Clinical Contracts Associate Integrated Resources, IncClinical Contracts AssociateFoster City, CaliforniaContractorContractual background - doesn't necessarily need to be in clinical research, but able to understand clinical contracts is importantPreviously seen people with experience in business administration, clinical research, business analysts that reviewed contractors, legal backgroundsNot looking for people with accounts payable backgroundPreviously worked in CRO or clinical sitesAdditional InformationFeel free to forward my email to your friends/colleagues who might be available. IT Life Sciences Allied Healthcare CRODIRECT # - (732)-844-8715Gold Seal JCAHO Certified for Health Care Staffing"INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)
Research Associate 2 NateraResearch Associate 2San Carlos, CA$74,800–$93,500 / yearYou will execute Next-Generation Sequencing (NGS) workflows, cell-free DNA (cfDNA) extraction, and library preparation, generating the high-quality data required to advance our clinical diagnostic assays. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.
Research Administration Manager UCSF Medical CenterResearch Administration ManagerSan Francisco, CA10% Leads the organization, planning, establishment and monitoring of fiscal budget control of contracts and grants administration, submissions, budgets, support documents, gifts, endowments and privately funded projects for faculty research programs and departmental operating budgets; Initiates and maintains ongoing, timely and effective communication with all relevant parties throughout the entire post-award process (e.g. This position will provide analytical and financial expertise and leadership for a team of Research Financial Analysts who support contracts and grant administration including post-award fund management activities associated with invoicing, forecasting, planning and managing of research portfolios, and closeout for federal, state, local, private sponsors, and clinical trials for the Hematology and Oncology Division.
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.
Clinical data manager Integrated Resources, IncClinical data managerFoster City, CaliforniaContractorWorks collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Bio banking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. QualificationsLead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experienceUnderstanding of clinical data management processesProject management experience of clinical trialsCommunication with cross-functional study team members
Clinical data Manager Integrated Resources, IncClinical data ManagerFoster City, CaliforniaContractorWorks collaboratively with biomarker clinical operations team members, biomarker scientists, biomarker statistical programming group, biomarker biostatistics group, biomarker clinical programming group, biobanking and sample management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking, and reporting. The ideal candidate should possess a BS degree or higher in a biomedical science or equivalent and minimum 3 years of relevant clinical data management experience and preferably along with biomarker or laboratory background and experience in a CRO or bio/pharmaceutical setting.
NewSenior Clinical Trial Manager - Job ID: 2013 Ascendis PharmaSenior Clinical Trial Manager - Job ID: 2013Palo Alto, CARemoteManages and/or supports vendor management for central laboratory, central IRB, central imaging, patient concierge services, and site payment systems including but not limited to: portal access management for sites and internal teams, report review, sample tracking, metrics review, document reviews and meeting participation. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Associate Director, Clinical Operations Protagonist Therapeutics IncAssociate Director, Clinical OperationsNewark, CA$185,000–$205,000 / yearThe 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. The base pay range for this position at commencement of employment is expected to be between $185K and $205K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Senior Staff Clinical Quality Associate (Onsite) StrykerSenior Staff Clinical Quality Associate (Onsite)Fremont, CaliforniaHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. This role provides quality and compliance oversight for clinical research activities, ensuring processes, documentation, systems, and vendor operations remain compliant, inspection-ready, and aligned with global regulatory and quality requirements.
Associate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914 Ascendis PharmaAssociate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914Palo Alto, CA$255,000–$265,000Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed.
Clinical project Associate Integrated Resources, IncClinical project AssociateFoster City, CaliforniaContractorDistributes updated study related documents (i.e. Investigative Brochures, package inserts) to study teams and internal departments as requested by the CTMA or CTM.Under close supervision reviews and participates in the quality assurance of data or documents including and not limited to GILDA and DataVision. Job DescriptionTitle: Clinical Project AssociateDuration: 06 MonthsLocation: Foster City, CAJob Responsibilities & SkillsProject involvement will be in an administrative role.
Clinical Reseach Coordinator UCSF Medical CenterClinical Reseach CoordinatorSan Francisco, CAIncumbent's 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; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist Clinical Research Manager and/or PI with oversight of other research staff; manage 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; 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. Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA 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.
Abdominal Transplant Clinical Pharmacist UCSF Medical CenterAbdominal Transplant 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.
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.
Clinical Trials Management Associate – II Integrated Resources, IncClinical Trials Management Associate – IIFoster 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 ExcelQualificationsAt least 3+ years of experience and a BS or BA in a relevant scientific disciplineFeel free to forward my email to your friends/colleagues who might be available. Job DescriptionMust 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.
Executive Director, Clinical Science, Oncology, Thoracic, Lung, Head & Neck, and Gastrointestinal Merck & Co IncExecutive Director, Clinical Science, Oncology, Thoracic, Lung, Head & Neck, and GastrointestinalSouth San Francisco, CA$255,800–$402,700 / yearRequired Skills: Advanced Analytics, Artificial Intelligence (AI), Clinical Development, Clinical Sciences, Cross-Functional Leadership, Executive Leadership, Global Clinical Studies, Innovation, Matrix Leadership, Oncology, Oncology Drug Development, Regulatory Submissions, Strategic Leadership, Talent Development. The Executive Director, Clinical Science is a senior leader within Oncology Clinical Development responsible for providing strategic, scientific, operational, and people leadership across a portfolio of oncology programs spanning multiple therapeutic areas (Thoracic, Lung, Head & Neck, and Gastrointestinal Cancers) and stages of development.
Executive Director, Clinical Science, Infectious Disease & Vaccines Merck & Co IncExecutive Director, Clinical Science, Infectious Disease & VaccinesSouth San Francisco, CA$255,800–$402,700 / yearRequired Skills: Advanced Analytics, Artificial Intelligence (AI), Clinical Development, Clinical Sciences, Cross-Functional Leadership, Drug Development, Executive Leadership, Global Clinical Studies, Infectious Disease, Innovation, Matrix Leadership, Regulatory Submissions, Strategic Leadership, Talent Development. The Executive Director, Clinical Science is a senior leader within Non-Oncology Clinical Development responsible for providing strategic, scientific, operational, and people leadership across a portfolio of infectious diseases and vaccines programs spanning multiple stages of development.
Clinical Social Worker I/II UCSF Medical CenterClinical Social Worker I/IISan Francisco, CAAssesses presenting problems, obtains psychosocial history, conducts mental status examination and diagnoses using the Diagnostic Statistical Manual (DSM-IV); participates in multi-disciplinary treatment team; act as liaison to inpatient units and other service providers to facilitate referrals and service/treatment; maintains client records according to California, City and County requirements; maintains a master-level requirements; attends staff meetings and participates in training session, other duties assigned. A Master''s degree in social work, psychology or counseling 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.
NewClinical Lab Scientist - Part Time Evenings UCSF Medical CenterClinical Lab Scientist - Part Time EveningsSan Francisco, CAUnder the direction of supervisory staff, the CLS performs routine and complex serologic testing, blood component selection, compatibility testing, transfusion reaction investigations, quality control activities, and laboratory troubleshooting to support safe and timely patient care. "Wrong unit" components include but are not restricted to: a) units other than those reserved or crossmatched for a particular patient, and b) random (stock) units when donor designated or autologous units of the component requested are available at UCSF.
Clinical 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.