Associate Clinical Operation Manager

JAC Recruitment

120K–170K a year

Behavioral Health Market Context

Apply Nowvia Talents By Vaia

Benefits

Health InsuranceDental Coverage

Job Description

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Our client- Pharmaceutical company – is looking for Associate Clinical Operation Manager.

This position needs to report to Elk Grove Village IL office hybrid (2-3 times a week)

Responsibilities
• Support clinical trial start-up, execution, and close-out activities in the U.S.
• Assist with site feasibility, selection, initiation, and communication with site staff.
• Ensure adherence to FDA regulations, ICH-GCP, and internal SOPs across clinical operations.
• Coordinate with CROs and vendors to track study timelines, deliverables, and issue resolution.
• Help maintain and organize clinical documentation, including TMF and site-level records.
• Assist in implementation and maintenance of systems such as CTMS, eTMF, and issue tracking logs.
• Other task might include

Requirements
• Bachelor’s degree in Life Sciences, Nursing, or a related field
• 2–4 years of experience in clinical operations or trial coordination
• Basic understanding of FDA regulations, ICH-GCP, and clinical trial workflows
• Experience with clinical documentation systems (eTMF, CTMS)
• Exposure to vendor or CRO collaboration
• Ability to follow procedures and escalate issues appropriately
• Project management awareness
• Proficiency in Microsoft Office and document management tools

SALARY

USD $ 120,000 - 170,000

Benefits

Medical Dental Vision 401K and others.

#countryUS

Seniority level
• Seniority level
Entry level
Employment type
• Employment type
Full-time
Job function
• Job function
Management and Manufacturing
• Industries
Staffing and Recruiting

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Salary: USD 120000 - 170000 per year

Experience: 3 years required

Qualifications

  • Bachelor’s degree in Life Sciences, Nursing, or a related field
  • 2–4 years of experience in clinical operations or trial coordination
  • Basic understanding of FDA regulations, ICH-GCP, and clinical trial workflows
  • Experience with clinical documentation systems (eTMF, CTMS)
  • Exposure to vendor or CRO collaboration
  • Ability to follow procedures and escalate issues appropriately
  • Project management awareness
  • Proficiency in Microsoft Office and document management tools
  • Quality Assurance Manager, RWE Clinical Trials (Remote)
  • Streeterville, IL $83,200.00-$137,280.00 5 days ago
  • Scientific Manager, COA Implementation, Patient Centered Solutions
  • Streeterville, IL $89,440.00-$147,576.00 1 month ago
  • Chicago, IL $110,000.00-$115,000.00 2 months ago
  • Experience: 3 years required

Benefits

  • USD $ 120,000 - 170,000
  • Medical Dental Vision 401K and others
  • Salary: USD 120000 - 170000 per year

Responsibilities

  • This position needs to report to Elk Grove Village IL office hybrid (2-3 times a week)
  • Support clinical trial start-up, execution, and close-out activities in the U.S
  • Assist with site feasibility, selection, initiation, and communication with site staff
  • Ensure adherence to FDA regulations, ICH-GCP, and internal SOPs across clinical operations
  • Coordinate with CROs and vendors to track study timelines, deliverables, and issue resolution
  • Help maintain and organize clinical documentation, including TMF and site-level records
  • Assist in implementation and maintenance of systems such as CTMS, eTMF, and issue tracking logs
  • Other task might include
  • Nonclinical Development Manager/ Sr


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