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451 jobs match your search criteria:
| Date | Job Title | Job Level | Location | |
|---|---|---|---|---|
| May 31, 2013 |
Clinical Specialist - Nephrology, San Francisco
Franchise: Rheumatology Territory: San Francisco The Clinical Specialist, Nephrology Sales manages and develops long-term relationships with physicians and other customers for the customer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) and their approved indications; helping external customers such as physicians, nurses, etc. learn about the benefits of the assigned GNE brand(s) in relation to the applicable therapeutic area/disease state. Duties and Responsibilities:
This position requires significant use of either a company provided or personal vehicle to perform the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business. ... |
Experienced | San Francisco, California | |
| May 2, 2013 |
Clinical Specialist - RA Franchise - Kingston, NY
Franchise: Rheumatology Product: Actemra, Rituxan RA Territory: Kingston, NY
The Clinical Specialist, Franchise Sales manages and develops long-term relationships with physicians and other customers for the customer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) and their approved indications; helping external customers such as physicians, nurses, etc. learn about the benefits of the assigned GNE brand(s) in relation to the applicable therapeutic area/disease state.
Reports to: Division Manager, Franchise Sales
Example Duties and Responsibilities:
NOTE: This position requires significant use of either a company provided or personal vehicle to perform the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business. ... |
Experienced | Kingston, New York | |
| May 9, 2013 |
Clinical Specialist - Rituxan RA Key Account Specialist - N. Minnesota, N. Dakota
Franchise: Rheumatology Product: Rituxan RA Territory: N.Minnesota / N. Dakota
The Clinical Specialist, Franchise Sales manages and develops long-term relationships with physicians and other customers for the customer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) and their approved indications; helping external customers such as physicians, nurses, etc. learn about the benefits of the assigned GNE brand(s) in relation to the applicable therapeutic area/disease state.
Reports to: Division Manager, Franchise Sales
Example Duties and Responsibilities:
NOTE: This position requires significant use of either a company provided or personal vehicle to perform the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business. ... |
Experienced | Minneapolis, Minnesota | |
| May 23, 2013 |
Clinical Specialist Xolair Lower Manhattan
Franchise: Xolair Territory: Lower Manhattan (includes Manhattan, Brooklyn and Staten Island) The Clinical Specialist, Xolair Sales manages and develops long-term relationships with physicians and other customers for the customer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) and their approved indications; helping external customers such as physicians, nurses, etc. learn about the benefits of the assigned GNE brand(s) in relation to the applicable therapeutic area/disease state. Reports to: Division Manager, Xolair Sales Example Duties and Responsibilities:
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Experienced | New York, New York | |
| May 28, 2013 |
Clinical Specialist, Avastin - Denver, CO
The Clinical Specialist, Franchise Sales manages anddevelops long-term relationships with physicians and other customers for thecustomer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) andtheir approved indications; helping external customers such as physicians,nurses, etc. learn about the benefits of the assigned GNE brand(s) in relationto the applicable therapeutic area/disease state.
Reports to: Division Manager, Franchise Sales
Example Duties andResponsibilities: *Responsible for meeting or exceeding assigned sales targets *Develops robust territory business plans *Develops strong and long-term relationships with customersin all assigned accounts *Presents the assigned GNE brands in a professional,compliant, ethical and effective manner; helping external customers understandthe benefits and use of GNE brands *Monitors operating costs and compliance with territorybudget *Complies with all laws, regulations and policies thatgovern the conduct of GNE activities *Business travel, by air or car, is regularly required ... |
Experienced | Denver, Colorado | |
| May 22, 2013 |
Clinical Specialist, Avastin - Kansas City, KS
The Clinical Specialist, Franchise Sales manages anddevelops long-term relationships with physicians and other customers for thecustomer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) andtheir approved indications; helping external customers such as physicians,nurses, etc. learn about the benefits of the assigned GNE brand(s) in relationto the applicable therapeutic area/disease state.
