{"domain": "directsourcepro-rch.com", "user": "", "isWillingToRelocate": false, "isUserAuthenticated": false, "isUserETXCandidate": false, "isDomainETX": false, "isDomainVeteran": false, "signUpConfig": {}, "getHelpButton": {}, "isCareerPlannerEnabled": false, "enableRememberMeOption": false, "isMyApplicationsEnabled": false, "showVeteranEmployerSignUp": false, "enableUserPreferenceSelection": false, "isUserPreferenceApplied": false, "candidate": {"enc_id": 0, "fullname": "", "firstname": "", "lastname": "", "email": "", "phone": "", "location": "", "filename": null, "starred_positions": [], "resumeUrl": "", "onboardingCompleted": false, "isUserInPcsIjp": false}, "branding": {"page_title": "Contractor Positions for Roche and Genentech", "enableTalentNetwork": 1, "showJobId": 1, "hideSearchPanelHeader": true, "homePageHeroBanner": {"title": "Contractor Positions for Roche and Genentech Powered by PRO Unlimited", "image": "https://static.vscdn.net/images/careers/demo/directsourcepro-rch/New+Roche+image", "color": "#000000"}, "privacyLink": "https://eightfold.ai/privacy-policy/", "privacy": {"text": "<div class='main-container'><p>Please confirm that you agree to the <a href= https://cloud.kapostcontent.net/pub/15c2e367-3926-47cd-b537-c22ed1191720/directsource-pro-privacy-policy?kui=IWeABt_VHYAgW78OUaTwIQ target='blank'>Data Privacy Policy.</a></p></div>", "button": "Confirm", "title": "Data Privacy Policy"}, "companyName": "Roche", "navBar": {"color": "#FFFFFF", "image": "https://static.vscdn.net/images/careers/demo/directsourcepro-rch/New+Roche+generic+logo", "link": "https://directsourcepro-rch.prounlimited.com/careers", "background": "#FFFFFF", "title": "Roche"}, "custom_style": {"font": "https://fonts.googleapis.com/css?family=Open%20Sans", "css": ".nav-item a { color: #fff !important;} .refer .user-name { color: #fff !important; } \n.upload-resume-modal {overflow: scroll !important;\n} \n.hero-image {height: 400px !important;} .upload-resume-modal .privacy-agreement p {text-align: left !important; display: -webkit-box !important;\n\n list-style-position: inherit !important;\n text-indent: initial !important;\n ul {list-style-type: none; !important;} li {\n position: relative !important;\n left: -10px !important; display:block !important; margin: 0 !important; padding: 0 !important; margin-bottom: 5px !important; }} .upload-resume-modal .privacy-agreement {\n width: -webkit-fill-available !important;\n float: left !important;\n margin: 0 !important;\n display: inline-block !important;\n font-family: 'Helvetica', 'Arial', sans-serif !important;\n font-size: 11pt !important;\n line-height: 20px !important;\n margin-bottom: 20px !important;\n}.join-tn-link {color: #333333 !important;}.jumbotron h1 {color: #000000 !important;} .jumbotron h1 {text-align: center !important; color: #000000 !important} .jumbotron h1 {margin-top: 100px !important}.jumbotron h1{padding-left: 25px !important;}, .position-title line-clamp line-clamp-2 {color: #0066CC !important;}, .position-apply-button{background: #0066CC !important;} .fixed-top{text-align:right !important; padding-right: 20px !important} .navbar img{padding-right: 30px !important} .navbar {position:fixed; z-index: 99999; }"}, "custom_html": {"page-footer": "<p className='body-text-2'><a title='Visit Eightfold.ai homepage' target='_blank' rel='noopener noreferrer' style={{ color: 'black' }}><img src='https://static.vscdn.net/images/pro_direct_source.svg' alt='' width='100' height='11' align='middle' style='margin-bottom: 3px'/> &thinsp; %(text)s PRO Unlimited & eightfold.ai</a> </p>", "page-footer-text": "powered By"}, "hideJobCart": false, "recaptcha_enabled": 0}, "positions": [{"id": 137451307082, "name": "Clinical Trial Leader III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 1, "department": null, "business_unit": "Unknown", "t_update": 1656632532, "t_create": 1656632398, "ats_job_id": 137451307082, "display_job_id": 137451307082, "type": "ATS", "job_description": "Description: The Genentech Research and Early Development (gRED) Global contract Clinical Trial Leader (cCTL) is accountable for the strategic planning and execution of assigned early development global clinical trials [includes First-in-Human, Phase Ib, and other signal-seeking Phase I trials, and evidence of activity, proof-of-concept, dose-ranging, dual New Molecular Entity (NME), and other types of Phase II trials] under the direction of the Sr. Global Clinical Trial Leader (Sr. CTL). The cCTL is a member of one or more cross-functional Protocol Execution Teams (PETs). These complex programs focus on the rapid development of NMEs with limited clinical data, and as such, require implementation of novel and highly flexible global operational strategies to support exploratory hypotheses, including biomarkers and diagnostics. The cCTL enables the efficient delivery of global clinical studies, under the leadership of the Sr. CTL.", "stars": 0.0, "medallionProgram": null}, {"id": 