(US-Texas) Our client is a leader in the development of cardiac implantable devices, including prosthetic heart valves, and medical technology areas of business. They are in search of a Director of Marketing who will be responsible for the overall management of the department. RESPONSIBILITIES: ·Hire, train, mentor, supervise, and evaluate the marketing personnel ·Market evaluation of competitive activity, pricing, and distribution activities ·Develop and execute US marketing plans ·Marketing and business plan process deployment ·Introduction of new product lines ·Policy development for new products and plans to increase market penetration ·Management representation of product teams and support field sales personnel ·Plan and develop marketing programs to achieve market share, sales and profitability targets ·Evaluation of market reactions to advertising programs and product packaging ·Develop and manage marketing budget ·Manage market research activities, clinical marketing, communications and public relations ·Implementation of quality systems ·Report all unsafe activities to supervisors and/or safety managers EDUCATION: ·MBA preferred, Bachelor's degree required (Marketing) EXPERIENCE: ·10+ years in the marketing of medical implantable products or equivalent ·Domestic and International experience preferred Competitive salary + bonus + relocation assistance.
(US-California-San Francisco) Currently, our client is looking to fill the role of clinical specialist in the San Francisco area. This individual would need to be an RN, with preferred experience in the area of ob/gyn. A background of employment with a medical device company would be ideal, but other individuals would be considered. The responsibilities include up to 80% travel, visiting physicians and surgeons, and educating them on using the device. Looking to fill this position as soon as possible. Please send resumes along with a cover letter summarizing your relevant background.
(US-California) The ideal candidate will fulfill the role of Biostatistician on multi-protocol projects. S/he will develop protocols, review CRFs, and prepares analysis plans. In this role, the Statistician will also communicate with clients regarding statistical analysis issues as they arise. S/he will be responsible for interpreting analyses and writing statistical sections of study reports. S/he may also serve as Project Manager on various small Statistical Operations projects. QUALIFICATIONS The ideal candidate for this position will have either a Ph.D. in Statistics or Biostatistics complemented by one year of industry-affiliated working biostatistical experience in the clinical trials environment or a M.S. degree in Statistics or Biostatistics complimented by three years working biostatistical experience in the clinical trials environment. S/he will have knowledge of complex statistical methods that apply to Phase I-IV clinical trials complimented by strong working knowledge of SAS, familiarity with other packages (S+, SUDAAN, StatXact) COMPENSATION Compensation is competitive with a base compensation range between $65K-$85K and includes a comprehensive benefits package. Relocation is available for this position.