Reports to: Division Manager, Franchise Sales
Example Duties andResponsibilities: *Responsible for meeting or exceeding assigned sales targets *Develops robust territory business plans *Develops strong and long-term relationships with customersin all assigned accounts *Presents the assigned GNE brands in a professional,compliant, ethical and effective manner; helping external customers understandthe benefits and use of GNE brands *Monitors operating costs and compliance with territorybudget *Complies with all laws, regulations and policies thatgovern the conduct of GNE activities *Business travel, by air or car, is regularlyrequired... |
Experienced | Kansas City, Kansas | |
| May 28, 2013 |
Clinical Specialist, Avastin - Los Angeles N, CA
The Clinical Specialist, Franchise Sales manages anddevelops long-term relationships with physicians and other customers for thecustomer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) andtheir approved indications; helping external customers such as physicians,nurses, etc. learn about the benefits of the assigned GNE brand(s) in relationto the applicable therapeutic area/disease state.
Reports to: Division Manager, Franchise Sales
Example Duties andResponsibilities: *Responsible for meeting or exceeding assigned sales targets *Develops robust territory business plans *Develops strong and long-term relationships with customersin all assigned accounts *Presents the assigned GNE brands in a professional,compliant, ethical and effective manner; helping external customers understandthe benefits and use of GNE brands *Monitors operating costs and compliance with territorybudget *Complies with all laws, regulations and policies thatgovern the conduct of GNE activities *Business travel, by air or car, is regularly required ... |
Experienced | Los Angeles, California | |
| May 20, 2013 |
Clinical Specialist, Pegasys - NY Metro
Clinical Specialist |
Experienced | New York, New York | |
| May 9, 2013 |
Clinical Specialist, Tarceva/Zelboraf - Knoxville or Asheville
Clinical Specialist, Tarceva/Zelboraf
Knoxville, TN or Asheville, NC The Clinical Specialist, Franchise Sales manages and develops long-term relationships with physicians and other customers for the customer accounts in the assigned territory. As such, Clinical Specialists represent the assigned GNE brand(s) and their approved indications; helping external customers such as physicians, nurses, etc. learn about the benefits of the assigned GNE brand(s) in relation to the applicable therapeutic area/disease state. Reports to: Division Manager, Franchise Sales Example Duties and Responsibilities: *Responsible for meeting or exceeding assigned sales targets *Develops robust territory business plans *Develops strong and long-term relationships with customers in all assigned accounts *Presents the assigned GNE brands in a professional, compliant, ethical and effective manner; helping external customers understand the benefits and use of GNE brands *Monitors operating costs and compliance with territory budget *Complies with all laws, regulations and policies that govern the conduct of GNE activities *Business travel, by air or car, is regularly required ... |
Experienced | Knoxville, Tennessee | |
| May 7, 2013 |
Clinical Trial Manager II, gRED
Purpose: The Genentech Research and Early Development (gRED) Senior Clinical Trial Manager (Sr. CTM) provides leadership to one or more global Study Teams within an early development program(s). The Sr. CTM is accountable for activities ensuring high quality deliverables are within budget and timelines. Primary Accountabilities and Responsibilities: • Independently lead cross-functional Study Team within Clinical Operations with minimal oversight from the CPL • Accountable for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budgets • Responsible for vendor selection and management including CRO, IVRS, central lab, imaging vendor • Provide input to the program budget and is accountable for managing overall study budget • Identify and track timelines, milestones, critical study activities, issues and budget and provide regular updates to the Study Team and CPL as appropriate • Partner with CPL to develop and/or present at project teams and management review bodies • Ensure relevant functional groups provide input to and participate in developing and finalizing Study Team level documents and meet Study Team level deliverables within timelines • Conduct protocol and site feasibility assessments • Provide drug supply assumptions to clinical planning team • Delegate and oversee study activities assigned to Clinical Operations as applicable • Provide support, mentoring, and study-specific training to Clinical Operations staff • Network and share best practices with colleagues to ensure optimal efficiency and consistency in Clinical Operations • Participate in initiatives and/or activities as assigned These statements are not intended to be an exhaustive list of all responsibilities, duties, and skills required of people assigned to this job, but are instead intended to describe the general nature and level of the work. Different levels of responsibilities and accountabilities may be assigned to take account of the skills capabilities and experience of the individual. ... |
Experienced | South San Francisco, California | |
| Apr 25, 2013 |
Clinical Trial Manager II-gRED
The Genentech Research and Early Development (gRED) Clinical Trial Manager (CTM) provides support and/or leadership to one or more global Study Teams within an early development program(s). The CTM is accountable for activities ensuring high quality deliverables are within budget and timelines.
