Vice President, Clinical Development, Rare Disease - Europe or US

  • Full-time
  • Department: Executive c

Company Description

Ergomed is a rapidly growing  global clinical research company.  We perform clinical trials  for rare and complex diseases.

Ergomed Plc is a public company on the London stock exchange.

The company boasted 40% growth in its revenues in its last report.  This success is due to the hard work of our highly skilled employees and our subsequent  reputation for excellence with our clients. 

Job Description

As a key leader, you will interact with executive leadership, customers, business development, and project teams to drive the strategy for Rare Disease projects globally.  Provide leadership and oversight to the development of global strategies, provide scientific and therapeutic consultation, and oversee the execution of the global therapeutic strategy.  Provide direction for the growth of the Rare Disease portfolio and provide consulting, as needed. You will be expected to actively participate in company initiatives and development. You will lead broadly in a cross-functional and multi-cultural environment and leverage their extensive experience to represent regulatory.

JOB RESPONSIBILITIES

  • Drives overall strategy and direction for Rare Disease globally.
  • Acts as a primary senior-level contact for customers.
  • Participates in customer proposals, Request for Information (RFIs), presentations, proposal defenses and Steering Committees.
  • Provides scientific/regulatory oversight and project/therapeutic training to project teams.
  • Responsible for coordinating the acquisition of necessary medical/scientific input from outside experts/consultants/advisors.
  • Represents the Company by attending industry meetings, speaking engagements, participating in booth exhibitions, etc., and by publishing scientific or industry related articles in industry journals.
  • Participates in the development of Standard Operating Procedures (SOPs), medical/scientific tools, training, staffing requirements, etc.
  • Interacts with senior management and contributes scientific/medical input to other departments, as appropriate.
  • Ensures quality standards are set and maintained over all areas of responsibility

Qualifications

Experience Required:

  • Expertise and extensive clinical research experience in Rare Disease area (with related degree and academic qualification).
  • Detailed knowledge of Rare Disease strategy.
  • Previous experience in a CRO environment.
  • In-depth knowledge of Regulatory Authority regulations and strong understanding and usage of medical terminology.
  • Strong business acumen and proven ability to navigate in a complex matrixed global environment.
  • Ability to handle multiple tasks to meet deadlines in a dynamic environment.
  • Effective organizational, presentation, documentation and interpersonal skills.
  • Strong leadership and communication, verbal and presentation skills.
  • Solutions provider; converts challenges to opportunities.
  • Ability to navigate the management matrix; strong people and negotiation skills.

Additional Information

All your information will be kept confidential according to EEO guidelines.

We're an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

 

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