i-Pharm Consulting

Clinical Information Director

08 Jan 2019
22 Jan 2019
DM 32
Regulatory Affairs
Contract Type
The Company

Our Client, a global bio pharmaceutical organisation with 3 R&D sits and 31 production facilities across 18 countries, is seeking a Clinical Information Director to join their team on a permanent basis.

The Position

As the new Clinical Information Director, you will be heavily involved in late stage Oncology drug development. You will sit within the organisations Information Practice unit and be responsible for the (re)use of clinical information and market knowledge for better informed decision making and clinical development. You will also lead key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and decision makers.

As part of the remit, you will also:

* Influence late stage drug development decisions by using data to support clinical trial design.
* Lead the design team by collaborating with project stakeholders to plan and schedule project timelines tracking project landmarks
* facilitate access to complex information for the drug project and ensure access to and (re)use of clinical information, documents and data.

The Person

The ideal candidate will be degree qualified with demonstrable experience of late stage oncology drug development. You will need to possess good understanding of project management techniques and methods plus, experience in clinical information or science information setting in the application of information and knowledge management.

To be considered for this exciting opportunity, you will also need:

* Good organizational skills and the ability to multitask
* Demonstrated leadership capability
* Great attention to detail


Competitive salary and company benefits apply

To discover more about this opportunity, apply now or contact David Maguire on 020 3873 7067 or email Dmaguire@I-Pharmconsulting.com for a confidential discussion.

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