Medical Director

  • Salary:
  • Location:
  • Job Type:
  • Date Posted:
  • Competitive
  • Netherlands
  • Permanent
  • Now Expired

THIS JOB HAS NOW EXPIRED.

As a qualified cardiologist you will play a central role in our clinical development team: defining and pursuing market opportunities, consult internally on proposals and support the trial management in planning and conducting clinical trials in the cardiology areas.

Your duties include:

- Participate in the definition of therapeutic targets that are characterized by unmet medical needs and emerging promising therapies
- Support designation of high priority molecular entities for prospective engagement with sponsors
- Support operations and marketing strategies to enhance company's visibility and position including publications, presentations at society and hosted meetings
- Coordinate with Sales and Operations the development of new, and enhance existing, client relationships
- Developing coherent, robust and well-articulated written responses to business opportunities
- Help to develop costing models for specific proposals
- Present medical/scientific analysis and plans at bid defense meetings
- Help develop plans and provide guidance for site targeting, feasibility and selection
- Provide strategic medical and scientific input in operational development and trial management
- Assist in projecting operational risk and plan for mitigating this risk
- Provide Operational Team and investigator/site training at investigator meetings
- Develop, review and revise protocols, case report forms, medical responsibility plans, adverse event reporting plans, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications
- Review aggregate laboratory values, adverse events, coding and data tables, listings, and figures in the assessment of safety and operational efficacy
- Provide on-call coverage for protocol and safety issue after-hours on a rotational basis
- Perform other duties as assigned

Travel:
- up to 30% of time

Education/Qualifications Typically required education:

- MD degree
- Formal training in Internal Medicine and Cardiovascular Disease with a fellowship in the latter
- Preferred: experience in electrophysiology with additional fellowship training
- Fluency in written and oral business English

Experience Typically required experience:

- Minimum of 2 years experience in academic medicine or clinical medicine practice with involvement in clinical trials
- Preferred: industry experience of at least 2 years in clinical trial management
- Ability to work in a collegial, matrixed environment
- Ability to write clear, insightful medical reviews and protocol analyses
- Excellent presentation skills
- Ability to work independently and in teams
- Good prioritization and organization skills
- Ability to adjust to changes in tasks as required

EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

Covance

Covance is one of the world’s largest and most comprehensive drug development services companies with more than 11,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medic...

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