Part time jobs south san francisco ca

Part time jobs south san francisco ca - • acts as sub-project manager for building technology with personal responsibility for:o applying decision making processeso defining roles and responsibilitieso gaining alignment with key stakeholders, customers and project management teamo management of sub-project to approved budget and scheduleo definition of prioritieso close coordination across disciplineso regular status updates including progress vs plan, risks, mitigationsincluding substantial contributions to overall project scope including:o options analysiso project planningo execution strategieso development of detailed schedule based on work breakdown structureo resourcingo estimating• executes deliverables in compliance with em, global standards and processes and all other roche guidelines and directives    • expresses relevant information timely, clearly and concisely to relevant stakeholders including adjusting communication style to the audience being addressed    • partners proactively with key customers, team members and stakeholders, while being open and approachable with a friendly, positive and professional attitude    • challenges the status-quo and develops creative solutions within the framework of global standards and processes    • leads proactive measures to achieve the specified goals in the event of deviations from the project plan    • manages a sub-project team including external contractors and gives clear guidance to the team in terms of technical solutions and/or business processes    • maintain ownership of assigned work-package within discipline through all project phases so that target functionality, quality and reliability are achieved    discipline specifics    • experience with facilities within the following areas: office and amenities, research and development (r&d), quality laboratory, commercial manufacturing and clinical manufacturing• experience in one or more of the following fields: electrical, black utilities, environmental and hvac. Works with pd medical directors/clinical development physicians, clinical operations, data management and potentially other groups to develop and communicate relevant medical inquiriesparticipates in safety meetings and tracks, analyzes and reports any potential safety eventsreviews, analyzes and discusses clinical study reporting documents with pd medical directors/clinical development physicians and various other groupstracks items for inclusion in protocol/icf amendments and works with other groups to ensure the timely and appropriate completion of protocol amendmentsassists pd medical directors/clinical development physicians in responding to ha inquiriessupports pd medical directors/clinical development physicians in preparing for internal/external meetings and presentationsworks closely with pd medical directors/clinical development physicians, clinical operations and other groups to close-out clinical studies, secure data and complete study reportingparticipates in the development and implementation of communications strategies to support existing and concluded studies. Global clinical development planningstays abreast of internal and external developments, trends and other dynamics relevant to the work of cd to maintain, at all times, a fully current view and perspective of internal/external influences and/or implications for the assigned therapeutic and disease area(s)as appropriate, participates in competitive intelligence and/or other market/industry assessment activities and projectsmaintains scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and kols, as well as multidisciplinary internal groups, including other groups in pd, research, business development, commercial operations, legal, etc.   key roles and responsibilities include:  serves as a member of one or more global cross-functional protocol execution team(s) (pets) through all study stages (start-up, conduct, close-out) to contribute to the accomplishment of studies outlined by the clinical development plan tracks budget, timelines, milestones, and critical study activities, identifies issues and proposes potential resolutions partners closely with clinical science in designing global clinical trial protocols and provides strategic operational input on protocol feasibility.