- Location
- Hobart, IN · Munster, IN
- Workplace
- Onsite
- Type
- Full-time
- Department
- Operations
- Experience
- 1+ years
- Education
- High School
- Source
- Lever
Description
About Profound 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.
Own Your Studies. Grow Your Career.
If you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
What You’ll Do
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Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
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Execute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
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Lead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
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Maintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
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Track and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
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Communicate directly and professionally with investigators, sponsors, CROs, and internal teams
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Support site readiness for monitoring visits and audits
What We’re Looking For
You’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
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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
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Experience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
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Comfortable working independently and managing competing priorities
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Strong documentation skills and familiarity with EDC platforms and clinical trial management systems
