Michael Page Life Sciences is looking for a Senior Associate Study Manager to work for our pharmaceutical client based in Cambridge. Role description Based in Cambridge the overall purpose will be to coordinate study-level investigational product arrangements whilst also supporting the clinical trials team. The Senior Associate Study Manager will largely be responsible for overseeing and contributing to the preparation of the clinical protocols, consent forms and monitoring plans. You will also be responsible for the following: • Identifying clinical trial investigators • Assisting with study start up, managing the review of consent forms, tracking budgets • Providing extensive support for the CRA's and other clinical team members across the clinical site • Work regularly with all team members, communicating effectively to the team any clinical updates and timelines/budgets • Supporting vendor activities including training and development of vendor specifications • Continue to grow your own clinical knowledge whilst training and assisting those around you To be considered for the Senior Associate Study Manager you will need to display the following competencies: • Qualification of BA/BS/BSc • Experienced in a medically related field • Experience of working in a biotech, pharmaceutical or CRO company • Must have a good level of understanding of the drug development process • Experienced in budget management, leading a team and building external relationships Michael Page is working with a leading pharmaceutical organisation based in Cambridge What's on offer A fantastic financial package.