Primary Accountabilities and Responsibilities:
• Support cross-functional Study Team within Clinical Operations with minimal oversight from the Sr. CTM and/or CPL • Responsible for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget • Responsible for vendor selection and management including CRO, IVRS, central lab and imaging vendor • Provide input to the study budget and is responsible for managing assigned vendor budget(s) • Under the leadership of the Sr. CTM, takes responsibility for agreed operational aspects (e.g., vendor management, drug supply management) • Identify and track timelines, milestones, critical study activities, issues and budget and provide regular updates to the Study Team and CPL as appropriate • Partner with CPL to develop and/or present at project teams and management review bodies • Conduct protocol and site feasibility assessments • Provide support, mentoring, and study-specific training to Clinical Operations staff • Network and share best practices with colleagues to ensure optimal efficiency and consistency in Clinical Operations • Participate in initiatives and/or activities as assigned
Responsibilities and Accountabilities When Leading a Study:
Depending on skill level and study design, CTM may lead Study Team, including obtaining agreement on project timelines, study objectives and goals.
• Ensure relevant functional groups provide input to and participate in developing and finalizing Study Team level documents and meet Study Team level deliverables within timelines • Accountable for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budgets • Provide input to the program budget and is accountable for managing overall study budget • Delegate and oversee study activities assigned to Clinical Operations Study Team as applicable • Provide drug supply assumptions to clinical planning team
These statements are not intended to be an exhaustive list of all responsibilities, duties, and skills required of people assigned to this job, but are instead intended to describe the general nature and level of the work. Different levels of responsibilities and accountabilities may be assigned to take account of the skills capabilities and experience of the individual. ... |
Experienced | South San Francisco, California | |
| Mar 23, 2013 |
Commercial Compliance Specialist / Sr. Compliance Specialist
Genentech's Commercial Compliance Operations (CCO) group, part of the broader Commercial Business Operations (CBO) organization, designs, implements, and owns business processes and systems needed to maintain compliance with state and federal laws and Genentech policies governing our interactions with healthcare professionals (HCPs) and related entities. The Transparency and Aggregate Spend Operations arm within CCO is principally responsible for tracking, monitoring, managing and reporting on Genentech's overall aggregate spend with the healthcare community to achieve transparency as defined by the Healthcare Compliance Office (HCO). To support this work, the group owns the Aggregate Spend Management system and related tools which provide automation and processes to enable the aggregating, self-monitoring, corrective action and internal and external reporting for transparency requirements. The group also owns and maintains processes for Fair Market Value payments to physicians, speaker program compliance, vendor registration for field personnel, and other processes supporting healthcare compliance. In addition, the group serves as an important conduit with the rest of the Commercial Operations organization to ensure a culture of compliance through well-thought out, actionable and achievable compliance processes. Given the nature of this group's work, they communicate and interface with a host of internal cross-functional partners, both within Commercial and with IT and other Genentech functions, and develop and implement business processes, systems and tools to support fully compliant and efficient management and reporting associated with Genentech's aggregate spend program. CCO Specialists track, monitor, manage and report Genentech's aggregate spend with Healthcare Professionals (HCPs) and organizations, as well as play an active role in the development of associated business processes, systems and tools. They employ a variety of data analysis techniques and direct junior team members in doing so, and distill analyses into useful information that helps drive business decisions. CCO Specialists also work with their manager in developing training/development programs and initiatives for CCO, preparing and delivering senior management presentations on strategic or complex issues and leading strategic projects. Incumbents in the CCO Specialist, role, as all other employees, are fully accountable for compliance with all laws, regulations and policies that govern the conduct of GNE activities. As a leader in the compliance area, the CCO Specialist demonstrates full knowledge and commitment to all applicable policies, monitors adherence to company policies and guidelines and acts according to established procedures to ensure all issues are addressed and resolved as required. Key Accountabilities: Commercial Compliance Operations Specialists are generally expected to:
Compliance, Knowledge & Skills |
Experienced | South San Francisco, California | |
| May 29, 2013 |
Competitive Intelligence Manager/Sr. Manager
The Competitive Intelligence Manager (“CIM”) participates actively in supporting Genentech's US commercial planning efforts by providing objective, in-depth information about current and future markets and competitive forces. The CIM acts as a strategic advisor to the US commercial teams with deep expertise in current and future competitive drivers in the marketplace as well as functional expertise in how to use CI to develop competitive strategies.
