Clinical Trials Manager

Choosing the right company when looking for your next role can be a challenge. We partner with a select few Medical affairs agencies, Clinical Research organisations and Healthcare Technology Organisations to match candidates with the correct company, perfectly matching your values, goals and work like balance needs with our partners.

We partner with organisations that have people at its centre, share our passion for collaboration and ongoing training and development programmes.

So whether you're looking to work within an office, remote or have niche requirements we'll help you select the right agency to allow you to thrive in and out of work.

You'll thrive if you:

• Act as primary point of sponsor contact for Study sites and CROs. Escalate issues as needed to appropriate stakeholders.
• Lead combined study team(s) ensuring effective cross-functional teamwork among team members including both internal and external stakeholders. Depending on size and scope of trial(s), this duty may be performed in collaboration with the Head of Clinical Operations and/or Program Director.
• Per SOPs, plan, implement and monitor progress against those project plans and revise/update as necessary throughout the lifetime of the study. Create and manage timelines & budget variance to required project plans.
• Understand the trial delivery strategy, costing assumptions and resulting budget for assigned trial(s) in order to manage vendors. Tracking and reporting on clinical trial progress against timelines and budget. Monitor trial assumptions, schedule and costs to ensure all remain on track with the contract(s).

What our partner's like to see:

• A life science degree or nursing or similar qualification.
• Clinical Trial document writing including protocol writing
• Site monitoring
• Experience of site feasibility and study start up activities
• Medical imaging and/or oncology therapy experience
• International clinical trial management experience in the pharmaceutical and/or CRO industry.
• Radiopharmaceutical and Oncology experience highly desirable.
• Expert knowledge of ICH GCP and FDA Guidelines. Knowledge of international regulatory requirements for the conduct of clinical development programs is also a bonus.
• Working knowledge of project management processes.
• Experience managing trials in a virtual environment.
• Ability to work collaboratively on multi-disciplinary project teams and proactively manage relationships with external vendors
• Skilled in organization and prioritization with a strong attention to detail
• Demonstrated ability to handle multiple competing priorities, utilize resources effectively and adapt flexibly to changing priorities.
• Must be able to communicate effectively in the English language
• Ability to work independently as well as part of a team.
• Effective computer skills with good working knowledge of a range of computer programs.

Apply now and let's have a conversation all about you, so we can find your perfect next role.

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