137451970970, "name": "Research Associate III", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660317903, "t_create": 1660317769, "ats_job_id": 137451970970, "display_job_id": 137451970970, "type": "ATS", "job_description": "Duties: The successful candidate will be responsible for mammalian cell culture and transient transfection for recombinant protein expression in HEK293 cells. The qualified candidate will support expression and purification of extracellular vesicles to support R&D efforts. Skills: Experience in aseptic techniques, mammalian cell culture, protein characterization assays, including SDS-PAGE, Western blot is a must. Experienced in tangential flow filtration and high-throughput expression screening Familiarity with recombinant membrane protein expression, purification and stable cell line generation are a plus. Good communication and attention to detail, team-oriented and collaborative nature. Education: The successful candidate must have a BS or higher in Cell Biology, Biochemistry, Structural Biology or a related laboratory discipline with 2-5 years of industry experience in mammalian protein expression.", "stars": 0.0, "medallionProgram": null}, {"id": 137451772308, "name": "Research Associate III", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660069172, "t_create": 1660068757, "ats_job_id": 137451772308, "display_job_id": 137451772308, "type": "ATS", "job_description": "Description: Responsible for conducting research and other scientific activities to support Ventana projects. Exercises technical expertise and discretion in the design, execution and interpretation of experiments that contribute to project strategies. Prepares technical reports, summaries, protocols and quantitative analyses. Presents and discusses results of experiments within department and project team. Maintains high level of professional expertise through familiarity with scientific literature and may participate in conferences and professional societies. Follows company policies and procedures. Maintains complete and accurate laboratory documentation and electronic files. May act as principal investigator in conducting own experiments. Experience: Experience in microscopy, imaging systems, computer programming (e.g. Python) a plus. Education: Bachelor Degree in scientific related field", "stars": 0.0, "medallionProgram": null}, {"id": 137451768517, "name": "Clinical Science Specialist", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660012799, "t_create": 1660012496, "ats_job_id": 137451768517, "display_job_id": 137451768517, "type": "ATS", "job_description": "Description: In this role, the successful candidate will be able to independently collect, organize, and evaluate relevant scientific and technical information, including performance data, to prepare documentation in support of development and global registration of in vitro diagnostic medical devices. You will be responsible to critically review and summarize information and apply appropriate scientific principles to guide study planning and complete performance evaluation documentation. Peer-reviews device performance plans, study protocols, reports, and presentations. Coordinates cross-functional review and approval of documents in the document management system. Stays informed of performance evaluation requirements published or communicated by major Health Authorities (HAs). ESSENTIAL RESPONSIBILITIES: Conducts scientific literature reviews, objectively evaluates performance data, and prepares documentation for in vitro diagnostic products in support of product development and global registration. Documentation may include intended use statements, clinical validation plans, pre-submissions to the US FDA, performance evaluation documentation supporting compliance with the European IVDR (scientific validity reports, clinical performance reports, performance evaluation reports), as well as product instructions for use. Demonstrates understanding of intended uses of in vitro diagnostics and their application in clinical practice and applies this understanding to critical review of data and preparation of plans and reports. Peer-reviews documentation to ensure high quality with regard to scientific content, organization, clarity, accuracy, format, consistency, and adherence to regulatory and internal guidelines. Coordinates timely review and approval of documents within the document management system. Works with a cross-functional team (eg, Regulatory Affairs, Development, Medical Office, Quality, Marketing) to ensure timely completion and approval of clinical evidence documentation required for product registration. Miscellaneous duties and special projects as assigned, including deliverable tracking, process improvement, development of document templates and educational tools. Tracks progress of assigned deliverables to ensure timelines and other project team needs are met. Skills: Minimum of 2 years' experience in study