Research Associate Clinical I Jobs in Los Angeles, California

B.S. in a biology discipline (Biology, Neuroscience, Bioengineering), 0-2 years of industry experience

Experience in mammalian cell culture

Experience in DNA/RNA extraction, PCR/qPCR, ELISA, western blot, immunostaining

Effective verbal and written communication skills relating to colleagues and associates inside and outside the organization.

Maintain cell lines (hiPSCs/HEK/Glia cell) with sterile techniques.

Support and collaborate with scientists, labs, vendors, and industry experts to ensure the completion of tasks/projects.

Working knowledge of database management, personal computers, and presentation and imaging software.

Primary Job Duties and Responsibilities:

Experience in biochemistry and flow cytometry is preferred. Understanding of general research objectives.

Must possess computer skills to include, but not limited to, Excel and Word.

Performs a variety of routine laboratory tasks and procedures.

Keeps accurate and detailed project records of experiments and results.

Experience may substitute for minimum education requirements

Basic education, experience and skills required for consideration:

Preferred education experience and skills:

Conducts protocol management for an assigned set of multiple research protocols.

Performs data management and data analyses, as required by the research study.

Identifies and communicates important protocol and data management issues or problem areas to supervisor.

Participates in required training and education programs.

1-year Clinical Research Related Experience

Join our team and use your skills with an organization known nationally for excellence in research!

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.

Strong Benefits And Compensation Package

Clinical Research Associate opportunity in the oncology space!

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Working knowledge of database management, personal computers, and presentation software.

No experience is required. One to two (1 - 2) years of laboratory experience is preferred. Understanding of general research objectives.

Experience with routine laboratory procedures, experimental protocols, and overall lab organization.

Must possess computer skills to include, but not limited to, Excel and Word.

Excellent written and oral communication skills are essential.

Performs a variety of routine laboratory tasks and procedures.

Solid understanding of database management, personal computers, and presentation/imaging software.

Experience with routine laboratory procedures, experimental protocols, and overall lab organization is preferred.

May assist with animal husbandry.

Maintains lab equipment and related records.

Transports, processes and logs samples.

Maintains computer database with relevant clinical information.

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).

Participates in required training and education programs

1 year Clinical Research Related Experience preferred

Evaluates and abstracts clinical research data from source documents.

Ensures compliance with protocol and overall clinical research objectives.

Completes Case Report Forms (CRFs).

Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Experience with routine laboratory procedures and experimental protocols.

Performs routine laboratory tasks and procedures associated with banking bio-specimens.

Assists a clinical coordinator with various tasks related with bio-repository

Maintains lab equipment and related records.

Transports, processes, and logs bio-specimen samples.

Maintains computer database with relevant clinical information.

Working knowledge of database management, personal computers, and presentation and imaging software.

Must possess computer skills to include, but not limited to, Excel and Word.

Performs a variety of routine laboratory tasks and procedures.

Keeps accurate and detailed project records of experiments and results.

May assist with animal husbandry.

Maintains lab equipment and related records.

Participates in required training and education programs.

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).

Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Participates in required training and education programs.

1 year of Clinical Research Related Experience preferred

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).

Participates in required training and education programs.

Experience in a similar position is highly preferred.

Maintains the accuracy, integrity and security of complex, large computerized records systems.

Understands regulations, policies, protocols, and procedures to control and maintain accurate records.

Performs data searches and other related administrative tasks.

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

May supervise Clinical Research Associates on data entry, data query and resolution.

Participates in required training and education programs.

Must possess computer skills to include, but not limited to, Excel and Word.

Two (2) years of directly related experience preferred

Performs a variety of routine laboratory tasks and procedures.

Keeps accurate and detailed project records of experiments and results.

Working knowledge of database management, personal computers, and presentation and imaging software

Must possess computer skills to include, but not limited to, Excel and Word.

Performs a variety of routine laboratory tasks and procedures

May assist with animal husbandry

Maintains lab equipment and related records

Transports, processes and logs samples

May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.

Participates in required training and education programs.

Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution.

Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.

Coordinates research projects at an institutional or departmental level.

Communicates project status and improvement areas with leadership in a timely manner.

Maintaining broad knowledge of state-of-the-art principles and theories;

Knowledge of Microsoft Word, Excel and other Windows-based software.

Ability to simultaneously manage multiple tasks, and attention to details.

Conducting routine production of biologic product(s) including media preparation, cell culture, cell counting, formulation, centrifugation and freezing;

Compiling data for documentation of test procedures and reporting abnormalities;

Making detailed observations, planning and assisting with data collection, data analysis, writing and disseminating production results;

Working knowledge of database management, personal computers, and presentation and imaging software. Experience using Excel and Word.

May supervise Clinical Research Associates on data entry, data query and resolution.

Maintains strict research participant confidentiality according to HIPAA regulations and applicable law. Participates in required training and education programs.

Scheduling of research participants for research visits and procedures.

Maintains accurate source documents related to all research procedures.

Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.

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).