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452 jobs match your search criteria:
| Date | Job Title | Job Level | Location | |
|---|---|---|---|---|
| May 28, 2013 |
Medical Communication Scientist
Medical Communications Scientist is able tocommunicate relevant, timely, accurate, and balanced clinical information onGenentech's products, positively influencing their safe and effective use.
DESCRIPTION: The Medical Communications Scientist is able tocommunicate relevant, timely, accurate, and balanced clinical information onGenentech's products, positively influencing their safe and effective use. Ableto evaluate medical literature as well as write, review, edit, and approvemedical content to ensure appropriate clinical context and accuracy. Providesmedical responses through various communication channels (response documents,web-based media, scientific meetings, etc.). Is also able to provide trainingrelevant to Genentech's product portfolio. Has a basic understanding oflegal/regulatory topics adequate to describe the basis of Medical Affairspolicies and procedures, and applies this knowledge to the review ofpromotional materials and Medical Affairs documents. The Medical Communications Scientist is able to assist in the development andimplementation of Medical Communication policies and procedures, establish andsupervise the work flow for delegated projects, and assess incoming requestinformation to determine required action and triage based on internal policiesand procedures. Can convey and acquire medical information as well ascommunicate and work effectively with members of the Medical Communicationsstaff and customers which include but are not limited to: Sales, Marketing,Managed Care, Clinical Development, Product Safety, Regulatory, Legal, andCorporate Partners. ... |
Experienced | South San Francisco, California | |
| May 9, 2013 |
Senior Financial Analyst, Commercial Finance Operations
Purpose: Responsibilities: |
Experienced | South San Francisco, California | |
| Jun 6, 2013 |
Associate Director, Medical Communications
Purpose In partnership with senior leadership, responsible for strategic direction and execution of medical communication plans for marketed products, pipeline molecules, and therapeutic area support. Oversight for MC scientist teams. Ensures product specialist resources are positioned to support current and future company needs. Accountable for the long-range financial planning and resource management for med comm product support. Liaison responsible for directing and influencing corporate groups to achieve shared goals and objectives. Job Description:
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Manager with Direct Reports | South San Francisco, California | |
| May 3, 2013 |
Study Data Manager (CDC II)
Clinical Data Management (CDM) is a department within the Biometrics function of the Product Development (PD) organization. CDM provides data management expertise to study management teams in PD and in gRED (Genentech Research & Early Development).
RESPONSIBILITIES:
The Study Data Manager (SDM) is a core member of Study Management Teams and serves as the study data management contact at the study and/or program level, providing expert guidance to program teams. The Study Data Manager leads the CDM study team and maintains oversight of all study start-up, study conduct and study close-out data management issues, activities and deliverables for one or more studies. The SDM interacts regularly with Clinical Data Management groups to ensure that project objectives are understood and met and provides technical coaching and mentoring on data management activities to colleagues. The SDM also performs the following: provides early strategic input into protocol design focused on data management issues; leads the development of eCRFs and database development and testing specifications by interacting with other functional area representatives; responsible for the oversight of all data review and cleaning activities involving close interaction with project clinical research professionals; responsible for the implementation of standards within Study Data Management across one or more CDM study teams; develops and executes ad hoc database queries utilizing data review and query tools; manages projects resourced externally via contract research organizations or corporate partners; provides support to ensure that study conventions, processes, knowledge sharing and best practices exist across all studies within a program; participates in departmental discussion groups, formal working groups or special projects. ... |
Experienced | South San Francisco, California | |
| May 6, 2013 |
Scientist - Development Toxicology
The Department of Safety Assessment at Genentech provides scientific leadership and plays an active role in the process of drug development from the discovery period through marketed products.
We are seeking a Scientist in the Department of Safety Assessment to support drug development. This role will involve working in a collaborative team environment as part of the comprehensive safety assessment of Genentech therapeutics by providing toxicology representation to biotherapeutics programs.
