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Freelance Clinical Study Startup Jobs in Colorado

Syneos Health

Medical Science Liaison

Denver, CO · On-site

$190 - $210/hr

Partner with Clinical Development, Clinical Operations, CRO partners, and investigative sites to support effective study startup, protocol understanding, and trial execution. * Execute nonpromotional ...

Syneos Health, Inc.

Medical Science Liaison

Denver, CO · On-site

$190 - $210/hr

Partner with Clinical Development, Clinical Operations, CRO partners, and investigative sites to support effective study startup, protocol understanding, and trial execution. * Execute nonpromotional ...

The US Oncology Network

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

Planning and tracking of all assigned clinical activity in the lifecycle phases of the startup ... Creates study specific tools for source documentation as well as checklists and clinic information ...

The US Oncology Network

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

Planning and tracking of all assigned clinical activity in the lifecycle phases of the startup ... Creates study specific tools for source documentation as well as checklists and clinic information ...

Flourish Research

Oncology Training Manager

Denver, CO · On-site

$88K - $100K/yr

Provide structured, hands-on training to oncology clinical research staff on study workflows ... Embed with site teams during study startup to deliver early-phase protocol walkthroughs, support ...

Flourish Research

Oncology Training Manager

Denver, CO · On-site

$88K - $100K/yr

Provide structured, hands-on training to oncology clinical research staff on study workflows ... Embed with site teams during study startup to deliver early-phase protocol walkthroughs, support ...

Flourish Research

Oncology Training Manager

Denver, CO · On-site

$88K - $100K/yr

Provide structured, hands-on training to oncology clinical research staff on study workflows ... Embed with site teams during study startup to deliver early-phase protocol walkthroughs, support ...

Flourishresearch

Clinical Team Lead (Oncology)

Denver, CO · On-site

$90 - $109.99/hr

Lead study conduct, including accurate and timely data entry into EMR, EDC, CTMS, and other ... Ability to work independently and as part of a team in a startup and/or high‑growth environment.

Amgen

Imaging Specialist Manager

Denver, CO · On-site +1

... clinical trials across all phases from study start-up to close-out. Responsabilities: * Provide oversight and expertise for imaging setup and startup activities * Maintain the quality and scientific ...

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Freelance Clinical Study Startup information

What is the difference between Freelance Clinical Study Startup vs Clinical Research Associate?

AspectFreelance Clinical Study StartupClinical Research Associate
CredentialsTypically requires knowledge of clinical trial processes, basic certifications, or relevant experienceRequires a degree in life sciences or healthcare, and often certifications like CCRP or RAC
Work EnvironmentIndependent, project-based, often remote or on-site at trial locationsUsually employed by sponsors or CROs, working on-site or remotely within a structured team
Employer & Industry UsageFreelance roles in biotech, pharma, or CROs managing startup phases of trialsFull-time or contract roles within pharmaceutical companies or CROs overseeing trial conduct

In summary, a Freelance Clinical Study Startup focuses on initiating and managing early trial phases independently, while a Clinical Research Associate typically works within a team to monitor ongoing trials, requiring more formal certifications and a structured work environment.

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Freelance Clinical Study Startup jobs near you

Senior Clinical Research Coordinator

Crox Consulting Inc

Denver, CO • On-site

$70K - $85K/yr

Full-time

Re-posted 10 days ago

Job description

OVERVIEW

This role will coordinate research in an exciting new environment, with the full backing of a new type of research architecture and a top-tier technology team, challenging the paper-heavy, old-school way that studies are run. This role will require the desire to learn and grow rapidly, and include the opportunity to help spearhead on-site efforts for companies partner healthcare groups. This role will be evaluated on provider success, patient experience, protocol management and adherence, and data quality. This role will require a track record of excellence as a Research Assistant or CRC or other similar role, including developing successful relationships with providers. You will need to be able to thrive with multiple balls in the air, and where independent problem solving is a daily need. You will need to lead with empathy for patients, and care deeply about creating new access to clinical research in communities across the country. 

KEY RESPONSIBILITIES 

  • Act as senior study coordinator to execute trials conducted within physician practices, including but not limited to: 
a. Visit preparation activities 
b. Visit follow-up activities 
c. Supply and inventory management 
d. Third party vendor management 
  • Conduct patient recruitment and enrollment of eligible patients. 
  • Lead patient study visits, which may also include clinical and lab procedures such as ECG, phlebotomy, vitals signs and body measurements, laboratory processing, etc. 4. Independently administer the informed consent process with care and quality 5. Ensure protocol adherence and high data integrity 
  • Provide high quality source data capture and documentation 
  • Support study start-up and planning, including PSVs and SIVs 
  • Support IRB submission and correspondence 
  • Facilitate monitoring visits (IMVs) and sponsor correspondence including managing the follow-up process 
  • IP management, dispensation and accountability 
  • Adverse Event management, tracking, and follow-up 
  • Data entry to CRF/EDC and query resolution in a timely manner 
  • Support study close-out, including COVs 
  • Protocol deviation tracking, reporting, and reconciliation 
  • Train and mentor junior research staff
  • Using and helping improve companies proprietary tool set 
  • Data Quality-understand and comply with all regulations, policies, and guidelines applicable to clinical research, including our SOPs 
  • Ensure adherence to study protocols while ensuring trial staff maintain meticulous accuracy in completing all documentation 
  • Conduct Quality Control activities including routine QC checks during and following study visits 
  • Any other duties assigned by manager 

MINIMUM QUALIFICATIONS 

  • Bachelor's degree or equivalent combination of training and experience
  • 5+ years of experience as a Clinical Research Coordinator, Research Assistant, or other similar role 
  • 5+ years of experience independently coordinating studies, from study startup to close out
  • 5+ years demonstrated track record of delivering clean data and a high-quality patient experience
  • Expert knowledge of FDA regulations and ICH/GCP guidelines 
  • Strong communication skills, teamwork, cooperation, self-awareness, and flexibility
Job Roles and Responsibilities
  • CRIO CTMS
  • Patient Follow-up
  • Patient Visits
  • Phlebotomy
  • Phlebotomy/ECT
  • Physician Relationships
  • Chart Review