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Clinical Research Assistant

Job in Columbus, Franklin County, Ohio, 43224, USA
Listing for: SQRL
Full Time, Seasonal/Temporary position
Listed on 2026-01-01
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Assistant/Associate
Salary/Wage Range or Industry Benchmark: 40000 - 45000 USD Yearly USD 40000.00 45000.00 YEAR
Job Description & How to Apply Below

Overview

Associate Director of Recruiting at SQRL | Clinical Research, Healthcare, Biotech, Life Sciences

Highlights

  • $40,000 - $45,000 salary + benefits!
  • Unique opportunity to break into the Clinical Research space!
  • Work with a company that truly cares about their employees and patients
  • Consistent schedule, no overnights or weekends, Early Fridays, flex holidays, and more!

We can only consider local candidates at this time, no relocation candidates

About Our Client

Our client is a long standing clinical research site in the Columbus, OH area that takes a truly unique patient-centric, service-oriented approach to clinical research. Their reputation for excellence has been built across over 20 therapeutic areas, over 15 physicians, and hundreds completed trials. They are looking to expand their team with additional clinical research assistants; also providing the exciting opportunity to train and develop into CRCs over time!

Job Description

As a Clinical Research Assistant, you will play a crucial role in supporting clinical research activities. You will work closely with study team members under the direct supervision of a research manager and support other study team members to achieve study objectives and company goals. Compassion, patient focused mindset, and collaboration are all important traits!

Responsibilities
  • Develop strong working relationships with team members and office staff to build a foundation of trust and respect
  • Assist with the screening, recruiting and enrollment of research patients
  • Data entry and Management
  • Coordinate follow-up care and laboratory procedures
  • Adhere to an IRB approved protocol
  • Assist in the informed consent process of research subjects
  • Support the safety of research subjects
  • Coordinate protocol related research procedures, study visits, and follow-up care
  • Schedule subject visits and procedures
  • Work with various clinical research software
Qualifications
  • 1+ year experience in communication skills from a medical, patient facing setting
  • Ability to work on site Monday - Friday in Columbus, OH
  • Ability to or Willingness to learn blood draws, scans, EKG, patient education, etc
Employment Details
  • Seniority level
    :
    Associate
  • Employment type
    :
    Full-time
  • Job function
    :
    Research
  • Industries
    :
    Research Services
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