Profound Research
Contractor- Clinical Research Coordinator (Detroit, MI)
Detroit, MI · Contract
Sponsorship not specifiedDetected 50 days ago
GCPComplianceClinical TrialsClinical ResearchResearchLeadershipCommunicationGxP
About the role
- We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care.
- Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship.
- Why This Role Exists If you're ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
Responsibilities
- Lead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
- Maintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
- Track, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
- Support site readiness for monitoring visits, sponsor communications, internal quality review, and audits
- Follow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
- Help maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
- We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency.
- We actively support internal growth and create pathways for people to take on greater responsibility over time
- Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that's rare in a single organization
Requirements
- You have clinical research experience and are ready to operate with more ownership.
- Bachelor's degree with 1+ year of relevant experience, OR Associate's degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
- Prior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
- Experience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
- Familiarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
- Working knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
- Strong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
- You'll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams.
- This is not an entry-level support role - you'll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
Nice to have
- Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
- Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
- May be required to wear personal protective equipment (PPE) in accordance with facility protocols
- Experience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
- Experience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
- Active or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
- Experience supporting start-up, closeout, or audit/monitoring readiness activities
- Comfort adapting quickly to study-specific workflows, systems, and enrollment timelines
Compensation
- Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
Benefits
- Competitive compensation, health insurance, PTO, retirement plan, and professional development support
- We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
Company info
- Improving Lives by Providing Advanced Therapeutic Options
- Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research
- Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered.
- Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.
- Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency.
- Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.
- Why This Role Exists
- If you're ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
- As a Clinical Research Coordinator I at Profound Research, you'll support the execution of high-volume vaccine clinical trials at one of our sites.
- This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability.
- If you're looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we'd like to hear from you.
- You'll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
Visa & Work Authorization
- Support site readiness for monitoring visits, sponsor communications, internal quality review, and audits
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This listing is sourced directly from Profound Research's careers page and normalized into a canonical job model.