- Provide an objective commercial viewpoint based on an in-depth understanding and analysis of commercial, clinical, and scientific competitive information. Make recommendations on brand strategy that prepare the brand for a competitive marketplace. - Liaise with global CI counterparts to ensure up-to-date competitive intelligence and assumptions are shared with all appropriate US teams (includes congresses, news flashes, pipeline updates, therapeutic area landscape reviews) - Collaborate with brand to plan for competitor launches by co-planning local strategy wargames and supporting rigorous competitive readiness plans. - Lead competitive threat assessments to develop rigorous team assumptions about key competitors; ensure local assumptions are consistent with global assumptions. - Provide situational analysis support for quarterly business reviews, brand planning, launch readiness reviews, etc. - Field intelligence facilitation, including managed care teams - Work on innovative programs to increase the value of competitive intelligence processes and practice, and analyze the success of these programs. Liase across the broader Market Analysis & Strategy organization to deliver holistic analytic insights to the brands. Inform, communicate, and collaborate with MA&S partners. Positions may be filled at the Associate Manager, Manager or Sr. Manager level depending on experience. ... |
Manager | South San Francisco, California | |
| May 7, 2013 |
Compliance Specialist
Independently lead/participate on GMP compliance audits and identify GMP compliance gaps or risks. Provide GMP compliance expertise to internal and external customers. Perform tasks and work to achieve company goals and organizational objectives. · Follow company policies and procedures. · Set personal performance goals and provide input to departmental objectives. · Establish work priorities to meet targets and timelines. · Manage competing priorities and allocate, adjust, and optimize assigned department resources. · Serve as the Quality representative on cross-functional and multi-site teams. · Identify, design, and implement process and system improvements. · Manage department and cross-functional initiatives. · Apply advanced theory, technical principles, expert judgment, and cross-functional expertise to independently address a broad range of complex problems. · Troubleshoot and direct the resolution of Quality issues by fostering effective interdepartmental and cross-functional partnerships. · Serve as a technical subject matter expert (SME) in support of department functions. · Develop and train personnel and internal customers on relevant business processes. · Mentor junior personnel serving as a subject matter expert (SME) on Quality systems, processes and issues. · Collaborate and author department policies and procedures. · Make decisions that impact the goals and objectives of the department. · Notify Management of potential quality or regulatory issues that may affect product quality or regulatory compliance. · Sign documents for activities as authorized and described by Genentech policies, procedures and job descriptions. · Be accountable for behaviors as described in Genentech’s Core, Common, and Critical Competencies. · Perform any other tasks as requested by Management to support Quality oversight activities. · Participates in audits. Lead audits. Can develop audit findings that address individual gaps and system gaps. Can lead all “low risk” and most “high risk” area audits. Can participate on all high risk audits. Report requires little or no input from manager. May be asked to participate in meetings post audit to discuss unresolved issues with Senior Management. · Identifies gaps in corporate practices, policies and procedures and prioritizes based on current regulatory environment, guides and regulations. Leads teams to remediate or defend identified risks. Works with customers to develop CAPs and CAs for identified audit findings. Presents information on outcomes to Sr. Management. · Will be assigned compliance opinions. Needs no guidance from manager on resources / references. Opinion has depth and breadth and requires little or no input from Manager / review team. · Identifies gaps in corporate practices, policies and procedures. Leads efforts to remediate gaps. Write and or participate in corporate document development. · Participates in response development to regulatory inspection observations. Author responses if assigned. Acts as a SME for GMPC. · Participates in FDA Meetings. Acts as a SME for GMPC. · Participate as a GMPC representative in team meetings. Is a SME on compliance issues. Independently raises compliance issues with the team. Provides input on issues discussed informing manager of resolution. Communicates issues to manager as necessary. · Leads mock PAIs · Attends meetin... |
Experienced | South San Francisco, California | |
| Jan 18, 2013 |
Computational Biologist
The Department of Bioinformatics and Computational Biology in
Genentech Research is seeking a motivated individual to lead the development of software methods and infrastructure for the analysis of high-throughput biological data. This work will be in close collaboration with other computational researchers, as well as the broader community of Genentech scientists, who are together seeking novel therapies for unmet medical needs. Much of the software will be developed in R, as it is our primary data analysis environment. Interesting challenges include the scale of the data and the need for agility in a fast-paced, dynamic research environment. Publishing of methods and software is encouraged, and there is potential for collaboration with open-source projects. There is also opportunity for investigating open scientific problems in computational biology, such as variant calling, functional assessment of non-coding transcripts, and the relationship between copy number variation and expression.... |
Experienced | South San Francisco, California | |
| Jun 3, 2013 |
Computational Biologist
Genentech seeks a talented and highly motivated Computational Biologist to pursue research projects in collaboration with our Department of Oncology Biomarker Development. The primary focus is translation of complex biomarker data into useful diagnostic tools that can guide our understanding of drug activity in patient tumors and identify subsets of patients who may benefit from specific therapeutic interventions.