Responsibilities: Successful Scientist candidates will provide scientific leadership and play an active role in the process of drug development from late-stage discovery through marketed products. Working in a collaborative team environment, the Scientist/toxicologist leads the safety assessment of Genentech therapeutics by creating a best-evidence synthesis of existing knowledge and comprehensive investigations of toxicologic activity. The successful candidate will design and supervise toxicology studies to support the goals of biotherapeutics project teams, work closely with Study Monitors, Pathologists and Pharmacokineticists to deliver high quality GLP and non-GLP in vivo study reports and, as needed, represent Genentech in meetings with regulatory authorities. Responsibilities include interdisciplinary project team membership, preparation and review of regulatory documentation, study reports and manuscripts, participation in toxicology and pharmacology initiatives, and other active cross-functional collaborations. Additional responsibilities include investigations into mechanisms of toxicity, proactive management of potential safety liabilities and communication of impact to teams and governance committees. Experience with cross-functional teams and capability to build productive cross-functional collaborations both within and external to Genentech are desired. In addition to activities listed, Senior Scientist candidates will provide independent leadership in the design and implementation of safety assessment strategies for Genentech’s project portfolios and lead or provide support to interdepartmental and cross-industry initiatives. May provide supervision, mentoring, and career development to toxicologists. ... |
Experienced | South San Francisco, California | |
| Jun 5, 2013 |
Associate Scientist- Toxicology (Risk Assessment)
Responsibilities:
The Safety Assessment Division of Genentech is seeking a toxicologist with 0-3 years experience in general toxicology and an interest in human health risk assessment. This position will report to the Director, Product Quality and Occupational Toxicology. The Associate Scientist will conduct analyses of available data and generate documentation to provide guidance for decision making to product quality, product process, drug development, and environmental health and safety (EH&S) teams. Examples of specific duties include conducting health-based risk assessments for active pharmaceutical ingredients (small and large molecule), process-related impurities, process residues, extractables and leachables, and small molecule intermediates. Additional duties involve the evaluation, interpretation and communication of available scientific information for active pharmaceutical ingredients and incorporation of these data into documentation in compliance with hazard communication requirements, the development of occupational exposure limits (OELs), and MSDS maintenance for Genentech's products in collaboration with EH&S. This is an excellent opportunity to gain early entry to an industry position with a company that develops novel proteins and small molecules for the treatment of unmet medical needs. ... |
Experienced | South San Francisco, California | |
| May 6, 2013 |
Key Service Area Manager - IxRS
Division/Function: GPPS-EACM / Service Provider Mgt Position Purpose: Develops and delivers high value sourcing models and outsourcing strategies on the IxRS service category to support the out-sourcing needs of PD, pRED, gRED, GPS and GMA/gMED Main Responsibilities and Accountabilities: In general * To develop and refine a strategic sourcing plan for the category including determination, implementation and management of the applicable governance structure * To liaison with Roche stakeholders (PD, pRED, gRED, GPS and GMA/gMED) to ensure that the Biometrics sourcing strategy is aligned with in-house capabilities, with current and future needs and capacity * To provide advice and guidance to GPPS Contracts & Outsourcing Business Managers in the development and management of key service area domain contracts as well as to provide advice and guidance to project and/or study teams on this category * To manage all individual service provider relationships within the category, including contractual (MSAs), vendor performance and issue resolution * To lead performance management with service providers and to facilitate/expedite issue resolution Specific to IxRS Key Service Area: * To maintain an oversight of the IxRS category including ongoing management of spend and demand (including identification of efficiency and value adding opportunities). This category includes over time oversight of spent for also ePRO/PRO * To act as IxRS subject matter expert; contribute or lead relevant IxRS initiatives (i.e. cross functional working groups), maintain awareness of IxRS services, developments and providers globally ... |
Experienced | South San Francisco, California | |
| May 1, 2013 |
Data Acquisition Specialist/Sr Data Acquisition Specialist
The DAS is responsible for the specifications, acquisition, loading and delivery of non-CRF data including IxRS, laboratory, pK and other data. Responsible for the production of non-CRF data collection specification documentation Defines the study specific non-CRF data handling strategy Collaborates with SMT to agree on vendor expectations for the collection and transfer of data Reviews and refines the technical requirements with service provider to establish the transfer of non-CRF data Responsible for establishing appropriate transfer methodology with external data provider Provides transfer methodology training and documentation on non-CRF data for external vendors. Responsible for configuring the data loading tools based on data collection specifications Receives, uploads, confirms and communicates status of test data transfers to validate and accept file format and database structure Performs verification and resolves data transmission, file format and loading errors with data providers Proactively checks all inbound non-CRF electronic data for any potentially unblinding data as defined in the protocol and ensures study integrity by sequestering unblinding data until data release is authorised Delivers data to external recipients and review bodies via established transfer methodologies Represent CDM on IxRS sub teams and works with the Study Management Team to develop IxRS specifications and implement the system Coordinates and plans subfunction activities to meet program-level deliverables and timelines Develops and maintains the subfunction standards for the studies in a program Collaborates with Data Modeling Specialists to define study data collection standards for new assessments and collaborates with them to implement new standards Effectively communicates ideas, project goals and status of work and can present to senior management Proactively develops solutions to complex problems requiring the regular use of ingenuity and innovation Sets targeted timeframes for deliverables and anticipates potential scenarios that may result in timeline delays; able to influence and negotiate a positive outcome Proactively develops contingency plans to reduce impact of risks that may occur, to analyze effectiveness of strategies and to monitor and review risks |
Experienced | South San Francisco, California | |
| May 22, 2013 |
Scientist, Small Molecule, Development Tox
The Department of Safety Assessment at Genentech provides scientific leadership and plays an active role in the process of drug development from the discovery period through marketed products.
