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Head of Medical Affairs

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About the role

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HEAD OF MEDICAL AFFAIRS (FIRECREST)
DUBLIN or LIMERICK
 

Firecrest is a division of ICON, leading the way with innovation in the field of clinical trial site performance. Firecrest’s team of experts, technologists to clinicians, create customized technology solutions to meet the challenges of clinical trial management, enhancing the use of data, aiding our clients in bringing their products to market quicker and more effectively.

 

In support of the division's exceptional growth we are seeking a Head of Medical Affairs to provide medical, scientific and regulatory oversight across the  organisation. This is a key role with responsibility for managing a core scientific team and acting as the single medical point of contact for our clients.

 

The role has responsibility for leading and overseeing the strategic and tactical production of clinical trial products from a medical perspective.

Firecrest’s reputation is critically linked to the accuracy and applicability of our medical offering and its regulatory compliance across the development spectrum (early phase to phase IV). The Head of Medical Affairs will familiarise themselves with the relevant protocols, IDB and / or other client study material and provide oversight and input into all Firecrest projects / services offered, being available to impart medical, clinical and regulatory knowledge for each of our clients.
 
This is a brand new role and will require a forward thinking individual with client facing capabilities who will contribute actively as a strategist and consultant, providing Medical Affairs guidance in relation to our product portfolio. 
 
In addition to the above, the Head of Medical Affairs will represent Firecrest externally with key stakeholders, publishing papers and presenting at conferences and leading Investigator Meetings.
 
 DEMONSTRATE YOUR SKILLS!
 
We are seeking a 'Leader' with proven experience either from a CRO or    Pharmaceutical environment who has led multinational clinical trials and successful product approvals.
   
By the nature of your experience you will posess a medical degree, be able to evidence strong knowledge of current GCP, FDA and EU guidelines/directives and demonstrate experience of working at a senior level, leading cross functional teams.
 
 Alongside your medical expertise you will be required to show strong analytical capability and astute business acumen
 
The role will carry some travel (up to 30/40%) domestic or international.
 
What to expect:
 
ICON is a top five, global CRO with an innovative range of services and a competitive benefits package. Our employees are innovative, passionate and are rewarded accordingly for the significant part they play in our success.
 
Next Steps:
If your background is an appropriate match for the needs of this role and you are seeking the challenge that this position can offer, one of our Talent Acquisition Specialist will contact you for an initial discussion.
 
ICON is an equal opportunities employer and we offer a non discriminatory working environment.
 
*LI-VS1
            
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