A successful candidate will work with interdisciplinary teams (including biomarker, clinical, biostatistics and bioinformatics scientists), will carry out data analysis and integration across various domains, and will develop novel methods for identifying diagnostic and prognostic biomarkers. Regular publication of scientific and methodological results is strongly encouraged. Finally, the successful candidate must be able to effectively present complex results in a clear and concise manner — to other bioinformaticians as well as to audiences without a computational or statistical background. ... |
Experienced | South San Francisco, California | |
| May 29, 2013 |
Computer Systems Quality - Internal Customer Relationship Management Internship
Support the implementation of Internal Customer Relationship Management process. Leverage knowledge from within PTQS to analyze customer interactions and develop a model for managing interactions between Computer Systems Quality and Informatics. Currently Informatics performs many activities which we rely upon to ensure the Right-To-Operate. Some of these activities directly support documented requirements for compliance while others do so less directly. Activities vary with complexity and so do the means and ways we interact with each other. Increased variability due to complexity results in less than optimal outcomes. A model for more predictable collaboration, interaction, and participation will improve efficiency, alignment, and customer relationships. An analysis of customer groups and interactions will need to be performed and conveyed via diagrams/charts. The diagrams and or charts will be used to understand the relationships in order to build a governance model for interactions. The governance model will need to minimally include a common understanding of agreed upon customer relationship, basic, concise overarching needs or expectations, and the foundation for: timely communication, appropriate involvement, proper engagement, performance measurement via tool, and decision making pathways. Key stakeholders will need to be identified. The governance model will be built with customer collaboration. As intern you will be responsible for coordination and scheduling of activities pertaining to the delivery of a governance model, customer relationship mapping/diagrams/charts, and a performance Indicator tool. This means one of the first items after orientation will be to understand the project and then start working on a timeline with actions and planned dates. Your responsibilities will also include gathering knowledge from PTQS SME experts in order to understand best methods for mapping customer relationships. Working together with PTQS and customer to complete the mapping/diagrams/charts. You will need to research performance tools available inside the company and externally and are responsible for providing a list of optional tools and a comparison of benefits for each tool based on the expected use. As intern you will draft a governance model framework as defined by the sponsor, which will subsequently be collaboratively detailed by the customers. You will be responsible for communication and follow up actions with stakeholders. Strong communication, presentation and organizational skills are necessary.
Customer Relationship Management (CRM) governance model |
Entry Level | South San Francisco, California | |
| Jan 31, 2013 |
Contract Manager
This position may be filled at a Contract Manager or Sr. Contract Manager level.
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Experienced | South San Francisco, California | |
| Apr 12, 2013 |
Contract Services Manager
Contract Services Manager Contract Services Managers are responsible for contract services (including contract set-up, membership and affiliation assignment and maintenance) and/or customer payments in accordance with accuracy and compliance requirements. Customer payments may include responsibilities, as assigned, for processing fees, rebates, discounts and chargebacks, as per the terms of each contract. Additionally, Contract Services Managers act as subject matter experts (SMEs) on SPCM Contract Operations processes, collaborating with Contract Operations partners and stakeholders in various meetings, initiatives and projects. Expertise in the processes, calculations, systems and Standard Operating Procedures (SOPs) that support contract services and customer payments is critical to success in this position. Contract Services Managers, by comparison to Associate Contract Services Managers, also have responsibilities for developing complex analyses and reports, reviewing from the work of less experienced team members, performing contract set-up and structure for other team members, managing Internal Control Over Financial Reporting (ICFR) tracking and monitoring activities, and leading projects to improve processes and procedures.
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Experienced | South San Francisco, California | |
| May 15, 2013 |
Custodian II
(Note: This description is not intended to be all-inclusive.) Perform outside maintenance tasks: |
Entry Level | Hillsboro, Oregon |
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