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Clinical Research Assistant
Presbyterian Healthcare Services. Assist the research nurse/coordinator in conducting clinical trials .
Posted 10/5/2026full-timeAlbuquerque • New Mexico • United StatesJuniorMid-Level💰 $23 - $39 per hourWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting clinical trials, including specimen collection, data entry, and maintaining organized records for audits. Proficient in phlebotomy and managing clinical data collection, ensuring compliance with study protocols.
Highest-signal resume keywords
Clinical Trials AssistancePhlebotomy SkillsData Entry in Sponsor PortalsClinical Data CollectionCertified Phlebotomist
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Data CollectionPhlebotomyData EntrySpecimen HandlingVital Signs MeasurementEKG RecordingMedical Record RetrievalCase Report Form DocumentationOrganized Record MaintenanceStudy Patient Scheduling
Soft Skills
CommunicationOrganizational SkillsAttention to DetailTriage Management
Tools & Technologies
Sponsor PortalsLaboratory Equipment
Certifications & Qualifications
Certified PhlebotomistMedical Assistant Certification
Industry Keywords
Clinical TrialsResearch ExperienceSpecimen ProcessingClinical SpecimensStudy Protocols
About the role
Key responsibilities & impact- Assist the research nurse/coordinator in conducting clinical trials
- Collect, process, store, and handle clinical specimens
- Schedule study patients for follow-up and study appointments
- Collect, record, and file clinical data
- Document information on case report forms
- Retrieve medical records
- Collect clinical data such as vital signs, EKG recordings, and weights
- Perform phlebotomy and transport specimens to the laboratory
- Enter data in sponsor portals
- Maintain accurate files and organized records for sponsor audits
- Collect source documents
- File and pull study records for physicians, research nurses, and study monitors
- Triage research-related phone calls
- Manage long-term follow-up
- Perform other functions as required
Requirements
What you’ll need- HS/GED
- 2 yrs of research experience; or Medical Assistant (prefer certified)/Laboratory Technician with at least 6 months of clinical experience
- Preferred Qualification: Certified Phlebotomist
- Ability to perform phlebotomy as directed by the study plan
- Ability to accurately enter data in sponsor portals
- Ability to collect, process, store, and ship blood/tissue specimens
- Ability to retrieve electronic and/or paper medical records
- Ability to collect clinical data such as vital signs, EKG recordings, and weights
Benefits
Comp & perks- Medical insurance
- Dental insurance
- Vision insurance
- Short-term disability insurance
- Long-term disability insurance
- Group term life insurance
- Optional voluntary benefits
- Employee Wellness rewards program
- Gift cards and other rewards for participating in wellness activities