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Medical Assistant​/LPN​/Phlebotomist - Clinical Research

Job in Denver, Denver County, Colorado, 80285, USA
Listing for: Medix
Full Time position
Listed on 2026-01-22
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 25 - 27 USD Hourly USD 25.00 27.00 HOUR
Job Description & How to Apply Below
Position: Medical Assistant / LPN / Phlebotomist - Clinical Research
Location: Denver, CO 80238
Pay: $25-27/hr
Duration: ~3 months (seasonal with strong potential to become long-term)
Schedule: Monday-Friday, 8:00 AM - 5:00 PM
Some early mornings and occasional 2-3 hours of overtime (not guaranteed)

Why This Role?

This is a great opportunity to step into the world of clinical research-a fast-growing field where you get to be part of studies that bring new treatments to patients. You'll work on a small, close-knit team, get hands-on experience with research protocols, and learn skills that can open doors to long-term research or clinical careers.

Even if you're new to clinical research, this role is perfect if you have strong clinical skills-especially injections-and want to learn something new.

About the Role

We are hiring for an Unblinded Clinical Research Coordinator I (UCRC I) who will support clinical trials with a focus on managing and administering study medications (Investigational Product or IP). This role blends clinical care, research coordination, and regulatory responsibility.

This position is ideal for a:
  • Medical Assistant
  • LPN
  • Phlebotomist
    with strong injection experience who wants to grow into clinical research.
Key Responsibilities

Clinical & Patient Care
  • Perform injections and administer study medications
  • Interview participants and collect vital signs
  • Perform ECGs and process lab specimens
  • Monitor and document side effects and adverse events
  • Ensure patient safety and protocol compliance
Investigational Product (IP) Management
  • Receive, store, track, dispense, and return study medications
  • Maintain accurate medication accountability logs
  • Monitor storage temperatures daily
  • Maintain strict separation of blinded and unblinded study roles
Documentation & Data
  • Complete source documentation in real time
  • Enter data into Electronic Data Capture (EDC) systems within 48 hours
  • Resolve data queries within 24 hours
  • Track lab and study supplies
Team & Operations
  • Support site readiness and study start-up activities
  • Assist with training backup staff
  • Travel between local sites as needed
Required Qualifications
  • Strong injection experience (required)
  • High School Diploma or GED
  • Ability to work independently in a fast-paced environment
  • Comfortable with computers and documentation
  • Able to lift up to 15 lbs and travel locally
Preferred Qualifications
  • 6 months - 1 year of clinical research experience (but not required)
  • Experience with IP (study drug) handling
  • EDC and/or IRT system experience
  • Medical certification (MA, LPN, Phlebotomist, etc.)
Team & Growth
  • Small, growing team of 2-3 people
  • Opportunity to get in early as the team expands
  • Great exposure to clinical research operations
  • Seasonal role with strong potential to become long-term
Interview Process
  • Virtual interview
  • Quick on-site tour before final decision
Perfect For Someone Who...
  • Loves hands-on clinical work
  • Is confident with injections
  • Wants to break into clinical research
  • Enjoys learning new systems and processes
  • Is excited about being part of something growing
If you're ready to combine clinical skills with research and learn something new, this is the role for you.

Location: Denver, CO 80238
Pay: $25-27/hr
Duration: ~3 months (seasonal with strong potential to become long-term)
Schedule: Monday-Friday, 8:00 AM - 5:00 PM
Some early mornings and occasional 2-3 hours of overtime (not guaranteed)

Why This Role?

This is a great opportunity to step into the world of clinical research-a fast-growing field where you get to be part of studies that bring new treatments to patients. You'll work on a small, close-knit team, get hands-on experience with research protocols, and learn skills that can open doors to long-term research or clinical careers.

Even if you're new to clinical research, this role is perfect if you have strong clinical skills-especially injections-and want to learn something new.

About the Role

We are hiring for an Unblinded Clinical Research Coordinator I (UCRC I) who will support clinical trials with a focus on managing and administering study medications (Investigational Product or IP). This role blends clinical care, research coordination, and regulatory responsibility.

This position is ideal for a:
  • Medical Assistant
  • LPN
  • Phlebotomist
    with strong injection experience who wants to grow into clinical research.
Key Responsibilities

Clinical & Patient Care
  • Perform injections and administer study medications
  • Interview participants and collect vital signs
  • Perform ECGs and process lab specimens
  • Monitor and document side effects and adverse events
  • Ensure patient safety and protocol compliance
Investigational Product (IP) Management
  • Receive, store, track, dispense, and return study medications
  • Maintain accurate medication accountability logs
  • Monitor storage temperatures daily
  • Maintain strict separation of blinded and unblinded study roles
Documentation & Data
  • Complete source documentation in real time
  • Enter data into Electronic Data Capture (EDC) systems within 48 hours
  • Resolve data queries within 24 hours
  • Track lab and study supplies
Team & Operations
  • Support site readiness and study start-up activities
  • Assist…
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