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Clinical Operations Lead
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Clinical Operations Associate Director
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Clinical Operations Associate Director
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Contact Center Team Lead
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Practice Coordinator 3
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Clinical Operations Intern
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Clinic Operations Manager
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Kaiser Oakland, United States Full timeQualified external candidates may be eligible for Sign-On Bonus · Job Summary: · Promotes professional development through the application of principles of adult learning in broad-based program development. Leveraging expertise in Kaiser Permanentes electronic medical record, KP ...
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Clinical Operations Manager
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Mochi Health San Francisco, United StatesIn a world where healthcare can feel like a maze of bureaucracy and frustration, Mochi Health offers a refreshing oasis. We're not just another telehealth clinic - we're on a mission to rewrite the script on healthcare, starting with the most overlooked areas of medicine. With a ...
Associate Director, Clinical Operations - Emeryville, United States - Kyverna Therapeutics, Inc.
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 treatedThe Associate Director, Clinical Operations will manage clinical trials in coordination with a clinical operations team. This individual will be involved in the daily operations of Kyverna's clinical programs through vendors.
This person may lead a team of clinical operations professionals and will be expected to provide vision, leadership, and mentoring to their assigned team.
He or she must have an expert and comprehensive understanding of ICH/GCP requirements, principles, concepts, industry practices, and standards.Under the direction of a senior clinical operations person, this individual is responsible for clinical trial management through CROs, oversight and successful execution of Kyverna's clinical trials according to regulatory guidelines.
He or she must facilitate effective internal and external relationships.This person is also responsible for the achievement of project goals and objectives on time and on budget.
The position will have some travel requirements. The candidate will be expected to contribute to Investigator Meetings, site relationships and vendor management which may include face-to-face interaction
Responsibilities
Manage complex Phase 1, 2, 3, and 4 clinical trials as part of a small operational team
Demonstrate oversight of vendors and work in a quality framework that supports early and late development work
Responsible for vendor management activities including attendance and input at team meetings and tracking and follow up on action items.
Lead study start up process and cross functional planning in support of study start upProvide review and input on clinical documents (protocols, informed consent documents, monitoring plans, clinical trials report, investigator brochures, etc.)
Conduct feasibility and site selection
Coordinate closely with Clinical Development, Biostatistics, Data Management, Drug Safety, Legal, Finance, Project Management and Regulatory to ensure operational excellence.
Prepare clinical research budgets and timelinesAnalyze and develop action plans to address issues with investigational sites, CRAs, and CROs
Requirements
Strong knowledge in the areas of drug development, operations, and strategic planning, specifically management of clinical trial operations
Demonstrated experience in study start up and vendor oversight
Experience with rare disease clinical trials a plus
Demonstrated knowledge of international clinical pharmaceutical standards, ICH/GCP guidelines, and regulatory compliance
International experience is highly preferred
Must have experience managing CROs, central laboratories, and other clinical study vendors
Must have a working knowledge of data management, data review and analysis, and drug safety and Pharmacovigilance
Ability to work on and solve complex problems
Ability to prioritize and handle multiple tasks simultaneously
Excellent communication/interaction skills and experience in a dynamic, small organization
$185,000 - $210,000 a year
The salary range for candidates residing in California for this position is $185,000 USD to $210,000 USD 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.
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