1,779 Results for

Principal Jobs in West Roxbury, MA

Jobs

Clinical Social Worker - Inpatient Psych UCSF Medical Center

San Francisco, CA

Maintain up to date knowledge of the full the spectrum of community resources, including referral processes, for discharge planning needs including basic needs (food, shelter), long term locked psychiatric facilities, residential care facilities and outpatient programs, clinics and providers. Under the general supervision of the Director of Clinical Services and as part of a multidisciplinary treatment team, the inpatient social worker's duties include but are not limited to psychosocial assessment, case management, individual and family therapy and crisis intervention for patients hospitalized on an acute psychiatric unit.

30+ days ago

Healthcare Regulatory Associate Attorney Jobot

San Francisco, CA

$260,000–$360,000 / year

Billable-hour framework: 2,000-hour annual bonus threshold, with market reporting indicating approximately 1,800 client-billable hours and up to 200 qualifying hours for pro bono and other approved activities. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.

9 days ago

Per Diem Primary Care Physician (Casual Employee) One Medical

SAN FRANCISCO, CA

Our seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.

9 days ago

Per Diem Family Nurse Practitioner or Physician Assistant (Casual Employee) One Medical

SAN FRANCISCO, CA

9 days ago

Per Diem Family Medicine Physician (Casual Employee) One Medical

SAN FRANCISCO, CA

Today

Per Diem Primary Care Nurse Practitioner or Physician Assistant (Casual Employee) One Medical

SAN FRANCISCO, CA

4 days ago

Senior Clinical Research Associate - Oncology Zp Group Llc

San Francisco, CA

$120,000–$145,000 / year

Keywords: Senior Clinical Research Associate, Senior CRA, Clinical Research Associate, Oncology Clinical Trials, Oncology Research, Phase II Clinical Trials, Phase III Clinical Trials, Clinical Monitoring, Independent Monitoring, Site Monitoring, Site Management, Clinical Operations, ICH-GCP, FDA Regulations, GCP Compliance, Clinical Trial Management, Source Data Verification, SDV, Source Data Review, SDR, CRF Review, Case Report Forms, Site Initiation Visits, SIV, Interim Monitoring Visits, IMV, Closeout Visits, COV, Investigative Sites, Study Start-Up, Patient Enrollment, Site Performance, Risk Management, Protocol Compliance, Clinical Development, Biotechnology, Biotech Sponsor, Pharmaceutical Research, CRO, Sponsor-Facing, Trial Execution, Site Oversight, Data Quality, Inspection Readiness, Regulatory Compliance, Oncology Studies, Clinical Research, Clinical Trial Oversight, Clinical Monitoring Visits, Site Relationships, Clinical Study Management. Responsibilities for the Senior Clinical Research Associate include: Independently monitoring Phase II-III Oncology clinical trials to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.

27 days ago

Sr Clinical Research Coordinator Clinical Research Network Office UCSF Medical Center

San Francisco, CA

Positions at Sr CRC level may perform expert and efficient integration of multiple complex programmatic activities, applying a sophisticated medical knowledge base, substantial leadership skills, and effectively working with a variety of internal (clinicians, investigators, clinical staff, administration, Institutional Review Board (IRB), human resources, contracts and grants) and external (industry sponsors, coordinating centers, FDA, NIH) stakeholders, exhibiting an in-depth knowledge of specific programs. The Sr CRC will perform independently or with general direction at the fully operational level of the series to execute, manage, coordinate research protocols, and train staff, as directed by the Principal Investigator (PI), Program Director, and Clinical Research Manager (CRM).The incumbent may have central responsibility for assisting with IRB approval and compliance, ensuring subject recruitment and adequate enrollment, executing research procedures, and developing site and study specific workflows.

29 days ago

Clinical Research Associate Integrated Resources, Inc

San Jose, California

Contractor

Works with clinical programmers, CRA, statistical programmers, biostatisticians and other clinical, DSPH, regulatory and project management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting. Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery.

