Dear Colleague,
  Fantastic opportunities at i3 Innovus
  Opportunities at i3 Innovus
i3 Innovus is a world leader in health economics, outcomes, and late phase research. We uniquely couple expert study design consultation with rich datasets to enhance the success of late phase studies, helping you achieve both your scientific and commercial objectives while maintaining regulatory compliance.
Senior Project Manager � Late Phase (219835)

This role will lead and manage the efforts of all key functional departments to perform all project-related activities according to project milestones/timelines to conform to the study processes.
As the primary liaison between the Customer and i3 Innovus you will oversee the project team communication to ensure a complete understanding of expectations and scope of work.  Essential to this role will be to manage the project budget and specifications, maintain communication with business development to discuss the cultivation of any identified business opportunities.

Late Phase Project Research Associate (LPRA) (214972)

As a LPRA you will be involved in all aspects of research activities which will include providing support in the planning, execution and control of studies within our service mix with specific concentration on handling the Ethics Committee and regulatory process and managing and supporting participating sites to ensure study success.
We are seeking accomplished, results focused individuals who enjoy working in an international team and whose drive and enthusiasm will compliment our dynamic, client focused group around Europe.   

Site Management Centre Manager � Late Phase (219842)

This role will be responsible for leading the In-house CRA function and will have line-management responsibilities for Late Phase Research Associates.

Duties will include overseeing all aspects of late phase research projects from inception to completion, which will: site management activities, recruitment of study investigators, regulatory document and site contract collection, Institutional Review Board (IRB)/Ethic Committees (EC) submissions, and preparation of study manuals, operational plans, and project specific templates/correspondences.
If you are interested in finding out more about how you can develop your specialist knowledge within a market leading global Clinical Research Organisation, please call Anna Shaw on +44 1628 408457 or e-mail
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