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Clinical Research Coordinator

SGA Inc.

Kalamazoo, MI

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JOB DETAILS
SALARY
$30–$38 Per Hour
SKILLS
Case Report Form (CRF), Clinical Competency, Clinical Research, Clinical Study Publications, Clinical Trial, Communication Skills, Consulting, Contract Management, Customer Support/Service, Data Collection, Data Entry, Documentation, GCP (Good Clinical Practices), Healthcare, Healthcare Administration, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Interpersonal Skills, Maintain Compliance, Oncology, Organizational Skills, Patient Administration, Patient Follow-up, Presentation/Verbal Skills, Regulations, Regulatory Compliance, Regulatory Submissions, Society of Clinical Research Associates (SoCRA), Staff Development, Time Management, Writing Skills
LOCATION
Kalamazoo, MI
POSTED
4 days ago
Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Research Coordinator for a Contract to hire assignment with one of our premier Healthcare clients in Kalamazoo, MI.

Responsibilities :
  • Prepare, submit, and monitor documentation for research programs.
  • Ensure compliance with research regulations and protocols through audits.
  • Advise caregivers on program design, treatment administration, and patient follow-up.
  • Organize study files, including regulatory binders and source documentation.
  • Maintain and update study files and records according to sponsor and institutional requirements.
  • Review, edit, and update informed consent documents for clinical trials.
  • Collaborate with the Principal Investigator (PI) to prepare IRB and regulatory submissions.
  • Assist in reviewing eligibility criteria for participant enrollment.
  • Coordinate enrollment of participants into Children's Oncology Group (COG) studies.
  • Develop familiarity with COG protocols and specimen submission guidelines.
  • Collect study data and ensure timely completion of Case Report Forms.
  • Coordinate audits with the central COG office and maintain audit readiness.
  • Perform additional duties as assigned.
Required Skills:
  • Must have previous experience with COG - 5 years
  • Bachelor's degree in a scientific or healthcare field, or equivalent experience in Data entry, Research, Healthcare administration education in the protection of human research participants and Good Clinical Practices required.
  • Current clinical licensure and board certifications:
    SOCRA (preferred)
    ACRP (preferred within 4 years of hire)
    CITI training
    Human protections training
    IATA certification for shipping infectious substances and diagnostic specimens.
  • Ability to read and interpret:
    Research documents
    Clinical trial documents
    Operating and maintenance instructions
    Procedure manuals
  • Strong written and verbal communication skills.
  • Excellent interpersonal and relationship-building skills


SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at https://sgainc.com/ .

SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company EEO page to request an accommodation or assistance regarding our policy.Salary:30-38 USD/Hour

About the Company

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SGA Inc.

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