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Randstad Research Assistant in Huntington Beach, California

Research Assistant

job details:

  • location:Huntington Beach, CA

  • salary:$30.47 - $35.85 per hour

  • date posted:Thursday, June 17, 2021

  • experience:3 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:36954

job description

Research Assistant

job summary:

As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: Huntington Beach, California

job type: Contract

salary: $30.47 - 35.85 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

Responsibilites:

A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.

  • Verify and/or correct research study information on source documents. Research queries and variances, and provide feedback to the site data collector

  • Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness

  • Prepare and maintain research study files

  • Compile, collate and submit study information within established deadlines

  • Assist in maintenance of regulatory documentation

  • Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits

  • Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget

  • Processing of required lab specimens, labeling of vials, and accurately filling out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations

  • Perform various administrative support functions such as reception, office organization, and office supply management

qualifications:

Education & Qualifications:

  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting; e.g. clinical research coordinator, nurse, medical assistant

  • Basic knowledge of clinical trials

  • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

  • Basic knowledge of medical terminology

  • Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

  • Excellent interpersonal skills

skills: GCP (Good Clinical Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

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