Must Haves:
- 1+ years of Experience with clinical trials
- Industry Sponsored Clinical trial experience
- Family and drug/device studies experience
- Patient Contact Experience
- Have a car to get them to other locations
Plusses:
- Psych and mental health
- Neurology
- Phlebotomy Experience
- CCRP Certified / Socra Certified
- CRO experience
- Epic Experience
- CITI trained
- EKG Experience
- Experience with phase 1- phase 4
Day to Day:
Communication and Coordination:
- Check Emails and Voicemails: Start the day by reviewing emails and voicemails. Look for responses from potential funders, trial candidates, or medical professionals.
- Coordinate with Key Personnel: Collaborate with the Principal Investigator (PI), department, and central administration to ensure that clinical research activities comply with federal regulations and university policies.
Study Preparation and Administration:
- Feasibility Assessments: Assist the PI in assessing the feasibility of conducting the study at specific sites.
- Standard Operating Procedures (SOPs): Develop SOPs for study-related activities.
- Database Programs and Forms: Create necessary study forms and database programs for data collection and entry.
- Training: Train medical assistants and nurses on study protocols.
- IRB Correspondence: Review and prepare correspondence with the Institutional Review Board (IRB) for submissions, amendments, adverse events, and progress reports.
- Regulatory Compliance: Maintain regulatory documents as per sponsor and IRB protocols.
Participant Interaction and Study Activities:
- Eligibility Screening: Screen potential subjects for study eligibility.
- Recruitment and Retention: Coordinate recruitment efforts and ensure retention of research subjects.
- Informed Consent: Participate in the informed consent process with study participants.
- Study Activities: Perform face-to-face and telephone assessments, medical records abstraction, and other study-related tasks.
- Specimen Handling: Collect, process, and ship specimens as needed.
- Appointment Scheduling: Coordinate diagnostic tests and procedures associated with study protocols.
Document Management and Accountability:
- Document Control: Ensure study documents are complete, current, and filed correctly.
- Time and Effort Recording: Accurately record time and effort spent on study-related tasks.
- Medication Management: Be responsible for study medication accountability and maintenance. This may involve dispensing study meds to patients, coordinating storage, and ensuring compliance with the study protocol.
Job Type: Full-time
Pay: $62,000.00 - $65,000.00 per year
Benefits:
- Dental insurance
- Health insurance
- Vision insurance
Experience level:
Schedule:
- 8 hour shift
- Monday to Friday
Experience:
- Clinical research: 1 year (Required)
- Patient facing: 1 year (Required)
- Psych/ mental health: 1 year (Preferred)
- Neuro: 1 year (Preferred)
License/Certification:
Ability to Commute:
- Evanston, IL 60201 (Required)
Ability to Relocate:
- Evanston, IL 60201: Relocate before starting work (Required)
Work Location: In person