Job Title

Principal Medical Scientific Expert, CVM

Salary

£76,000 - £100,000

Job Type

Clinical Project/Program Management, Clinical Sciences/Genetics/Genomics, Project Control & Budgets, Medical/Scientific Information, Medical Non GMC Roles

Location

Switzerland

Employment Type

Permanent Job

Employer Type

PM Pharmaceutical R&D HQ (Global Or EU)

Seniority

Department Manager/Associate Director

Duration

 

FTE Hours

Full Time 35 - 40hrs Per Wk

Vacancy Status

Open For Applications

Date Posted

Wed 8th Oct 2008, 11:49am

Our Client, a top 5 Pharma company, seeks a permanent Principal Medical Scientific Expert, who will be responsible for providing medical/scientific input and expertise to the global cardiovascular and metabolism group.

Major Accountabilities: Provide medical scientific input to all activities related to planning, execution and reporting of clinical trials, development of trial related documents, development of presentation material for trial-related advisory boards, investigators meetings, protocol training meetings, ongoing review of clinical trial data, final analysis and interpretation; Serve as disease area scientific and medical expert for internal and external customers; Provide support for medical marketing activities (e.g., KOL management, advisory boards, launch support, promotional material); Provide medical expertise to the development of Confirmatory and Life cycle management Clinical Development Plan, including the development of local clinical programs, developmentof Health Authorities' submissions including authoring clinical components of dossier, preparing presentations, and leading submission follow-up activities.

Qualifications: Medical degree with unique knowledge for successful clinical program development and execution required; Fluent English (oral and written); Advanced medical/scientific writing and communication skills; Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area; Proven ability^to work both independently or in a cross functional team setting, including a matrix environment; Demonstrated ability to establish strong scientific partnership with key investigators in assigned TA; Medical expertise within the cardiovascular therapy area is required.