Medical Info Assoc II
Roche - South San Francisco, CA

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Demonstrates leadership among peers by consistent application and modeling of the appropriate compliance, behavior and conduct Is required to obtain and maintain full proficiency and knowledge of disease state, product and other aspects or issues as provided for and mandated by the company Stays abreast of internal and external developments, trends and dynamics, as these potentially implicate or evolve the development, launch and/or post-marketing medical direction of the assigned molecules/products, franchise(s), and/or overall therapeutic area(s). Includes maintaining a basic understanding of legal and regulatory topics relevant to healthcare/pharmaceutical/biotechnology industries Maintains a high standard and level of clinical knowledge in the specific therapeutic area(s) of assignment; reviewing and keeping updated on scientific/medical journals and other relevant publications Works with supervisor and other partners/stakeholders to evaluate development, launch and post-marketing strategies to determine medical communications needs and align MC Operations plans, projects, other tactics and resources Builds and maintains relationships with internal customers, partners and other stakeholders. Provides an in-depth MC Operations perspective, inputs and recommendations in the ongoing development and management of medical communications Acts as a MC Operations expert and resource to internal and external customers and consistently approaches interactions with clinical integrity and the highest professional ethics; consistently advocates for scientific accuracy and compliance Depending upon areas of assignment, may perform some or all of the following activities for assigned molecules/products: Ongoing literature surveillance across multiple sources Maintaining and managing current and accurate documentation and data in MC systems and databases Triaging internal and external requests for medical information regarding Genentech's products. Monitoring vendor inquiry documentation to ensure accuracy, legal, regulatory and general compliance with Genentech/Roche standards, policies, procedures and protocols Recording and tracking cases for unsolicited requests and/or other relevant operations and metrics Running regular and/or ad hoc reports from MC systems and databases Supporting MC scientists in writing and maintaining medical responses to internal/external requests for information and to address other inquiries Supporting MC scientists in their review of promotional materials, reprint dissemination materials, MSL (Medical Science Liaisons) slide decks, and other relevant content from internal partners for external audiences Identifying, communicating and addressing potential training issues, whether for internal MC Operations staff or external vendor partners As needed, provides additional medical communications/writing support to other internal customers, partners and stakeholders

QUALIFICATIONS & EXPERIENCE:
Bachelors Degree in life sciences or related disciplines and/or experience Knowledge of medical terminology, disease states, and treatments preferred Previous relevant industry work experience is a plus Must demonstrate a high level of proficiency with Microsoft Word, Excel and PowerPoint Previous experience navigating multiple databases/systems a plus Aptitude to learn and/or basic knowledge of marketed products and compounds in late development within assigned therapeutic area Has some understanding of, or aptitude to learn, pharma/biotech drug development processes (key functions involved and the path through development and into market) Basic knowledge and understanding of rules and regulations impacting medical communications practices Proven track record of meeting or exceeding objectives and goals Business travel, by air or car, is required for regular internal and external business meetings

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Roche is on a medicinal roll. The company operates two segments, pharmaceuticals and diagnostics, and sells its products in some 180...