Clinical Research Representative

  • location: Santa Ana, CA
  • type: Contract
  • salary: $30 - $34.58 per hour
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job description

Clinical Research Representative

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: Santa Ana, California
job type: Contract
salary: $30.00 - 34.58 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • As a Clinical Research Representative you are a detail-oriented, agile and high performing individual who will be responsible for managing and ensuring accuracy of study documents and materials in a fast-paced, complex environment.
  • Review and ensure accuracy and completeness of clinical study files
  • Organize documents and data in Veeva/eTMF (electronic trial master file), CTMS (clinical trial management system) and ensure compliance with internal procedures. May review clinical data for completeness for multiple clinical research trials
  • Collate new study materials, create study binders, patient recruitment materials, and arrange shipment of materials to clinical sites
  • Tracking/management of internal training files
  • Additional incidental duties assigned by leadership
 
qualifications:
  • A bachelor's degree preferred, related field preferred.
  • 1 year of previous clinical research experience and medical device or regulated industry preferred.
  • Experience with Clinical Systems such as Veeva/eTMF (electronic Trial Master File) and CTMS (Clinical Trial Management System) preferred.
  • Key responsibilities:
  • Review and ensure accuracy and completeness of clinical study files
  • Organize documents and data in Veeva/eTMF (electronic trial master file), CTMS (clinical trial management system) and ensure compliance with internal procedures. May review clinical data for completeness for multiple clinical research trials
  • Collate new study materials, create study binders, patient recruitment materials, and arrange shipment of materials to clinical sites
  • Tracking/management of internal training files
  • Additional incidental duties assigned by leadership
 
skills: CTMS (Clinical Trial Management Systems), TMF
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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