i-Pharm Consulting

Director Clinical Information Development, Oncology

Location
Maryland
Salary
Negotiable
Posted
05 Dec 2018
Closes
19 Dec 2018
Ref
CMG9241
Contract Type
Permanent
Associate Director Clinical Information Development, Oncology | Oncology Clinical Information Director | Oncology | Immuno-Oncology

Location: Cambridge, United Kingdom OR Maryland, United States of America

Salary: Competitive + generous benefits package

i-Pharm Consulting have partnered with a multinational, top 5 global Pharmaceutical and biopharmaceutical company to help recruit for an Oncology Clinical Information Director.

Our client want to redefine the cancer-treatment paradigm. This will happen with their broad pipeline of next-generation medicines, which are focused principally on four disease areas – breast, ovarian, lung and haematological cancers, and they aim to bring six new cancer medicines to patients by 2020.

The role:

As the Clinical Information Science Director (CISD) within Oncology & Immuno-Oncology you will play a leading role in supporting global clinical directors and trial design teams in finding and structuring clinical information driving optimal designs for late stage oncology drug development. This position will sit within Information Practice unit who clinical information and knowledge for better informed decision-making and clinical development.

In the Biometrics & Information Sciences (B&I) team, you will be a part of the statistical and information experts for late stage (phase II and beyond) drug development. You’ll be part of a truly global team alongside some of the most respected statistical programming, information practice and analytics specialists in the industry.

Responsibilities

Clinical Trial Design -

As a strategic Director embedded within dynamic oncology drug project teams, you will lead the delivery of information clinical teams need to assist them in making decisions driving the late stage drug development process. Your knowledge of the clinical oncology landscape, of late stage clinical trial design process, and in utilising numerous information sources will enable you to collaboratively contribute with statisticians, medics and other experts in a cross functional team.

Requirements

* To be considered for this opportunity you will have demonstrable experience of late stage oncology drug development.
* Have a real passion for clinical data and information and proven insightful ability to know what information to seek, how to find it, and how to share it with the teams in a clear and meaningful way.
* You will be a creative thinker with an appetite for doing things differently.
* Deep understanding of the late stage clinical drug development process in oncology, immuno-oncology or immunology
* Deep understanding of the late stage clinical drug development process in oncology, immuno-oncology or immunology
* Have prior experience within Project Management from either a Medical Affairs, Clinical Trial or Regulatory Affairs scope.

This is a revolutionary opportunity to grow and develop your career to new soaring heights!

In order to be considered for new opportunity you must have proven experience within Oncology as you will be leading key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and decision makers.

If you feel your experience aligns correctly with the above requirements, please apply directly for additional information.

Associate Director Clinical Information Development, Oncology | Oncology Clinical Information Director | Oncology | Immuno-Oncology

Location: Cambridge, United Kingdom OR Maryland, United States of America

Salary: Competitive + generous benefits package

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