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Director Level Medical Lead

€Salary Negotiable | Belgium, Netherlands, USA |  Medical Affairs, Pharmaceutical Company |  Permanent  | Ref:889378

The Role

Director Level Medical Lead - Clinical Development - Vaccines - Global Pharmaceutical - Netherlands (Belgium and East Coast USA also considered) - €Salary Negotiable

 

The Company

World renowned Pharmaceutical Company with a Global footstep and reach to patients across a broad range of product areas including Devices, Diagnostics, Vaccines, Pharmaceuticals and Consumer Health.

 

The Role

You will be working within a subsidiary company of this Global Pharmaceutical company, a team who are dedicated to the development, manufacture and marketing of vaccines and antibodies to protect people worldwide from infectious diseases.Focussing on Paediatric vaccine development this role will include but not be limited to the following responsibilities:

  • Give input/feedback on the overall Clinical Development Plan in alignment with therapeutic area strategy

  • Initiate and moderate clinical meetings

  • Give input on Clinical Development Plan, Clinical Resource Plan, Overall Medication Plan, Overall Quality Monitoring Plan

  • Ensure projects and trials progress within the correct timeframe and to quality

  • Perform medical review and safety analysis of clinical trial subjects

  • Ensure timely interaction with the clinicians, advocacy groups and other experts

  • Member of the Medical Surveillance Team

  • Build and lead the clinical team

  • Interpret clinical safety and efficacy data

  • Support marketing activities - pre launch, publications, conferences

  • Key liaison with medical affairs, strategic marketing, regulatory agencies, external opinion leaders and advisory boards

 

You

You must be a Medical Doctor who has experience of Vaccine development and has worked at Director Level. This role reports into the VP Clinical Development

  • You will demonstrate leadership and management abilities

  • Significant experience in the design and conduct of vaccine trials or Phase I, II and III Clinical Trials

  • Experience in clinical documentation in regulatory dossiers

  • Paediatric experience preferred

 

What should you do next?

If you want to be part of an innovative, global team where your development is key to the organisation please apply below. Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there.

Consultant

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Jenny Downing

Which team do you work in?

Clinical Research, Medical Affairs and Regulatory Affairs 

Which area do you specialise in?

My focus is Senior Clinical Operations and Senior Medical Affairs

How do you keep up-to-date with the issues in your sector?

I try to keep up to speed with industry news sites and blogs but really the majority of helpful and interesting information comes through the conversations I have with my candidates and clients. 

What makes you #DistinctlyDifferent?

On a professional level - 12 years within recruitment specifically working within the pharmaceutical industry gives me the knowledge and overarching understanding of Clinical Research to really understand my clients and candidates' needs, regardless of functional area they sit within.

On a personal level - I have done a skydive in NZ, ridden an elephant in Laos, Scuba Dived in Vietnam, swam with sharks in Thailand (small ones!) and sailed a tall ship around the Caribbean (by sailed I mean I sat drinking cocktails while the crew sailed it). 

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