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Research Associate
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Belcan Emeryville, United StatesResearch Associate · Job Number: · Category: Research Scientist · Description: Job Title: Research Associate · Pay Rate: Starting at $48 / hr depending on experience · Location: Emeryville, CA · Area Code: 510 · ZIP Code: 94608 · Start Date: Right Away · Shift: 1st shift ...
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Research Associate Iii
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Research Associate Ii
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Staff Research Associate Iii
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Research Associate I- Oakland
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Staff Research Associate 1
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Staff Research Associate 2
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Staff Research Associate 2
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Staff Research Associate 1
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University of California Berkeley Berkeley, United StatesStaff Research Associate C), QB3 Berkeley About Berkeley · At the University of California, Berkeley, we are committed to creating a community that fosters equity of experience and opportunity, and ensures that students, faculty, and staff of all backgrounds feel safe, welcome an ...
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Research Associate
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Staff Research Associate
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Research Associate
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Research Associate
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Staff Research Associate
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University of California San Francisco San Francisco, United StatesFor roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range. · **Department Description** · - The Pulmonary, Critical Care, Allergy and Sleep Medicine Program includes the UCSF Pulmonary, Critical Care, Allerg ...
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Staff Research Associate
3 weeks ago
University of California San Francisco San Francisco, United StatesFor roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range. · **Department Description** · - The Pulmonary, Critical Care, Allergy and Sleep Medicine Program includes the UCSF Pulmonary, Critical Care, Allerg ...
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Research Associate
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Actalent Redwood City, United States Full timeDescription: · Our client is seeking an RA for our Advanced Analytical team, who will work under the direction of the Team Leader to support materials analysis of our core technology platform. The ideal candidate will have relevant experience and a track record of accomplishments ...
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Research Associate
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Lawrence Berkeley Lab Emeryville, United StatesResearch Associate (Microbial and Enzyme Discovery Group) · Berkeley Lab's ( · LBNL · ) Biological Systems and Engineering ( · BSE · ) Division has an opening for a Research Associate to provide technical and research support for microbial culturing, molecular cloning, and g ...
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Research Associate
5 days ago
Lawrence Berkeley Lab Emeryville, United StatesResearch Associate (Microbial and Enzyme Discovery Group) · Berkeley Labs ( · LBNL · ) Biological Systems and Engineering ( · BSE · ) Division has an opening for a Research Associate to provide technical and research support for microbial culturing, molecular cloning, and ge ...
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Research Associate
4 hours ago
Belcan Emeryville, United StatesResearch Associate · Job Number: · Category: Research Scientist · Description: Job Title: Research Associate · Pay Rate: Starting at $48 / hr depending on experience · Location: Emeryville, CA · Area Code: 510 · ZIP Code: 94608 · Start Date: Right Away · Shift: 1st shift ...
Senior Clinical Research Associate - Emeryville, United States - Kyverna Therapeutics
Description
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases.The Kyverna therapeutic platform leverages advanced T cell engineering to suppress and eliminate autoreactive immune cells at the origin of autoimmune and inflammatory diseases.
Be at the forefront of cell therapy innovation by joining scientists, industry veterans and healthcare visionaries and help transform how autoimmune diseases are treatedKyverna is recruiting an in house Senior Clinical Research Associate (CRA) in its Clinical organization to help advance its mission to free patients from the siege of autoimmune disease.
The ideal candidate will contribute to our goals of navigating what's next in synthetic biology, immunology and cell engineering while living our core values:bring intellectual humility, elevate each other, and stay true to why. Reporting to the Sr.
Clinical Trial Manager, the Sr CRA will support the day-to-day operations of assigned Kyverna clinical trials, including start-up, conduct and close-out activities.
The Sr.CRA may, under supervision, lead the day-to-day operations of clinical trials and will also ensure the trial is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements.
The successful candidate will be a highly organized individual who can multitask and adjust direction based on changing projects and priorities.
ResponsibilitiesSupport the Clinical Trial Manager role in conduct of clinical trials.Prepare agendas for, support, and minute the internal trial team meetings.
Serve as the primary contact for selected service providers.
Ensure assigned aspects of clinical trials are managed and executed in accordance with ICH GCP, regulations, the protocol, and company-specific SOPs.
As assigned, develop study specific documents, such as template informed consent documents, study plans or manuals, case report forms, and other study level documentsAs assigned, assist in review of clinical documentation such as protocol, country- or site-specific informed consent documents, study plans or manuals, and other study level documents Participate in RFP and vendor selection process.
Participate in the identification, evaluation, selection, and oversight of clinical trial sites in collaboration with CRO.Develop and deliver study training to study staff, and internal staff on study processes.
Liaise with the CRO and study site personnel to ensure timely and correct entry of data into CRF, including the timely resolution of data queries.
Assist with reviews of data listings, data coding, patient profiles, through the study and in preparation for database lock and site close-out activities.
Maintain the Trial Master File in a state of inspection readiness.Prepare and maintain weekly internal tracking for reporting and status.
Other duties as assigned. RequirementsB.S. degree3+ years of CRA experience monitoring clinical trials in biotech, pharmaceutical, or CRO environment.
Experience with outsourced clinical trials and trial conduct from start-up through close out.
Working knowledge of relevant ICH GCP and FDA regulationsAbility to work effectively with minimal supervision.
Ability to multi-task and manage deliverables across all assigned trials.
Strong written and verbal communication skillsAbility to travel approximately 25%. Self-motivated and able to work in a small team environment.
The salary range for candidates residing in California for this position is $125,000 USD to $155,000 annually.
This salary range is an estimate of what we reasonably expect to pay for this posted position, and the actual salary may vary based on various factors, including without limitation geographic location, individual education, experience, tenure, skills and abilities, as well as internal equity and alignment with market data.
This position is also eligible for bonus, benefits, and participation in Company's stock option plan.Kyverna is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.
Kyverna is committed to the principle of equal employment opportunity for all employees and does not discriminate on the basis of race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status.
EOE/AA/Vets