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Remote Clinical Research Associate Jobs in California

Clinical Research Associate Jobs
By Infosoft, Inc. At Irvine, CA, United States
Solid understanding and knowledge of principles, theories, and concepts relevant to clinical trial management
3 years of previous hands-onclinical researchexperience
Good computer skills in usage of MS Office Suite including MS Project and excellent Excel skills required
Excellent written and verbal communication skills and interpersonal relationship skills
Solid knowledge of human anatomy and physiology
Good problem-solving, organizational, analytical, and critical thinking skills
Clinical Research Associate Jobs
By BioPhase At San Diego Metropolitan Area, United States
Conduct study site selection, qualification, training, start up, and close out .
Assist with data entry as necessary.
-A minimum of 2 years' direct experience in clinical study monitoring is required.
-Experience in IVD studies is preferred, with a proven track record of progressive clinical study responsibility.
-Knowledge of medical terminology and good clinical practice required.
Detail-oriented with a high level of organizational skills.
Clinical Research Associate Jobs
By Ansun BioPharma Inc At , San Diego, 92121, Ca $75,000 - $95,000 a year
Qualification / Education/ Experiences/ Skills
Late-stage clinical trial experience and working knowledge of US regulatory agency requirements, preferred
Conduct medical monitoring, pharmacovigilance, regulatory, data management related to delegated clinical study.
Manage investigational product (IP) accountability and reconciliation process
Minimum BA/BS in scientific, life science, or related field with 2+ years CRA related experiences
Sponsor-side clinical trial experience in the pharmaceutical industry is preferred
Research Associate - Remote | Wfh
By Get It Recruit - Information Technology At Oakland, CA, United States

Are you passionate about addressing climate change and promoting equity? We are seeking a dedicated and experienced Researcher to join our dynamic team. As a Researcher at our organization, you will ...

Cra (Clinical Research Associate)
By Agilent Technologies At Santa Clara, CA, United States
Assist with site audits and site quality management activities, as needed.
Please update the minimum qualifications below to reflect the requirements for your specific role.
Ensure monitoring activities (remote and on-site) are completed in accordance with Agilent procedures and study monitoring plan.
Assures adherence to GCP, study protocol, and all applicable requirements through routine monitoring visits.
3+ years direct clinical research experience at a sponsor or CRO as a CRA/study monitor, or equivalent experience.
Diagnostic/IVD experience highly preferred, oncology or other medical device experience is also accepted.
Clinical Research Associate Jobs
By Rangam At Alameda County, CA, United States
Bachelor’s degree REUIRED WITH A PREFERANCE IN Biological Sciences which fit best BUT “Life Sciences” degrees will also be considered
Minimum of 3 to 5 years of clinical exp. within industry
Specifically looking for monitoring exp. on the sponsor side
Will be supporting a multi-site study
Will be doing monitoring visits
Medical device exp. of at least 1 year
Clinical Research Associate Jobs
By Intellectt Inc At Alameda, CA, United States
• Minimum of 3 to 5 years of clinical exp. within industry
• Specifically looking for monitoring exp. on the sponsor side
• Will be supporting a multi-site study
• Exp. with site selection
• Will be doing monitoring visits
• Medical device exp. of at least 1 year
Clinical Research Associate I
By Nevro At Redwood City, CA, United States
2 years of related experience in supporting medical device clinical trials
Strong interpersonal and communication skills
Able to manage multiple tasks
Experience working directly with US and EU sites strongly desired
Experience working with clinical data and databases (desirable)
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
Clinical Research Coordinator - Hybrid/Remote - 122856
By UC San Diego Health At San Diego, CA, United States
Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
Strong knowledge of investigational protocols especially with pediatric protocols (data management, query resolution, protocol design, protocol writing and protocol implementation).
Demonstrated experience in clinical trials research. Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
Demonstrated experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Staff Research Associate - Hybrid/Remote - 122722
By UC San Diego Health At San Diego, CA, United States
Knowledge of tissue culture and experience with maintenance of tissue culture facility.
Knowledge & experience of proper handling, storage, and disposal of hazardous chemicals and biohazardous materials.
Experience of basic laboratory procedures and equipment, including preparation of buffers, solutions and reagents and sterile techniques.
Experience with hiPSCs and organoid differentiation.
Background and demonstrated familiarity with Molecular Biology (CRISPR genome editing) and/or Mammalian Tissue Culture (human stem cells).
Natural tendency to create order, organize, and attention to detail.
Clinical Project Manager/Sr. Clinical Research Associate
By TalentZök At Carlsbad, CA, United States
3-5 years clinical study management experience
Minimum: 5 years clinical study management experience
Manage clinical operations for post-market observational registry at study sites in the US
Manage sites by tracking regulatory submissions/approvals, patient recruitment, case report form completion and data queries.
Administer electronic data capture (EDC) system for data entry by study site staff.
Manage invoices from contracted study sites and vendors.
Clinical Research Associate Ii
By Labcorp At , San Diego, 92128, Ca $90,000 - $125,000 a year
Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements
Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process
Good planning, organization and problem-solving abilities; Ability to work with minimal supervision
Organize and make presentations at Investigator Meetings
Participate in the development of protocols and Case Report Forms as assigned
Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
Clinical Research Associate I
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1 year Clinical Research Related Experience
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Clinical Research Associate I - Regenerative Medicine Institute
By CEDARS-SINAI At , Los Angeles, Ca $17.57 - $29.87 an hour
Participates in required training and education programs.
Understanding of general clinical research objectives. One (1) year of clinical research experience is preferred.
Ability to interpret and apply knowledge of State, Federal and Agency standards to comply with regulations.
Must possess computer skills, including Word and Excel, and the ability to use standard office equipment is required.
Assists with clinical trial budgets and patient research billing.
Completes Case Report Forms (CRFs).
Clinical Research Associate Jobs
By FibroGen, Inc. At , San Francisco, 94158, Ca $98,000 - $113,100 a year
Manages submission of documents and maintenance of the Trial Master File (TMF); reviews TMF to ensure inspection-readiness
At least 2 years of relevant experience in the pharmaceutical industry, Biotech or equivalent
Knowledge of GCP and ICH guidelines required
Excellent communication and interpersonal skills
Strong computer skills in MS Word, Excel, Outlook, and PowerPoint
Responsible for ensuring external service providers execute activities in a quality manner and per the established contract

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and