20 days ago

Senior Clinical Research Associate Protagonist Therapeutics Inc

Newark, CA

$135,000–$150,000 / year

Support study vendor management by performing key activities as delegated by study CTM, including but not limited to: Participate in evaluation of new vendors (CROs, labs, central readers, EDC, etc.) by drafting and/or reviewing RFPs, analyzing responses and drafting work orders for select vendors • Manage the day to day interactions with select study vendor(s), such as a central or specialty lab including developing training materials, lab manuals and acting as first point of contact for issue and query escalation and resolution. Part of the clinical study team and takes a lead on execution by performing key activities as delegated by the Clinical Study lead, including but not limited to: Develop and/or review key study operational documents (e.g., study reference manual, laboratory and pharmacy manuals, data management plan, query generation, monitoring plan; review site audit reports) •.

30+ days ago

On-site Clinical Research Associate Protagonist Therapeutics Inc

Newark, CA

$125,000–$135,000 / year

The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs. Serves as the internal primary site operations lead, working with the Project Manager and CROs to achieve efficient study set-up and initiation, ongoing data monitoring all the way through successful study execution and site close-out.

14 days ago

Clinical Research coordinator/ Clinical Project Associate Integrated Resources, Inc

Foster City, California

Contractor

Clinical Research Coordinator/ Clinical Project AssociateThe position entails work under general supervision for routine tasks and with detailed instructions on new assignments. Assists with development of documents for site bindersAssembles and prepares distribution of site binders.

20 days ago

Senior Clinical Research Associate (level dependent on experience) CTI

San Francisco, California

For that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.

30+ days ago

Clinical Research Associate Neuralink Corp

Fremont, CA

$89,000–$148,000 / year

From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink's BCI technology for use in people! Your work will directly contribute to the planning, execution, and success of innovative trials, from the initial phases of study setup to hands-on clinical monitoring and site management.

30+ days ago

Senior Clinical Research Coordinator Cardiology UCSF Medical Center

San Francisco, CA

Reporting to Clinical Research Supervisor, the incumbent may have central responsibility for ensuring CHR approval and compliance, contract generation, negotiation and approval, subject recruitment, appropriate study testing, and adequate enrollment of multicenter clinical trials, longitudinal cohort studies, local investigator-initiated studies, and biorepository efforts; exercise strong administration and management leadership of clinical research, strong research coordination, and may lead experienced personnel to ensure optimal systems for efficiency, compliance, safety, financial oversight, and contractual expertise in negotiations and execution, as well as create and implement quality improvement processes. Positions at this level may perform expert and efficient integration of multiple complex programmatic activities, applying a sophisticated medical knowledge base, substantial leadership skills, effectively working with a variety of people and organizations at UCSF (clinicians, investigators, clinical staff, administration, Committee on Human Research, human resources, contracts and grants) and elsewhere (industry sponsors, coordinating centers, FDA, NIH), exhibiting an in-depth knowledge of specific programs.

28 days ago

Clinical Research Coordinator UCSF Medical Center

San Francisco, CA

The duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; recruit study participants; act as intermediary between services and departments while overseeing data management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; manage Investigator's protocols in the IRB/Institutional Review Board online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. Department Description: The UCSF Division of General Internal Medicine (DGIM) at Zuckerberg San Francisco General Hospital and Trauma Center (ZSFG) delivers innovative, comprehensive and complex primary medical care to San Francisco's vulnerable patients; carries out highly impactful translational research focused on generating new knowledge to improve the health of vulnerable populations; engages in meaningful policy work focused on reducing health disparities and ensuring access to care; and trains the next generation of physician leaders and researchers in the care of vulnerable and underserved populations.

