Clinical associate jobs in Tulare, CA

Clinical Research Associate 6 month contract Onsite in San Diego, CA Responsibilities. Carry out.. Apply knowledge of FDA regulations to site monitoring and clinical study design duties. Monitor and..

Associate Clinical Scientist W2 Contract Salary Range. 83,200. 104,000 per year Location. Redwood City.. Hybrid Role Job Summary. As an Associate Clinical Scientist, you will work with cross functional teams..

They are seeking a seasoned Clinical Research Associate to join their growing team. As a Clinical.. Responsibilities. Study Management. Assist in the design and implementation of clinical study protocols..

Job Summary. The Clinical Research Associate will provide support to the Senior Director, Clinical.. This position will play a key role in contributing to the oversight of the clinical monitoring function..

At least 5 years of clinical trial management experience, preferably in the medical device industry.. Strong knowledge of clinical research regulations (ICH GCP, ISO 14155, FDA, and EU). Proven success in..

THE COMPANY 89bio is a clinical stage biopharmaceutical company focused on the development and.. The functional role of the Senior Manager Associate Director, Clinical Sciences is that of a Senior..

Job Title. AD Director of Clinical Development Location. South San Francisco (Hybrid. 3 days onsite.. VP of Clinical Development Overview. The AD Director of Clinical Development will oversee the execution..

Div. br. div. div class "olUlHelper pl10px". TRUE JOB TITLE. Vendor Qualification Associate I. br. br.. The candidate should also have an understanding of various clinical trial activities such as clinical..

When our values align, there's no limit to what we can achieve. Our clinical operating model drives.. As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of..

Oncology Early Stage Clinical Scientists Hybrid. Bay Area, CA 6 Month Initial Contract Position We are.. Working closely with other functional disciplines, including Clinical Operations, Biostatistics Data..

Position Title. Clinical Psychologist Location. Clarity Psychological Testing, California (Remote.. The Clinical Psychologist will be responsible for interpreting test results and providing detailed..

Other duties as assigned. The ideal candidate will have. Registered Nurse Credential 5. years OPO clinical experience 2. years leadership experience Valid Drivers License with ability to pass..

Our partner, a global manufacturer of specialty medical products, is looking to add a Clinical.. In this role, you would provide advanced clinical and technical support for physicians and support staff..

As Sr. Associate, Clinical Contracts & Budgets, you will provide clinical site contracting services to.. Responsibilities. Manage end to end process for clinical site contracts and clinical trial related..

Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and.. Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory..

Senior Associate Clinical Contracts & Budgets Location. RemoteDuration. months with possible extension.. AccountabilitiesProvide clinical site contracting services to clinical study teams to support study..

The OpportunityThe Associate Clinical Site Lead for the Northern California region drives study.. Monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and..

The Opportunity. Total Life is currently seeking a dynamic and enthusiastic. Associate Clinical Social.. in the state of. California. who is looking to fill their clinical hours for licensure. by providing..

Position Summary. The Senior Clinical Trial Manager will play a key role in the planning, coordination.. The Senior Clinical Trial Manager will ensure that clinical trials are conducted on time, within budget..

Manage CROs and other clinical vendors to ensure that project and corporate goals are achieved on time.. Lead the development and review of key clinical documents, including protocols, informed consent forms..