Medical Director Oncology
6 giorni fa
At ICON, it's our people that set us apart.
Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation:
Accountability & Delivery, Collaboration, Partnership and Integrity.
We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point.
In short, to be the partner of choice in drug development.
That's our vision.
We're driven by it.
And we need talented people who share it.
If you're as driven as we are, join us.
You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
We are currently looking for a Medical Director - Oncology for our Medical Affairs Department in Mannheim or Berlin/Germany, Reading/UK, Sofia/Bulgaria, Milan/Italy or Madrid/Spain.
Joining our Medical Affairs Department working in a fast-paced, client-focused global environment the Medical Director's specialist expertise is called upon throughout the entire lifecycle of a project and as such the Medical Director plays a pivotal role in our business and project teams.
Alongside Business Development the Medical Director is a key contributor in raising our business profileto ensure we are the preferred partner for our clients with support on their projects.
As well as sharing your vast medical expertise at investigator meetings, kick-off meetings, and client face-to-face meetings other responsibilities will include:
Maintaining a strong consultative relationship with the client throughout the project lifecycle
Providing input into the creation of the protocol and other study-related documents
Participating in discussions with regulators, key opinion leaders, senior management and our clients
Delivering training to external project teams and colleagues
Reviewing medical data on the indication, inclusion / exclusion criteria and other medical issues to ensure our overall project deliverables are achieved and patient safety priortitised
Collaborating with our Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plans
You are:
An expert in your field with an affinity to lead and inspire.
We want our employees to succeed and ensure that they are set up for this success through constant training, development and support.
To enable success in this position you will have the following:
A medical qualification with license to practise and board certification
Experience in the desired therapy area is essential, ideally with experience in phase II-III projects either in industry or as an Investigator
Experience writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal is preferable
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