Clinical Trials Regulatory Lead
UCI
UCI in California is looking for a Regulatory Affairs Coordinator to oversee the regulatory aspects of clinical trials. Responsibilities include managing multi-phase clinical research protocols, ensuring compliance with regulatory requirements, and maintaining effective communication with various stakeholders. Candidates should have a Bachelor's degree and 3-5 years of related experience, along with strong organizational skills and the ability to work independently. Benefits offered include medical insurance and retirement savings plans. #J-18808-Ljbffr UCI
Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Clinical Trials Regulatory Lead in California, MO vacancy
$49.14 per hour
...Lead Microbiology Clinical Lab Scientist Job Category : Patient Services Requisition Number : LEADM003016 Posted : December 15... ...and participation in Quality, PI and Joint Commission and regulatory processes. Effectively manages conflict and/or change....RegulatoryHourly payFull timePioneers Memorial Healthcare District
California, MO5 days ago- ...internal controls. Ensure grant and donor reporting aligns with both international and local compliance standards. Track legal and regulatory changes across African jurisdictions and advise leadership accordingly. Conduct compliance audits/reviews to identify risks and...RegulatoryLocal area
$20.35 - $26 per hour
...responsibilities will vary depending on the hospital situation; the Shift Lead must use good judgment in prioritizing their duties on any... .... Quality check medical records, go home medications, regulatory documentations, hospital cleanliness, and timeliness of doctors...RegulatoryHourly payMinimum wageFull timeTemporary workPart timeLocal areaFlexible hoursShift workBfcareers
California, MO17 hours ago- ...Responsibilities POSITION SUMMARY The Lead Social Worker is responsible for... ...field. Experience: Two (2) year direct clinical experience in a psychiatric or mental... ...tracking tools # Monitor adherence to regulatory, accreditation and internal documentation...RegulatoryTemporary workTrial periodShift work
River Vista Behavioral Health
California, MO1 hour ago - ...|| || || --- || || || --- || **JOB DESCRIPTION** | Job Title: Lead StaffDivision/Department: ISP Group Home or Adult Residential FacilityReporting... ...open lines of communication with staff, resident, families and regulatory agencies.* Complete Special Incident Reports and complete abuse...RegulatoryTrial period
$60.51 - $66.72 per hour
...commitments, and service. Leadership, Teamwork, and Problem Solving We lead by example, acknowledging the value of our resources and using... ...shutdowns; ensures wastewater treatment plant operates within regulatory guidelines; and performs duties as assigned. Specifically, the...RegulatoryFull timeContract workShift work- The Senior Clinical Trial Manager plays a critical role in the strategic planning and execution... ...within budget, and in compliance with regulatory requirements, GCP guidelines, and... ...Essential Functions and Responsibilities Lead end-to-end execution of clinical trials...Regulatory
- ...rewards with business goals and shareholder value. You will oversee compensation strategy, equity plans, and benefits programs, ensuring governance, regulatory compliance, and market competitiveness while leading a team of professionals. #J-18808-Ljbffr Jobleads-USRegulatory
- Clinical Research Associate - Full-Service Syneos Health is a fully... ...on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good... ...completeness, reconcile it with the Trial Master File (TMF), and ensure... ...communicate out‑of‑scope activities to Lead CRA/Project Manager, and...RegulatoryInterim roleLocal areaImmediate startRemote workFlexible hours
$300k - $333k
...years of experience in product management or a related role, leading consumer or platform products or data protection initiatives.... ...or data protection. ~ Experience building data governance or regulatory compliance products in a consumer-facing context. Preferred...RegulatoryWorldwideGoogle LLC
California, MO15 hours ago- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization... ...‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good... ...contents of the ISF with the Trial Master File (TMF). Ensures...RegulatoryContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...here. Primary Function of Position The Clinical Research Associate will play a key role... ...studies to ensure compliance with all the regulatory requirements.The ideal candidate will... ...with clinical study managers, clinical trial assistants (CTAs) and data management for...RegulatoryInterim roleWork at officeLocal areaRemote workWorldwideFlexible hoursShift work
- BioPhase Solutions is seeking an experienced Clinical Trial Manager to support a growing... ...investigative sites. Key Responsibilities Lead clinical studies from start-up through... ...functionally with Clinical Operations, Regulatory, Data Management, Medical Affairs, and...Regulatory
- Description Clinical Trial Manager - Full Service Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer... ...with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions...RegulatoryContract workTemporary workImmediate startFlexible hours
- Clinical Research Coordinator (CRC) - 0-3 Years Experience Location: California, USA Job... ...data. Assist with preparation of regulatory and study documentation. Communicate with... ...project experience. Exposure to clinical trials, research protocols, or Institutional Review...RegulatoryFull timeInternshipWork at office
- ...Biostatistics will function as the statistical lead on a Jazz Pharmaceuticals drug... ...as the statistical lead for individual clinical trials, across related studies, and for integrated... ...Phase I to IV clinical studies and regulatory filings. This position may have direct...RegulatoryRemote workFlexible hours
- The Lead Clinical Research Associate (LCRA) is responsible for providing direction and leadership to the Clinical Research Associate (CRA) team and Clinical Trial Associate (CTA) assigned to studies. The LCRA ensures accurate and timely initiation, enrollment, conduct,...Contract workInterim roleRemote work
$103.6k - $176.4k
...business when needed. The MSL leads high‑value scientific... ...medical insights to support clinical research, product development... ...research and Investigator‑Initiated Trials (IITs). Deliver scientific... ...Haemonetics policies and applicable regulatory and compliance requirements;...RegulatoryHourly payTemporary workRemote workFlexible hoursHaemonetics Software Solutions
California, MO3 days ago$125k - $180k
...Clinical Scientist/Senior Clinical Scientist TenvieTherapeuticsis... ..., Translational Science, and Regulatory to ensure high‑quality clinical... ...group. JOB RESPONSIBILITIES: Lead development of core clinical... ...functional study teams for selected trials Provide clinical and...RegulatoryLocal areaRemote workTenvie Therapeutics, Inc.
