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:
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
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:
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
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.
*We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).
*As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