30+ days ago

Senior Clinical Research Coordinator UCSF Medical Center

San Francisco, CA

On the drug-resistant tuberculosis cluster randomized pragmatic trial, the Senior CRC will report to the Principal Investigator and will have central responsibility for ensuring the overall coordination, administration, and monitoring of the trial, which includes close collaboration with academic research partners, public health officials, commercial entities, and non-governmental actors in multiple international settings. Clinical Trials/Research Project Management: Negotiate pre-trial agreements, budget, and supply chains; work with Research Services Analyst and Industry Contracts to execute agreements; set up ancillary departments, train staff as needed, assign tasks, create documentation, and ensure in-country research law compliance.

30+ days ago

Senior Clinical Research Coordinator, Liver Biorepository UCSF Medical Center

San Francisco, CA

Reporting to the Principal Investigator/Director, the incumbent has central responsibility for ensuring IRB approval and ongoing compliance for the biorepository and its protocols; managing consent, specimen accessioning, inventory, and chain-of-custody; coordinating biospecimen requests and material transfers; and building and maintaining the IELB website to communicate available samples, governance policies, and request procedures to the research community. Determine interest of groups in trial participation, assess ability to execute protocol safely and properly (analysis of infrastructure, staff, funding needs), negotiate pre-trial agreement and budget, work with Research Services Analyst and Industry Contracts to execute agreement, set up ancillary departments, train staff, assign tasks, create documentation, and ensure local and federal research law compliance.

30+ days ago

Clinical Research Coordinator HEMOC UCSF Medical Center

San Francisco, CA

Administrative duties may include: coordinating project schedules and team meetings; managing Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participating in the review and writing of protocols to ensure institutional review board approval within University compliance; helping assure compliance with all relevant regulatory agencies; overseeing study data integrity; implementing and maintaining periodic quality control procedures; maintaining all regulatory documents; participating in any internal and external audits or reviews of study protocols; and performing other research-related duties as assigned. The CRC's duties may include, but will not be limited to: recruiting research subjects (identification, determine eligibility and obtain consent of potential research participants); obtaining medical and health information from participants and abstracting information from electronic clinical records; administering surveys; conducting semi-structured interviews; overseeing participant payments; creating, cleaning, updating, and managing qualitative and quantitative datasets and reports; analyzing data using quantitative and qualitative methods; assisting in conducting literature reviews; participate in manuscript preparation and research result presentation.

30+ days ago

Clinical Research Coordinator Cardiology UCSF Medical Center

San Francisco, CA

Incumbent's duties may include, but will not be limited to, support the management of and coordinate the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, update, and manage databases and comprehensive datasets and reports; help to coordinate staff work schedules to ensure proper coverage; assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage PI's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval and University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPAA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms.

9 days ago

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Principal Jobs in West Roxbury, MA

Clinical Social Worker - Inpatient Psych UCSF Medical Center

Healthcare Regulatory Associate Attorney Jobot

Per Diem Primary Care Physician (Casual Employee) One Medical

Per Diem Family Nurse Practitioner or Physician Assistant (Casual Employee) One Medical

Per Diem Family Medicine Physician (Casual Employee) One Medical

Per Diem Primary Care Nurse Practitioner or Physician Assistant (Casual Employee) One Medical

Senior Clinical Research Associate - Oncology Zp Group Llc

Sr Clinical Research Coordinator Clinical Research Network Office UCSF Medical Center

Clinical Research Associate Integrated Resources, Inc

Senior Clinical Research Associate Protagonist Therapeutics Inc

On-site Clinical Research Associate Protagonist Therapeutics Inc

Clinical Research coordinator/ Clinical Project Associate Integrated Resources, Inc

Senior Clinical Research Associate (level dependent on experience) CTI

Clinical Research Associate Neuralink Corp

Senior Clinical Research Coordinator Cardiology UCSF Medical Center

Clinical Research Coordinator UCSF Medical Center

Senior Clinical Research Coordinator UCSF Medical Center

Senior Clinical Research Coordinator, Liver Biorepository UCSF Medical Center

Clinical Research Coordinator HEMOC UCSF Medical Center

Clinical Research Coordinator Cardiology UCSF Medical Center

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