... nurses, and research staff to maintain compliance and accurate documentation. * Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems. * Build ...
... nurses, and research staff to maintain compliance and accurate documentation. * Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems. * Build ...
... nurses, and research staff to maintain compliance and accurate documentation. * Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems. * Build ...
... nurses, and research staff to maintain compliance and accurate documentation. * Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems. * Build ...
Clinical Research Coordinator I -RN
New Albany, IN · On-site
$63K - $80K/yr
A Clinical Research Coordinator I - RN at Iterative Health is an essential member of the site ... Experience with CTMS, EDC, or eTMF platforms. * ACRP or SOCRA certification (CCRC or CCRP), or ...
Clinical Research Coordinator I -RN
New Albany, IN · On-site
$63K - $80K/yr
A Clinical Research Coordinator I - RN at Iterative Health is an essential member of the site ... Experience with CTMS, EDC, or eTMF platforms. * ACRP or SOCRA certification (CCRC or CCRP), or ...
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Clinical Research Assistant II
Evansville, IN · On-site
Enter study data into sponsor electronic data capture (EDC) systems and internal databases ... Certified Medical Assistant (CMA), Registered Medical Assistant (RMA), Licensed Practical Nurse ...
Quick apply
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Clinical Research Assistant II
Evansville, IN · On-site
Enter study data into sponsor electronic data capture (EDC) systems and internal databases ... Certified Medical Assistant (CMA), Registered Medical Assistant (RMA), Licensed Practical Nurse ...
Edc Nurse information
What is the difference between Edc Nurse vs Clinical Research Nurse?
| Aspect | Edc Nurse | Clinical Research Nurse |
|---|---|---|
| Certifications | RN license, EDC-specific training | RN license, research certifications often preferred |
| Work Environment | Clinical settings, hospitals, research sites | Research facilities, hospitals, clinical trial sites |
| Employer & Industry | Pharmaceutical companies, research organizations | Academic institutions, hospitals, research organizations |
| Primary Focus | Data entry, electronic data capture (EDC) systems | Patient care, protocol adherence, data collection |
While both roles involve clinical settings and require nursing credentials, Edc Nurses specialize in electronic data capture and management within research studies, focusing on data accuracy and system use. Clinical Research Nurses have a broader role in patient care and protocol management during clinical trials. Understanding these differences helps in choosing the right career path or job opportunity.
Job description
Merrillville, IN Part-Time (0-8 hours/week)
About the RoleWe are seeking a Board-Certified Physician to join as a Clinical Research Physician supporting Phase I-IV clinical trials in Merrillville, IN. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies.
Key Responsibilities-
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.
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Conduct medical screenings, physical exams, and assessments of study participants.
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Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
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Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.
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Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
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Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.
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Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
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Contribute to feasibility reviews, study design, and recruitment strategies.
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Stay current with clinical research regulations and therapeutic advances.
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M.D. or D.O. with an active, unrestricted Indiana medical license.
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Board Certification in Endocrinology.
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Valid DEA license and BLS/ACLS certification.
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Clinical research/clinical trials experience preferred (training available for motivated candidates).
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Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
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Excellent communication, collaboration, and interpersonal skills.
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Strong commitment to ethical research and patient-centered care.
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Flexible, part-time schedule (0-8 hours per week).
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Opportunity to expand expertise in multi-therapeutic clinical trials.
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Direct involvement in advancing innovative treatments through research.
About Protouch Staffing
Sourced by ZipRecruiter
Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Frisco, TX, US
Year founded
1989