design, data interpretation, and report writing for clinical or non-clinical studies. Experience writing reports for regulatory submissions and marketing applications is a plus. Experience in the in vitro diagnostic device industry, and/or immunohistochemistry, histology, cancer biology/oncology is desirable. Knowledge, Skills, and Abilities: Must have excellent writing skills and the ability to communicate correctly and effectively in English, and to use medical terminology accurately. Ability to quickly acquire and apply understanding of in vitro diagnostic device portfolios, business objectives, technical skills, clinical data/evidence. Knowledge of biomarker characterization, diagnostic testing laboratory workflow, histology, immunohistochemistry, and molecular biology preferred. Ability to manage multiple projects, interact with multi-disciplinary teams, and operate within a fast-pace environment. Requires in depth working knowledge of software programs used to prepare documents (Microsoft Word, Adobe Acrobat Professional, EndNote) Knowledge of literature databases and methods for systematic literature review. Knowledge of statistical basis for diagnostic device performance characteristics preferred. Ability to quickly develop expertise in the company's internal document management system. Be passionate about improving the lives of all patients afflicted with cancer.", "stars": 0.0, "medallionProgram": null}, {"id": 137451768505, "name": "Quality Engineer Associate", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660012248, "t_create": 1660012121, "ats_job_id": 137451768505, "display_job_id": 137451768505, "type": "ATS", "job_description": "Description: Applies intensive and diversified knowledge of design principles, practices and implementation in complex systems and assignments. General responsibilities include design concept generation, participating in design reviews, development and testing to assess performance against design specification; reliability testing, and assessment of system interactions. Makes independent decisions. Assist in the development of manufacturing processes and troubleshooting issues to determine root cause and possible engineering solutions. Responsibilities: Learns to use company concepts, policies and procedures, familiar with and follows standard practices. Normally receives detailed directions on all work. Makes suggestions to improve work processes. Assists in reducing to practice patentable inventions. Works on projects of moderate scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Participates in technical team activities. Presents and discusses data within group. Monitors work to ensure quality, and continuously promote Quality First Time. Other duties as assigned by management. Qualifications: To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities. Formal Training/Education: Bachelor's Degree or equivalent in a directly related discipline. (Required) Experience Entry level 2 years of related experience (preferred). Knowledge, Skills and Abilities Knows basic and some specialized engineering techniques. Familiar with searching technical literature. Skilled with use of word processing, spreadsheets, graphical and presentation software applications.", "stars": 0.0, "medallionProgram": null}, {"id": 137451768482, "name": "Research Associate", "location": "Dixon, CA", "locations": ["Dixon, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660011983, "t_create": 1660011877, "ats_job_id": 137451768482, "display_job_id": 137451768482, "type": "ATS", "job_description": "Description: The Molecular Biology department seeks a motivated laboratory researcher who will assist in the discovery of groundbreaking therapeutics by supporting the primary research of several hundred internal customers. The responsibilities include processing samples in the laboratory (both manually and via laboratory robotics), analyzing and performing quality control of genetic data, and helping to evaluate and implement new technologies. Applicants should have a learning mindset, be able to work in a fluid and diverse environment and possess a strong desire to participate in research support efforts while feeling comfortable working primarily in a laboratory setting. Skills: Basic understanding of PCR, quantitative/real-time PCR (TaqMan; 5' nuclease assay), and other nucleic acid amplification and detection techniques. You should demonstrate the ability to create basic PCR and qPCR assays. High attention to detail Communicate effectively The candidate's schedule must be flexible A more qualified candidate would also have functional knowledge regarding routine mammalian genetic constructs used in genome engineering, such as conditional knock-out models employing the Cre-Lox system. Education: Bachelor's degree preferably in Life Sciences or engineering, with one to two years' job experience in an academic or industrial research laboratory (university and class experience