We are seeking a Scientist in the Department of Safety Assessment to support drug development. This role will involve working in a collaborative team environment as part of the comprehensive safety assessment of Genentech therapeutics by providing toxicology representation to small molecule programs.
Responsibilities: The successful candidate for Scientist will provide scientific leadership and play an active role in the process of drug development from late-stage discovery through marketed products. Working in a collaborative team environment, the Scientist/toxicologist leads the safety assessment of Genentech therapeutics by creating a best-evidence synthesis of existing knowledge and comprehensive investigations of toxicologic activity. The successful candidate will design and supervise toxicology studies to support the goals of small molecule project teams, work closely with Study Monitors, Pathologists, Pharmacokineticists and Pharmaceutics to deliver high quality GLP and non-GLP in vivo study reports and, as needed, represent Genentech in meetings with regulatory authorities. Responsibilities include interdisciplinary project team membership, preparation and review of regulatory documentation, study reports and manuscripts, participation in toxicology and pharmacology initiatives, and other active cross-functional collaborations. Additional responsibilities include investigations into mechanisms of toxicity, proactive management of potential safety liabilities and communication of impact to teams and governance committees. Experience with cross-functional teams and capability to build productive cross-functional collaborations both within and external to Genentech are desired. ... |
Experienced | South San Francisco, California | |
| Jun 3, 2013 |
Study Data Manager (CDC II)
Clinical Data Management (CDM) is a department within the Biometrics function of the Product Development (PD) organization. CDM provides data management expertise to study management teams in PD and in gRED (Genentech Research & Early Development).
RESPONSIBILITIES:
The Study Data Manager (SDM) is a core member of Study Management Teams and serves as the study data management contact at the study and/or program level, providing expert guidance to program teams. The Study Data Manager leads the CDM study team and maintains oversight of all study start-up, study conduct and study close-out data management issues, activities and deliverables for one or more studies. The SDM interacts regularly with Clinical Data Management groups to ensure that project objectives are understood and met and provides technical coaching and mentoring on data management activities to colleagues. The SDM also performs the following: provides early strategic input into protocol design focused on data management issues; leads the development of eCRFs and database development and testing specifications by interacting with other functional area representatives; responsible for the oversight of all data review and cleaning activities involving close interaction with project clinical research professionals; responsible for the implementation of standards within Study Data Management across one or more CDM study teams; develops and executes ad hoc database queries utilizing data review and query tools; manages projects resourced externally via contract research organizations or corporate partners; provides support to ensure that study conventions, processes, knowledge sharing and best practices exist across all studies within a program; participates in departmental discussion groups, formal working groups or special projects. ... |
Experienced | South San Francisco, California | |
| May 15, 2013 |
Quality Manager
Here is an opportunity to join Roche as a Quality Manager. This position is responsible for proactively ensuring that all GCP governed clinical activities within the department (PDG – Operations) are delivered to the highest standards of quality and efficiency in accordance with the appropriate Roche and industry requirements and regulations.
