Qureos Mentor

Headlands Research

<div><div>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</div><h1 class="jobSectionHeader">
Clinical Research Assistant</h1>

 Location: Escondido, CA | Site Name: AMCR Institute | Per Diem/PRN | Clinical Research

We're seeking a Clinical Research Assistant (RA) for our clinical research site AMCR Institute located in Escondido, CA. As an RA, you won't just be supporting research&mdash;you'll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field. 


 The Role:

As a Clinical Research Assistant, you'll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution&mdash;from subject screening to data entry. Your work will directly contribute to the success of new treatments in development. 


Type: Per Diem/PRN 
Location: Onsite in Escondido, CA (no capabilities for remote or hybrid work) 


Responsibilities:
<ul>
<li>Assist research coordinators in conducting clinical trial visits in compliance with study protocols</li>
<li>Collect and record vital signs, make study-related phone calls, and document data in electronic systems</li>
<li>Support subject screening, enrollment, and follow-up processes</li>
<li>Review and verify study documentation for accuracy and completeness</li>
<li>Maintain close communication with coordinators, investigators, and study participants</li></ul> 


Requirements:
<ul>
<li>Familiarity with medical terminology and basic laboratory procedures required</li>
<li>Prior experience providing direct hands-on patient care required</li>
<li>Clinical research experience preferred</li>
<li>Comfortable using multiple electronic data entry systems</li>
<li>Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment</li>
<li>Excellent interpersonal skills&mdash;you'll be interacting with participants, providers, and sponsors</li>
<li>Passion for improving patient outcomes through research</li></ul></div>

Per Diem/PRN Clinical Research Assistant

<div><div>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</div>
Why is it that as medicine advances, people aren't feeling better?

More importantly, why aren't doctors feeling better?

The system is overworked.

You are overworked.

But you don't have to let your medical career get eaten up by the beast. 


Clinvest/Headlands Research is inviting you back to the way things ought to be:
<ul>
<li>Where patients get the time, they need</li>
<li>Where the status quo of treatment is always challenged</li>
<li>Where physicians have the time and space to be excellent on the job, and at home</li></ul> 


Specifically, we are searching for a M.D./D.O. to lead our Southwest Missouri research clinic, and work hand in hand with those suffering from migraine, diabetes, arthritis, metabolic, and cardiovascular diseases.

As the leader of our clinical trials, you will work with a dedicated team of nurses and coordinators to research the impact of phase 2-4 pharmaceuticals.

For many patients, you will be the miracle doctor who finally helped them find the missing piece of the puzzle.

For the world of medicine, you will be honored as a partner in a better tomorrow.

And for your family, you will have more time to be present, because this company values your life outside of work. 


If you are:
<ul>
<li>Missouri License Eligible</li>
<li>Someone who pays attention to the details</li>
<li>Tired of the status quo in the medical industry</li>
<li>Someone who thrives on unique challenges</li>
<li>Someone who loves leading a team</li>
<li>Looking to make a bigger impact on your patients</li>
<li>Wanting an opportunity to collaborate with other key opinion leaders and experts in the network and the medical field</li>
</ul>
We want to talk to you!</div>

Investigator, MD/DO

<div><div>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</div> 

<h1 class="jobSectionHeader">
Clinical Research Coordinator (CRC)</h1>

 Location: Escondido, CA | Site Name: Headlands Research - AMCR | Full-Time 


Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Escondido, CA. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.

Type: Regular Full-time Employee 
Schedule: Mondays through Fridays, 8:00am - 5:00pm 
Location: Onsite in Escondido, CA (no capabilities for remote or hybrid work) 
Reports to: Clinical Trial Manager 
Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.
<h2 class="jobSectionHeader">
 What We Offer</h2>
<ul><li>Competitive pay + annual performance incentives</li>
<li>Medical, dental, and vision insurance</li>
<li>401(k) plan with company match</li>
<li>Paid time off (PTO) and company holidays</li>
<li>A mission-driven culture focused on advancing medicine and improving patient outcomes</li></ul> 


<h2 class="jobSectionHeader"> Why Join Us?</h2>

You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster&mdash;while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you. 


Responsibilities: 

<ul>
<li>Coordinate all aspects of assigned clinical trials from site initiation to study close-out</li>
<li>Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards</li>
<li>Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs</li>
<li>Manage subject recruitment, informed consent, and retention strategies</li>
<li>Ensure timely data entry and resolution of EDC queries</li>
<li>Report and follow up on all adverse events, serious adverse events, and deviations</li>
<li>Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders</li>
<li>Prepare for and participate in monitoring visits, audits, and inspections</li>
<li>Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems</li>
<li>Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)</li>
<li>Attend investigator meetings and provide cross-functional support as needed</li>
<li>Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control</li></ul> 


Requirements: 

<h2 class="jobSectionHeader">
 Education &amp; Experience Requirements</h2>
<ul><li>Required: High school diploma or GED</li>
<li>Experience:
<ul><li>Minimum of 1 year of experience as a Clinical Research Coordinator OR</li>
<li>Minimum of 2 years of college within a health-related program OR</li>
<li>Licensed as a Licensed Practical Nurse (LPN) or higher OR</li>
<li>Bachelor's degree in a health or scientific-related program</li>
</ul> </li></ul><h2 class="jobSectionHeader">Skills &amp; Qualifications</h2>
<ul><li>Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures</li>
<li>Proficiency in medical terminology and clinical documentation practices</li>
<li>Strong interpersonal, verbal, and written communication skills</li>
<li>Organized, detail-oriented, and capable of managing multiple priorities</li>
<li>Proficient in Microsoft Office and other clinical research systems</li></ul> 


 Apply now to become a part of a team that's changing the future of healthcare&mdash;one trial at a time.</div>

Clinical Research Coordinator

Join Headlands Research and explore 3   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Headlands Research

ABOUT_COMPANY

Per Diem/PRN Clinical Research Assistant

Investigator, MD/DO

Clinical Research Coordinator