Staff II Pharmacist - Hematology/Oncology Clinical Pharmacist UCSF Medical CenterStaff II Pharmacist - Hematology/Oncology Clinical PharmacistSan Francisco, CAThese include, for example, obtaining medication histories, reviewing and assessing medication profiles, providing drug information to patients and health care providers, collaborating with clinicians on drugs of choice and therapeutic plans, ensuring access to medications, educating patients on the proper use of medications, and ensuring that patients understand cautions, adverse reactions, and interactions related to their therapy. These services include, but are not limited to: drug procurement, storage, and security; safe, accurate and timely preparation and distribution of drugs; clinical pharmacy services for patients; development of drug use policies within the Medical Center; drug information services for clinicians and patients; and participation in technology assessment and quality assurance programs.
NewMgr, Clinical Nutrition I Compass Group USA IncMgr, Clinical Nutrition IHayward, CA$105,000–$120,000 / yearResponsible for managing daily clinical operations, ensuring regulatory compliance, supporting quality and patient care initiatives, mentoring dietitians, collaborating with multidisciplinary leadership, and driving operational excellence across multiple hospital locations. Compass Group employs over 3,000 RDNs across the United States, making us one of the nation's largest employers of Dietitians in a variety of settings: Hospitals and healthcare systems.
Senior Clinical Trials Manager (Biotech Oncology) Exelixis IncSenior Clinical Trials Manager (Biotech Oncology)Alameda, CA$172,000–$245,000 / yearApproaches problems and solutions with an enterprise mindset, considering broad impact to portfolio, regional, and global functions • Ability to study, analyze, and understand new situations and business problems and identify appropriate solutions • Curious in planning; agile in execution • Operationally excellent and drives others towards excellence • Resilient in the context of a rapidly changing environment • Organized with a systematic approach to prioritization. Education/Experience: • BA/BS in biological sciences or related field and a minimum of 9 years of related experience; or, • MA/MS in biological sciences or related field and a minimum of 7 years of related experience; or, • PhD/PharmD in biological sciences or related field and a minimum of 2 years of related experience; or, • Equivalent combination of education and experience.
Senior Clinical Trials Manager (Biotechnology, Oncology) Exelixis Inc.Senior Clinical Trials Manager (Biotechnology, Oncology)Alameda, CA$172,000–$245,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BA/BS in biological sciences or related field and a minimum of 9 years of related experience; or, MA/MS in biological sciences or related field and a minimum of 7 years of related experience; or, PhD/PharmD in biological sciences or related field and a minimum of 2 years of related experience; or, Equivalent combination of education and experience. SUMMARY/JOB PURPOSE: The Senior Clinical Trials Manager, Clinical Operations, combines end-to-end design, execution, and reporting of oncology clinical trials with leadership in study teams and across matrix teams.
Senior Clinical Research Scientist IINewRemote Berkeley California United States Remote Caribou Biosciences IncSenior Clinical Research Scientist IINewRemote Berkeley California United States RemoteBerkeley, CA$215,000–$230,000 / yearWe believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases. Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases.
Clinical Research Coordinator Surgery UCSF Medical CenterClinical Research Coordinator SurgerySan Francisco, CAKnowledge of UCSF and departmental policies for dealing with research payments and reimbursements; patient safety and confidentiality; packing/shipping infectious substances; database building/analysis, and data management within some of the following platforms: Access, Stata, SASS/ SPSS, and Teleform. Experience applying the following regulations and guidelines:The Protection of Human Research SubjectsGood Clinical PracticeHealth Insurance Portability and Accountability Act (HIPAA)IRB regulationsSafe shipping practices (IATA)Environmental Health and Safety TrainingFire Safety Training.
Sr. Clinical Trial Manager Structure Therapeutics IncSr. Clinical Trial ManagerSouth San Francisco, CA$171,000–$218,000 / yearIdentifies potential study issues/risks, escalates as needed and recommends/implements Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up. Minimum of 7+ years of related industry experience as a Clinical Research Associate or related function with increasing responsibility and scope Minimum of 3+ years study management experience in clinical and drug development Experience in selecting, managing, and overseeing sites, CROs, specialty labs and other service providers in global, multinational studies or programs.
Clinical Trial Manager Structure Therapeutics IncClinical Trial ManagerSouth San Francisco, CA$146,000–$185,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers budgets and proposals, conduct bid defense meetings, award services, negotiate, and execute complex agreements (e.g., CRO study-related collaboration agreements). The companys platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Sr. Clinical Trial Manager (Mp) Structure Therapeutics IncSr. Clinical Trial Manager (Mp)South San Francisco, CA$171,000–$218,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements). Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up.
Sr. Clinical Trial Manager (Ns) Structure Therapeutics IncSr. Clinical Trial Manager (Ns)South San Francisco, CA$171,000–$218,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements). Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up.
Sr. Clinical Trial Manager (Da) Structure Therapeutics IncSr. Clinical Trial Manager (Da)South San Francisco, CA$171,000–$218,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements). Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up.
