports, and other clinical documents as appropriate on assigned studies.

    Contribute to the development of the Master Informed consent for clinical studiesTo preparing, collecting, and tracking master study level documents (as appropriate); reviewing Regulatory and non-regulatory documents; tracking and management of vendor invoices and Purchase Orders (POs)Involved in internal process improvement activities such as SOPs or guidance documents, as assignedParticipate in the cross- functional TMF ReviewOther responsibilities that may ariseRequirements Life science degree or equivalentPrior CTA experiencePhase I and small biopharma experience preferredTo apply:

    Please click 'apply' or contact RBW Consulting for any further informationAbout RBW ConsultingRBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence.

    We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale.

    We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We've created a culture rooted in support, transparency and mutual commitment.

    We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

    We are an equal opportunities Recruitment Business and AgencyRBW Consulting is an equal opportunity workplace.

    We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset.

    We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status.

    We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

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