Clinical associate Jobs in Antioch ca
Last updated: 18 hours ago
- Promoted
Associate Director Clinical Development
EPM ScientificCA, United States- Promoted
CLINICAL SUPERVISOR
Sierra Health and Wellness CentersCA, United States- Promoted
Clinical Research Associate
Piper CompaniesCalifornia, CA- Promoted
- Promoted
Clinical Trial Management Associate
Hydrogen GroupCA, United States- Promoted
Associate Director / Director, Clinical Scientist
Autobahn Therapeutics, Inc.CA, United States- Promoted
Associate Director / Director of Clinical Development
GQRCA, United StatesSenior Clinical Research Associate - Oncology - West Coast
Worldwide Clinical TrialsCalifornia, USA Show moreLast updated: 30+ days ago
- Promoted
ABA Associate Clinical Supervisor
Behavior Treatment & AnalysisAntioch, California, United StatesSenior Clinical Research Associate - West Coast
BeiGeneUS, CA, Home- Promoted
Clinical Pharmacist
United States Air ForceAntioch, CA, United States- Promoted
Oncology Clinical Research Associate II
ICON Strategic SolutionsCA, United StatesAssociate Clinical Director / Adolescent Behavioral Health
Newport HealthcareOakley Show moreLast updated: 30+ days ago
- Promoted
Clinical Administrator
The Judge GroupCA, United States- Promoted
- New!
Associate Clinical Site Lead – Northern CA
AbbottCalifornia, Remote, United States- Promoted
Associate Clinical Scientist
Bayside SolutionsCA, United States- New!
Clinical Research Associate
Zachary Piper SolutionsCalifornia, CA, USSenior Associate Clinical Contracts & Budgets
ICONMARemote, CAAssociate Director Clinical Development
EPM ScientificCA, United States7 days ago
Job type
- Full-time
Job descriptionWill report to a senior member of the Clinical Development team who has direct responsibility for the overall research strategy and clinical development activities for the urticaria and stem cell programs. Will lead the design, implementation, and execution of clinical trials from Phase I-III Will participate in and / or lead cross-functional matrix team meetings including stakeholders from clinical operations, medical affairs, regulatory affairs, and biostatistics. Develop and review clinical trial protocols, informed consent documents, and other study-specific plans and essential study materials Collaborate with study team, investigators and study sites to ensure trials are conducted according to protocol, GCP guidelines, and regulatory requirements Monitor trial progress, timelines, and budgets while implementing risk mitigation strategies Responsible for clinical aspects of data review and cleaning of key studies in the urticaria and stem cell programs. Review and analyze clinical trial data, safety information, and study metrics Generate study reports, presentations, and publications to communicate findings to internal and external stakeholders Prepare and / or contribute to clinical study related and other regulatory documents (e.g. IBs, ICFs, SAPs, Data Management Plans, briefing books). Strategic Leadership Contribute to clinical development plans and product development strategies Provide scientific and medical expertise to cross-functional teams Mentor and guide clinical research associates and other team members Participate in the selection and management of CROs and vendors Support regulatory interactions and documentation preparation Cross-functional Collaboration Work closely with Clinical Operations, Biostatistics, Data Management, Medical Writing, Translational, Regulatory Affairs, Technical Operations and other functional teams to support successful execution of clinical development strategy Engage with Key Opinion Leaders and clinical investigators Lead strategy and authoring of clinical portions of regulatory submissions, responses to health authorities and ethics committees Support business development activities as needed Education and Experience Advanced degree required (MD, PhD, PharmD, or equivalent) in a relevant scientific or medical field required Minimum 5 years of clinical research experience, with at least 3 years in pharmaceutical / biotech industry Experience in immunology is strongly preferred Demonstrated experience in clinical trial design, implementation and execution with cross-functional study teams Strong understanding of drug development processes, ICH-GCP guidelines and regulatory requirements
Position Summary
- The Associate Director of Clinical Development will play a key role in planning and executing clinical trials while providing strategic input into clinical development programs. This position requires a combination of scientific expertise, project management skills, and leadership capabilities
Job Responsibilities
Qualifications