The Quality Manager promotes quality and compliance excellence within PDG Operations by embedding quality principles throughout the organization. This is achieved through:
Quality Management System (QMS) – You will be required to understand and maintain the QMS requirements for the business and develop and implement the QMS and monitor its performance. Ensure cross functional alignment and compliance through process documents - By analyzing/reviewing “to be” processed, forms, templates and related process documents and facilitate review and approval of process documents along with global and cross functional teams. The Quality Manager will coordinate the functional subject matter experts by scheduling review and implementation of new/revised process documents. Risk management strategy - Ensure strategic quality risk management activities are implemented and maintained and enable identification of key risks for escalation to study teams and senior management. Performance metrics - Develop and implement the most appropriate key performance indicators (KPIs) for the business and monitor their effectiveness and gather and report on the metrics which give performance data on the chosen KPIs. Compliance support - Provide timely GCP compliance support to personnel by answering questions and providing advice and facilitate escalation of compliance issues through the appropriate routes and with appropriate urgency. Additional duties include:
... |
Experienced | South San Francisco, California | |
| May 15, 2013 |
Sr. Quality Manager
The Senior Quality Manager is responsible for proactively ensuring that all GCP governed clinical activities in PDG (Product Development Operations) are delivered to the highest standards of quality and efficiency in accordance with the appropriate Roche and industry requirements and regulations.
The Senior Quality Manager leads quality and compliance excellence within PDG by embedding quality principles throughout the organization. This is achieved through:
Quality Management System - Analyze and drive the QMS requirements for PDG and Implement, review and manage the QMS and monitor its performance. Ensure cross functional alignment and compliance through process documents - Analyze/review “to be” processes, forms, templates and related process documents. Coordinate the functional subject matter experts by scheduling review and implementation of new/revised process documents and develop and maintain effective relationships with other departments to ensure that all controlled document review activities are executed efficiently and effectively. Risk management strategy - Implement, review and maintain strategic quality risk management activities and implement, review and maintain systems that enable identification of key risks for escalation to study teams and senior management. Performance metrics - Implement, review and report the most appropriate key performance indicators (KPIs) for the business and monitor their effectiveness Implement, review and maintain processes that enable oversight for PDG management and personnel on the metrics which give performance data on the chosen KPIs. Compliance support - Drive the compliance support process for PDG in order to create a compliant workforce and workplace based on Regulator’s requirements. Provide timely GCP and process compliance support to personnel by answering questions and providing advice manage the process for escalation of compliance issues through the appropriate routes and with appropriate urgency. Additional duties and responsibilities:
... |
Experienced | South San Francisco, California | |
| May 20, 2013 |
Epidemiologist
Position Purpose: Epidemiologists work under the supervision of a Global Epi TA Head to review, generate and interpret quantitative evidence on disease from observational data sources to strengthen decision-making and minimize risk throughout research and development. Major Responsibilities and Accountabilities:
Primary Skills/Features:
Communication:
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Experienced | South San Francisco, California | |
| Apr 3, 2013 |
Scientist - Small Molecule Discovery Toxicology
The Department of Safety Assessment at Genentech providesscientific leadership and plays an active role in the process of drugdevelopment from late-stage discovery through marketed products. We are seeking an Associate Scientist/Scientist in the Department of Safety Assessment to supportdrug discovery and development. This role will involve working in acollaborative team environment as part of the comprehensive safety assessmentof Genentech therapeutics by providing discovery and investigative toxicologysupport to early stage small molecule research programs.
Proactive risk assessment ofpotential toxicity issues related to undesired or exaggerated pharmacology,investigation or characterization of potential toxicity issues to enable smallmolecule lead optimization and candidate nomination.
