Clinical Research Assistant at Indiana Medical Research Institute LLC
Merrillville, IN 46410, USA -
Full Time


Start Date

Immediate

Expiry Date

14 Nov, 25

Salary

19.0

Posted On

15 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Life Sciences, Health Insurance, Microsoft Office, R, Python, Vision Insurance, Sas, Biology, Biochemistry, Dental Insurance, Time Management

Industry

Pharmaceuticals

Description

POSITION SUMMARY

Indiana Medical Research Institute LLC is seeking a proactive and detail-oriented Research Assistant to support the daily operations of clinical trials. This is a unique opportunity to contribute to the advancement of medical therapies in a collaborative, mission-driven environment. The ideal candidate demonstrates scientific curiosity, strong organizational skills, and a commitment to high-quality, compliant research practices.

QUALIFICATIONS

  • Bachelor’s degree in Biology, Life Sciences, Biochemistry, or related field.
  • Prior experience in clinical or biomedical research, or laboratory work (preferred).
  • Solid understanding of molecular and cellular biology concepts.
  • Familiarity with FDA regulations and ICH-GCP standards.
  • Proficient in Microsoft Office; experience with data analysis tools (SAS, R, Python) is a plus.
  • Excellent written/verbal communication, time management, and organizational skills.
  • Strong attention to detail and commitment to data accuracy and integrity.
    Job Type: Full-time
    Pay: $18.00 - $19.00 per hour

Benefits:

  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Work Location: In perso

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities
  • Assist in planning, coordinating, and executing clinical studies in accordance with approved protocols.
  • Collect, analyze, and interpret clinical and experimental data with accuracy and precision.
  • Maintain organized research records, logs, and documentation for audits and regulatory reporting.
  • Collaborate with research coordinators and investigators to prepare study reports, charts, and presentations.
  • Support laboratory activities, including tissue and cell culture, assays, and proper specimen handling.
  • Ensure all activities comply with FDA regulations, GCP guidelines, and internal SOPs.
  • Prepare study materials and assist in coordinating participant visits as needed.
Loading...