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Day Shift Irb Jobs in Indiana (NOW HIRING)

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Day Shift Irb information

What is the difference between Day Shift Irb vs Day Shift Clinical Research Coordinator?

AspectDay Shift IrbDay Shift Clinical Research Coordinator
CertificationsIRB approval, research compliance trainingGood Clinical Practice (GCP), research ethics
Work EnvironmentReviewing protocols, ensuring compliance, office settingParticipant interaction, site management, office/lab setting
Employer & IndustryHospitals, research institutions, biotech firmsHospitals, research centers, pharmaceutical companies

Both roles involve research oversight and require knowledge of clinical protocols. The Day Shift Irb primarily focuses on reviewing and approving research protocols to ensure ethical standards, while the Day Shift Clinical Research Coordinator manages participant recruitment, data collection, and study coordination. Understanding these differences helps candidates choose the role that best fits their skills and career goals.

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Clinical Research Coordinator

ECN Operating LLC

Merrillville, IN • On-site

$23.75 - $31.75/hr

Full-time

Posted 12 days ago

Job description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

  • Coordinate day-to-day clinical research activities to ensure study protocols are followed.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent and ensure ethical conduct in all study interactions.
  • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
  • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
  • Maintain accurate and timely documentation in case report forms and electronic databases.
  • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
  • Schedule participant visits and follow-ups; ensure visit windows are met.
  • Ensure proper storage, handling, and accountability of investigational products, if applicable.
  • Maintain regulatory documents and assist with IRB submissions.

Qualifications:

  • Bachelor's degree in a health-related field required.
  • At least 1–2 years of experience in clinical research preferred.
  • Phlebotomy certification or MA certification preferred.
  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and communication skills.
  • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

  • Experience working in clinical trials, especially in a hospital or academic setting.
  • Familiarity with IRB processes and clinical trial documentation.
  • Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

  • 8 hour shift
  • Monday to Friday
  • Weekends as needed

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