California, MO2 days ago- ...The Senior Clinical Data Manager is responsible for all aspects of... ...through database lock of clinical trials. The Sr/CDM has a broad,... ...coordinating and performing UAT. Leads the development of the... ...clinical trials process, and regulatory requirements. Good working knowledge...RegulatoryFor contractors
Bayside Solutions
California, MO2 days ago - Clinical Trial Manager - Oncology - Remote in California Elixir Associates are pleased to be... ...as the company scales. About The Job: Lead and oversee Oncology clinical trial execution... ..., ICH/GCP guidelines, and applicable regulatory requirements, collaborating closely...RegulatoryRemote work
- Lead all clinical study operations, providing strategic/tactical planning, organization, and direction... ...in compliance with GCP, relevant SOPs, regulatory requirements, and project-specific... ...Clinical Project Management, Clinical Trial Operations, Study Planning, Study Start...Regulatory
- ...expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies, and sound knowledge of applicable... ...internal cross-functional teams (engineering, product development, regulatory, post-market surveillance) to define and plan the strategy...RegulatoryLocal areaWorldwideFlexible hours
Intuitive
California, MO3 days ago - Overview Business Development Director for Clinical Trial Supply, USA Salary: Dependent on... ...supply chain, and quality stakeholders Lead RFI/RFP responses, commercial proposals... ...market trends, competitor offerings and regulatory developments impacting clinical supply...RegulatoryRemote work
- ...through education, training, research and clinical care. Your Role on the Team The... ...both the outpatient clinic and clinical trials. The Clinical Psychologist will work amongst... ...skills. Ability to negotiate multilayered regulatory systems and manage competing priorities,...RegulatoryTraineeshipLocal area
UC Irvine
California, MO4 days ago - ...redesign tools. Microsoft Office Suite applications, including Outlook, Word, Excel, Access, Visio, and PowerPoint. Managed healthcare regulatory requirements. Supervisory principles and practices, as well as techniques and methods to organize and manage direct reports....RegulatoryFull timeWork at office
- ...FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois &... ...of ICH GCP, and international and local regulatory requirements Passion for clinical... ...primarily responsible for monitoring clinical trials and Ensuring that clinical trial is...RegulatoryPart timeFreelanceLocal areaRemote work
$137.5k - $220.1k
...Job Description The Manager, Clinical Operations (Specimen Management... ...serves as the overall team lead for multiple studies of high... ...s). Provide oversight of the Trial Master File (TMF) activities... ...clinical research guidelines and regulatory requirements. Must have hands...RegulatoryHourly payDaily paidContract workTemporary workWork at officeLocal areaImmediate startRemote workFlexible hoursShift work$93.6k - $114.4k
Clinical Trial Assistant W2 Contract-to-Hire Salary Range: $93,600 - $114,400 per year Location: Redwood City, CA - Hybrid Role Base... ...functional visibility. Support development and maintenance of RCR (Regulatory Compliance Review) packs for Phase I Healthy Volunteer...RegulatoryContract work$85k - $175k
...Manager to provide independent oversight of clinical trial activities, processes, and... ...role focuses on ensuring compliance with regulatory requirements, internal procedures, and... ...Assurance plans aligned with GCP standards Lead and support audit and inspection readiness...RegulatoryFull timeWork at officeLocal area
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Trials Regulatory Lead. Be the first to apply!
Related searches
- regulatory accountant California, MO
- regulatory law California, MO
- regulatory California, MO
- regulatory contract California, MO
- clinical research regulatory California, MO
- regulatory scientist California, MO
- regulatory engineer California, MO
- food regulatory California, MO
- regulatory technician California, MO
- regulatory executive California, MO