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Job Details

Associate Medical Director for a Global Neurology Role - North Carolina (full and extensive re-location package available)

Company: Advanced S&S (USA)
Location: North Carolina
Reference: TMADV / 201018B
Closing Date: 19 Dec 18
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

We have a new opportunity for an Associate Medical Director to join an expanding Biopharmaceutical company in a role with Global project responsibility that will cover an expansive and highly exciting and varied Neurosciences portfolio. If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig on 855 505 1382.

Requirements:

We have a new opportunity for an Associate Medical Director to join an expanding Biopharmaceutical company in a role with Global project responsibility that will cover an expansive and highly exciting and varied Neurosciences portfolio.

Location: RTP, North Carolina

This organisation is a special one, and is very different to other top 50 organizations. They are not departmentalized, or rigid in approach or have grown through buying a number of other companies each year – this organization has grown and developed by having a dynamic, innovative and entrepreneurial approach to drug development and product registrations specifically within their Neurology franchise.

The Role… within the Neurology franchise you will be accountable for providing medical expertise and medical leadership into clinical development strategies to allow project teams to successfully deliver the clinical studies aligned with the Target Patient Value Profile (TPVP) and Clinical Development Plan (CDP). The focus will be on all aspects of clinical drug development including but not limited to medical input into indication selection, assessment of current and future treatment strategies, unmet need, target patient population, TPVP, clinical development plans, clinical study protocols and reports and regulatory submission documents.

Scope….You will be accountable for providing medical expertise and medical leadership into clinical development strategies to allow project teams to successfully deliver the clinical studies aligned with the Target Patient Value Profile (TPVP) and Clinical Development Plan (CDP). The focus will be on all aspects of clinical drug development including but not limited to medical input into indication selection, assessment of current and future treatment strategies, unmet need, target patient population, TPVP, clinical development plans, clinical study protocols and reports, regulatory submission documents. 

Education and Experience….It’s essential that you have a Medical qualification (MD) and experience in Neurology with a good knowledge of clinical development, including regulatory framework and the ability to communicate effectively with internal (including senior and executive management) and external key stakeholders (including regulatory authorities), operating as a strong team player and high performer within global matrix teams.

Package… this role come with a strong and lucrative basic salary, bonus of approx. 20% each year, stock options & LTI’s worth an additional $30,000 a year, and a blue chip benefits package including, health, dental, pension, death in service, life insurance with good options to work up to 3 days a week from home.

To Apply…. If you wish to apply for this role, please send your CV to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or global career options in Clinical, Medical or Regulatory Affairs, call Theo Moore or Matt Greig on 855 505 1382

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About Advanced

Advanced Regulatory is a division of Advanced Search and Selection Ltd and has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas - we have offices both in the UK and in Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at www.advregulatory.com.

We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.

Keywords / Key words: Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs.

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)207 801 3380
Website:  Visit Our Web Site

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