Medical Director - Global Clinical Development

London  ‐ Onsite
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Description

The contract will be 6 months in length (strong possibility of extending), it will be a full time role so it is essential that the potential candidates have availability for 5 days per week from January / February 2016. There will be flexible working - allowing 2 days from home per week.

The client would Ideally like a candidate that has Extensive Global Clinical Development and Medical Affairs experience in the specialty/ethical pharmaceutical industry.

Fully accredited Pharmaceutical Physician on the specialist register of the GMC.

In depth knowledge of UK, European and Global pharmaceutical business in relation to Due Diligence, Clinical Development Strategy, Medical Affairs, Market Access Publications, Marketing Support and KOL management.
Leads and drives strategy for the regional and/or global (US/EU/ASIA) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned pipeline compounds.

Apply clinical/medical decision making to clinical development issues. This individual interacts with and influences senior leadership decision-making for the projects by setting strategic direction. Success or failure directly translates to the ability of the company to meet its corporate goals for commercial products. The client would like the candidates to match the following requirements:

Specialties in Clinical Development, Medical marketing in addition to one or more of the following therapeutic areas: Gastroenterology, Nephrology, Haematology, Rheumatology, Dermatology, Cardiology, Surgical Oncology, Urology, General Surgery, Pharmaceutical Medicine.

REQUIREMENTS

*MD or internationally recognized equivalent plus moderate experience of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned).

*Relevant therapeutic experience (GI, Hepatology) with involvement in designing and/or conducting studies particularly in EU and Asia

*Previous experience successfully leading a clinical development team/matrix team with responsibility for studies in multiple regions.

*NDA/MAA/Submission experience preferred.

*Management experience

*Specialisation in endocrinology would be an important plus

SKILLS

*Superior communication, strategic, interpersonal and negotiating skills

*Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix teams

*Diplomacy and positive influencing abilities Knowledge

*Therapeutic area knowledge relevant to mechanism of action

*Regional/global Regulatory requirements

*GCP/ICH

Applicants must have UK / EU work permits / visa's in place before applying as this is a contract position there will not be a relocation package or sponsorship on offer.

To find out more about Real please visit www.realstaffing.com

Real Staffing, a trading division of SThree Partnership LLP | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales
Start date
02/2016
Duration
2016
From
Real Staffing
Published at
06.01.2016
Project ID:
1046717
Contract type
Freelance
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