Department: Medical Affairs

Job Title: Associate Director, Medical Information

Job Location: Seattle, WA

Requisition #: 2009A9JS

Description:
This position provides leadership, direction, and compliance expertise to the Medical Affairs Department. The individual in this position is responsible for the provision of accurate, evidenced-based data and information related to the CTI product portfolio to internal and external customers. The individual in this position must maintain SOPs, direct the department in setting and obtaining goals consistent with corporate goals and objectives, oversee systems and processes that comply with guidelines directing dissemination of scientific information in the current regulatory and legal environment and support team members in professional growth. In addition, the position requires the ability to manage outside vendors engaged in supporting CTI business, as well as budget management and leadership within the Medical Affairs team. Responsibilities will include interfacing with Clinical, Medical Communications, and Pharmacoviglence to ensure consistent and accurate communication about product MOA, side effect profiles, clinical data, etc. Direct oversight of call center and the manner in which verbal and written medical information is provided to internal and external customers. Identify opportunities, and liaise with appropriate CTI team members, to continually provide appropriate and up-to-date medical information. Work closely with CTI team members (MSLs, Sales and Marketing, Corporate Communications, etc) to respond to requests for data and information from HCP at major scientific congresses such as ASH and ASCO.

Job Requirements:
Requires a Bachelor’s degree in a medical field or equivalent with preference for an individual with an advanced degree in a medical field (Master’s, PharmD, PhD or MD) and 8+ years of experience (5+ with an advanced degree) in a biotech or pharmaceutical company focused on medical information. Must have proven medical writing skills (samples should be provided), a strong background in oncology and experience in interfacing with HCP. Prior supervisory experience is desired. Knowledge of cancer treatment from medical, pharmacy and nursing perspectives is required, as is basic familiarity with the regulatory and business aspects of phase I-IV clinical trials. Ability to interact with others in a confident, professional but flexible manner is required. Ability to work on cross-functional teams is essential. Excellent writing and literature research skills are required. Absolute attention to detail is necessary, as is the ability to prioritize and execute high-quality work under time pressure while remaining professional and productive. Knowledge of FDA, OIG, and Pharma guidelines overseeing the dissemination of medical information to HCP and patients is expected. The position will be based in CTI’s Seattle headquarters and will require some travel to major scientific meetings and educational conferences.

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