Clinical Research Coordinator - Southfield, MI
IQVIA · Southfield, MI · Global
Clinical Research
–
Not yet analysed
Demand68
Career growth62
Healthcare fit72
Remote potential15
5-year outlook
CRC pay is typically modest at entry and rises with GCP experience, therapeutic-area breadth, and progression into CRA, site lead, or sponsor-side clinical operations roles; IQVIA's CRO scale can open internal mobility. Exact figures vary by market and are not stated in the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
unclear
Employment type
–
Date found
2026-10-20
Intelligence details
Why this is worth applying to
Worth considering if you want a structured entry point into industry-sponsored clinical research and are willing to work on-site; confirm the experience and any phlebotomy/licensure requirements before investing time, since the posting text is empty.
Who should apply
IMGs and healthcare graduates seeking a first industry-adjacent research role; nurses or allied health staff with patient-facing trial exposure; pharmacists or life-science graduates with GCP familiarity; anyone in the Detroit metro area able to commute to Southfield.
CV angle
Reframe real clinical experience into trial-operations language: patient screening and eligibility assessment, informed consent discussions, protocol-driven documentation, adverse event recognition and escalation, multidisciplinary coordination, and audit-ready record keeping. Name any exposure to EDC/eCRF systems, IRB or ethics submissions, or research audits, and state GCP training status explicitly — do not claim coordination experience you do not have.
Skills to highlight
- Informed consent and participant communication
- Protocol adherence and eligibility screening
- Source documentation and data accuracy
- Adverse event identification and reporting
- IRB/ethics and regulatory documentation
- Multidisciplinary team coordination
- Attention to detail in audit-ready records
- Participant recruitment and retention
Role summary
Site-level coordination of industry clinical trials: screening and consenting participants, running study visits per protocol, completing source documents and eCRFs, maintaining regulatory binders, and liaising with sponsors, monitors, and IRBs. Predominantly on-site at a research site or investigator office.
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