In this role, the toxicologist willprovide representation to discovery project teams, which will include safetytarget assessments, strategic planning and designing, implementing andsupervising toxicology studies in support of compound lead optimization(e.g. in vitro toxicity screening, counter-assay development) and mechanisticinvestigations (development of hypothesis-driven research plans, in vitro or invivo model development and qualification, and scientific projectmanagement). This position will include staff supervision as needed andcontributing to the continued refinement of lead optimization andinvestigational strategies and identification of new technologies. Thediscovery toxicologist will interact closely with research scientists andSafety Assessment development toxicologists and pathologists to ensure thatdiscovery teams consider all of the appropriate strategic needs for candidateidentification with regard to toxicology issues, thus providing bettercandidate selection and characterization of toxicology issues at the time oftransition to early development. ... |
Experienced | South San Francisco, California | |
| May 28, 2013 |
Product Manager - ACTEMRA Medical Marketing
Franchise: ACTEMRA Immunology (Rheumatoid Arthritis and SJIA) The Medical Marketing PM/SPM will contribute to the development of key aspects of strategic brand planning, KOL strategy for ACTEMRA Immunology and SQ launch preparation. This individual will be responsible for liaising with cross-functional partners within Genentech and Roche who interact with key customers and thought leaders, specifically, Medical Affairs and Thought Leader Services. Specific areas of responsibility may include:
*****Position description & qualifications are written at the Sr. Product Manager level. Role may be filled at the Product Manager level***** ... |
Experienced | South San Francisco, California | |
| Mar 26, 2013 |
Manager / Sr. Manager Interactive Patient Marketing
Interactive Patient Marketing is a Center of Expertise made up of experienced marketers who partner with the brands to focus on improving patient outcomes. Through a deep understanding of the patient, we devise highly impactful, integrated initiatives to drive desired behavior. We measure to continually optimize our impact and influence. As a result of our work, patients are better served, ultimately enhancing Genentech’s profitability and leadership.
The Manager/Senior Manager, Interactive Patient Marketing defines and oversees marketing programs to consumers, patients, caregivers, communities and health care providers that use social influence, permission-based and relationship marketing techniques, cultural/literacy adaptation and integrated marketing technologies with the purpose of generating better and measurable patient outcomes for Genentech products/therapies. The Manager/Senior Manager, Patient Marketing role partners with brand marketing and works with key internal/external partners/stakeholders in the strategic positioning, design, development and implementation of patient marketing plans and tactics for the assigned GNE products and/or special projects/initiatives. This particular position will focus on supporting a to-be assigned brand(s) in the oncology / cancer therapeutic area. Key Accountabilities:
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Experienced | South San Francisco, California | |
| May 9, 2013 |
Senior Manager, Brand Protection
Brand Protection is a proactive initiative to protect patient safety, supply chain integrity and brand reputation by identifying and acting on individuals or entities that intend to mislead healthcare practitioners, caregivers, patients, trade organizations or the public at large for their own illegal gain. The Senior Manager, Brand Protection reports directly to the Director, Interactive Marketing and is responsible for overseeing the Brand Protection Core Team, managing key external partnerships, directing ongoing surveillance, executing the communication strategies, analyzing the impact of these entities and reporting initiative progress to Commercial leadership. MAJOR RESPONSIBILITIES:
CAPABILITIES:
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Experienced | South San Francisco, California | |
| Apr 12, 2013 |
Sr. Product Manager - Lucentis Promotions
Franchise: Lucentis Please Note: Position description and requirements are written at the Sr. Product Manager level however role may be filled at the Product Manager(E4) level. The Product Manager (PM/SPM), Lucentis Promotions will contribute to the execution of Lucentis’ brand strategy and tactical plan, with a focus on physician promotional marketing. This person will leverage experience working with Promotional Review Committees (PRC) in order to ensure development of compliant and effective promotional tactics and effective pull-through of these tactics in the field. Additionally, this PM/SPM will develop promotional tactics and support field execution in a competitive environment so strategic insights will be important to success in this role. The PM/SPM will need to collaborate with a broad range of cross functional teams as well as the field force and be able to effectively manage various external vendors and agencies. Example Duties and Responsibilities:
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Experienced | South San Francisco, California | |
| Mar 29, 2013 |
eMarketing Manager / Sr. Manager
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Experienced | South San Francisco, California | |
| Jun 6, 2013 |
Senior Market Planning Manager (with direct reports)
Market Analysis & Strategy participates in commercial planning efforts by providing objective, in-depth information about Genentech's current and future markets, product performance, customers and competitors. Market Planning teams identify critical business issues and opportunities for growth; collaborating with various Genentech cross-functional teams to embed an external market point-of-view into the strategic direction of Genentech. Senior Market Planning Managers act as the lead market planner on Market Planning projects; providing assigned business partners and other internal partners/stakeholders with unbiased, objective, cumulative and in-depth information regarding current and future markets, product performance, customers and competitors.
Senior Market Planning Managers may also have people management responsibilities for one or more direct reports. Opportunities in various therapeutic areas including BioOncology. Example Duties and Responsibilities:
... |
Team Leader | South San Francisco, California |
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