Sr. Clinical Trial Management Associate Integrated Resources, IncSr. Clinical Trial Management AssociateFoster City, CaliforniaContractorInterfaces with individuals in other functional areas to address routine study issuesAbility to develop tools and processes that increase measured efficiencies of the projectMay be asked to assist in the training of CTMAs and CPAsAssists in CRO or vendor selectionCoordinates CROs or vendorsAssists in the setting and updating of study timelinesMust be able to participate in departmental or interdepartmental strategic initiatives under general supervisionAssists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepanciesMay conduct site evaluation, initiation, co-monitoring, and closeout visits in addition to routine monitoring visits, as requiredAssures site compliance with the protocol and regulatory requirementsDrafts and coordinates review of protocols, informed consents, case report forms and monitoring plansExcellent verbal, written, interpersonal and presentation skills are requiredKnowledge of FDA and or EMA Regulations, ICH Guidelines, and GCP governing the conduct of clinical studiesWorking knowledge and experience with Word, PowerPoint and ExcelQualificationsMinimum Education And ExperienceAt least 3+ years of experience and a BS or BA in a relevant scientific disciplineAdditional InformationKind Regards,Sabanaaz ShaikhClinical RecruiterIntegrated Resources, Inc. Clinical Trials Management AssociateDuration: 6 MonthsLocation: Foster City, CA, United StatesJob Responsibilities And SkillsMust meet all requirements for CTMA position and have demonstrated proficiency in all relevant areasMust be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and proceduresParticipates or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teamsMust be able to anticipate obstacles and proactively develop solutions to achieve project goalsMust have a general understanding of functional issues and routine project goals from an organizational perspectiveMay participate in abstract presentations, oral presentations and manuscript development.
NewClinical Social Worker Supervisor UCSF Medical CenterClinical Social Worker SupervisorSan Francisco, CADuties of this position include: recruiting, training, and evaluating staff (including initiating disciplinary proceedings as needed), leading team meetings, presenting for community partners and at conferences, collecting data for audits, helping with annual reports and program development, participating in Citywide Leadership Team Meetings, and completing other activities as needed. Coordinates closely with community partners.5YesOperates within budgetary parameters in the management and distribution of material and fiscal resources5YesParticipates in the performance of routine audits and accreditation licensing inspection readiness activities 100% (To update total %, enter the amount of time in whole numbers (without the % symbol - e.g., 15, 20) then highlight the total sum (e.g., 1%) at the bottom of the column and press F9.
Clinical Research Coordinator II Sutter HealthClinical Research Coordinator IISan Francisco, CA$43.34–$65 / hourTotal compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. Possess written and verbal communications skills to communicate with fellow team members, supervisors, patients, and other hospital personnel.
Sr. Clinical Research Associate (Da) Structure Therapeutics IncSr. Clinical Research Associate (Da)South San Francisco, CA$135,000–$150,000 / yearOverall management of selected clinical sites including acting as a point of escalation and oversight of CRO monitoring activities, which includes monitoring visit report review, contract and budget negotiations with clinical sites. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Senior Manager, Global Clinical Scientist (Cell Therapy) Bristol-Myers Squibb CoSenior Manager, Global Clinical Scientist (Cell Therapy)Brisbane, CA$173,390–$210,110 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Clinical Social Worker 2/3 - Per Diem UCSF Medical CenterClinical Social Worker 2/3 - Per DiemSan Francisco, CAThe Clinical Social Worker coordinates resources and services in response to a patient's psychosocial needs while collaborating with Case Managers, Nursing Staff, Medical Staff, and ancillary departments with the goal of supporting a timely and safe discharge and/or meeting the continuing care needs within the fiscal realities of the case. The CSW III (LCSW) has advanced clinical knowledge and skills and participates in leadership activities including advanced program planning, provision of educational programs, clinical supervision, consultation to the clinical team, other departments, and the community.
Clinical Social Worker 2 UCSF Medical CenterClinical Social Worker 2San Francisco, CAMINIMUM REQUIREMENTS: Master''s degree from an accredited school of social work, and possession of the requirements necessary for application for licensure as a clinical social worker as determined by the California Board of Behavioral Science Examiners; or an equivalent combination of education and experience; and knowledge and abilities essential to the successful performance of the duties assigned to the position; Demonstrated clinical experience in healthcare or behavioral health settings serving medically complex or vulnerable populations. The Clinical Social Worker II collaborates and coordinates with nephrology, nursing, case management, psychiatry, and ancillary services to address psychosocial factors that impact treatment adherence, patient safety, and health outcomes, and provides resources and services to address a patient's psychosocial needs.
ECM Clinical Manager (RN) VyncaECM Clinical Manager (RN)San Mateo, CaliforniaRemoteThe ECM Clinical Manager will communicate directly with ECM staff and occasionally with patients via telephone, telehealth, or during Interdisciplinary Care Team meetings (as needed) to discuss medication management/adherence, ensure appropriate follow-up with Primary Care Provider, Behavioral Health Provider, and other specialist(s). The ECM Clinical Manager will collaborate with the client’s broader care team (PCP, BH clinicians, etc.) to provide client advocacy, ensure that the clients receive needed services, and measure progress toward the goals outlined in their patient-centered individualized care plan.
Senior Clinical Outsourcing Manager (Remote Eligible) Denali Therapeutics IncSenior Clinical Outsourcing Manager (Remote Eligible)South San Francisco, CARemote$155,000–$202,000 / yearDirects and coordinates all clinical outsourcing needs; including vendor identification and selection, Request for Proposal (RFP) and Bid Defenses, negotiating SOW and budgets including change orders, co-manage all outsourcing budgets, performance metrics, and vendor oversight/governance. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.