does not qualify)", "stars": 0.0, "medallionProgram": null}, {"id": 137451768477, "name": "Full Stack Developer / Solution Architect", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660011737, "t_create": 1660011626, "ats_job_id": 137451768477, "display_job_id": 137451768477, "type": "ATS", "job_description": "Description: Development Sciences Informatics (DSI) is seeking a talented and experienced software engineer / solution architect to design and develop cloud-based data centric software applications. The software needs to be flexible and scalable to ingest, manage and process petabyte of heterogenous scientific data to enable scientific research and drug discovery. Major responsibilities: Design client-side and server-side architecture Perform code review to ensure high quality software Build the front-end of applications through appealing visual design Develop and manage well-functioning databases and applications Write effective APIs Create security and data protection settings Write technical documentation Work with data scientists and analysts to improve software Requirements and skills: Proven experience as a Full Stack Developer or similar role Experience with cloud technologies, preferably Amazon AWS Knowledge and adherence to best software development practice Knowledge of multiple front-end languages and libraries (e.g. JavaScript, HTML/ CSS) Knowledge of multiple back-end languages (e.g. Java, Python) Knowledge of Java and JavaScript frameworks (e.g. Spring, Angular, React, Node.js) Familiarity with databases (e.g. PostgreSQL, ElasticSearch), and UI/UX design Good communication and teamwork skills Great attention to detail An analytical mind Education: Degree in Computer Science, Statistics or relevant field", "stars": 0.0, "medallionProgram": null}, {"id": 137451768383, "name": "Scientific Researcher", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660011402, "t_create": 1660011243, "ats_job_id": 137451768383, "display_job_id": 137451768383, "type": "ATS", "job_description": "Description: The Clinical Pharmacology (CP) Scientific Researcher is responsible for the delivery of PK/PD analyses and reports for their assigned development project[s], in order to ensure that appropriate dose/route/schedule decisions are made for the patients. The CP Scientific Researcher typically works under the supervision of a CP Scientist, in order to deliver the PK/PD elements of the agreed CP strategy. The CP Scientific Researcher works closely with colleagues in data programming, biostatistics and or infrastructure to facilitate the timely preparation and transfer of data sets containing PK/PD and critical patient demographic and treatment data for analyses. Performs other duties as assigned. Skills: Familiarity with quantitative approaches in drug development, working knowledge of or a strong desire and ability to learn data programming tools (eg. NONMEM, WinNonlin, Berkeley Madonna, R, S-Plus, SimCYP, GastroPlus) and the ability to plan, organize and perform PK/PD data analyses. Working knowledge of statistical approaches as they apply to clinical study design & analysis. Working knowledge of relevant disease areas. Communication Skills: The CP Scientific Researcher requires strong communication skills, both written and oral, in order to deliver high quality protocols, regulatory documents, documents for team and management review, scientific manuscripts & posters for publication. Drug Development Knowledge: The CP Scientific Researcher should have a good knowledge of GCP and working knowledge of relevant regulatory guidelines. Leadership: Based on experience and ability, the CP Scientific Researcher may lead CP teams, project sub-teams and represent CP at cross-functional project teams. Education: BA or BS in Statistics, Mathematics, Biology, Chemistry, Pharmaceutical Sciences, Biomedical Engineering, or related quantitative discipline is required", "stars": 0.0, "medallionProgram": null}, {"id": 137451768318, "name": "Business Systems Analyst", "location": "South San Francisco, CA", "locations": ["South San Francisco, CA"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1660011060, "t_create": 1660011000, "ats_job_id": 137451768318, "display_job_id": 137451768318, "type": "ATS", "job_description": "Description: Main Purpose of the Position: This position is part of Genentech's Environment, Health and Safety (EHS) function. EHS plays an essential role in protecting Genentech's right to operate and serving as a steward for the Genentech culture embracing prevention and problem solving to reduce risks and protect our people, environment and pipeline on our SSF campus and network of places. At Genentech, compliance is a shared responsibility with the business. The Junior Business Systems Analyst will support the delivery and maintenance of technology, data, and analytics solutions for the Environment, Health and Safety (EHS) group in Site Services. This position reports directly to the Director of EHS Strategy and Business Operations (SBO). Job Duties/Responsibilities: \u25cf Partners with internal stakeholders and colleagues within EHS, the business, and IT (up to Director level) to understand, define and deliver scalable technology, data, and analytics services and solutions to continuously improve the business. Aggressively achieves EHS business objectives by driving successful technology solutions. Contributes to shaping EHS culture via technology and data use within EHS and client groups. \u25cf Brings awareness of new approaches to technology and products, including opportunities to leverage data analytics and artificial intelligence to improve EHS business performance and integrating into EHS technology roadmap as applicable. \u25cf Supports implementation of the EHS technology roadmap and maintenance of existing infrastructure. Ensures technology properly reports EHS status, metrics, and insights. \u25cf Manages project delivery of technologies and supporting solutions to ensure compliance and a simplified end user experience. Tracks progress, identifies dependencies/constraints, evaluates risks and resolves issues. Communicates progress and challenges proactively with EHS Leadership Team and business stakeholders (typically up to the Director level). \u25cf Coaches and mentors others in utilization of technology and data. Competencies Identified for Success: \u25cf Outstanding analytical and organizational skills. Demonstrated ability to manage/track multiple projects of varying complexity and scope simultaneously. Possesses the curiosity and interest in re-evaluating existing designs and exercising independent judgment and decision making in solving issues and driving toward solutions. \u25cf Listens deeply to key stakeholders, considers their needs along with the needs of the business to make well-informed decisions. Possess a passion for digital innovation and commitment to a superb client experience. \u25cf Exceptional communication skills, including the ability to effectively develop clear and concise messages from complex data, present to EHS LT and staff, and quickly gain trust. Can translate data into actionable insights and communicate in a way that resonates\u2014inspiring people to care. \u25cf Excellent teamwork and collaboration skills. Proven ability to facilitate and lead effective cross functional and inter-departmental teams within a fast-paced, diverse and matrixed environment. This may include leading and/or participating in agile teams focused on creating value for the business. Qualifications: Education, Experience, Knowledge and Skills: (Minimum requirements) \u25cf Education: BA/BS in technology, engineering or business management, or equivalent work experience. \u25cf 0-3 years of experience in Information Technology (IT) Business Systems Analysis, Technology and EHS Applications including experience with IT software and database systems such as Tableau. \u25cf Experience in pharmaceutical, biotech, medical device or high tech industries is desired but not required. \u25cf Project management experience is highly desired. Proficient at organizing, managing and delivering solutions. \u25cf Working knowledge of LEAN/KANBAN/SCRUM software development methodologies is desirable. \u25cf Familiar with Cal OSHA, EPA, DOT, NIOSH, FDA and other regulatory requirements applicable to good clinical, laboratory, and manufacturing practices (GxP) and non-GxP environments highly desired. \u25cf This position is not eligible for relocation.", "stars": 0.0, "medallionProgram": null}, {"id": 137451738774, "name": "Data Coordinator I", "location": "Tucson, AZ", "locations": ["Tucson, AZ"], "hot": 0, "department": null, "business_unit": "Unknown", "t_update": 1659680499, "t_create": 1659679379, "ats_job_id": 137451738774, "display_job_id": 137451738774, "type": "ATS", "job_description": "Description: Assists Facilities organization to update Asset Management Database within existing CMMS; data capture and data entry, data quality assurance. Responsibilities Creates and updates assets data within Facilities CMMS. Supports Life Cycle Asset Management implementation by: Updating Asset Condition, lifetime, spare parts availability, acquisition costs. Ensures LoTo procedures are properly linked to facilities assets\u2019. Verifies accuracy of data in both Archibus and RAM. Assists as needed in developing a digital system to generate maintenance records. Conducts randomly monthly audits to confirm assets\u2019 location and data integrity Performs other similar duties as assigned. Other duties as assigned by management. Beginning November 15, 2021, Roche requires all US based contractors to be fully vaccinated against COVID-19 as of their start date. This requirement is a condition of contractor assignment at Roche, and it applies regardless of whether the position is located at a Roche campus or is fully remote. 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