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Full Time Clinical Research Monitor information

What is a full time clinical research monitor?

Full Time Clinical Research Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they are conducted according to regulatory requirements, ethical standards, and study protocols. They visit research sites to review data, verify patient records, and ensure participant safety. Their work helps confirm the accuracy and integrity of clinical trial results, playing a critical role in the development of new medical treatments and drugs.

What are the key skills and qualifications needed to thrive as a full time clinical research monitor?

To thrive as a Full Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, Good Clinical Practice (GCP) guidelines, and a background in life sciences or nursing, often supported by a bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as ACRP or SOCRA is highly valuable. Outstanding attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring compliance and fostering collaboration among research teams. These competencies are critical for maintaining data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

What are some common challenges full time clinical research monitors face when overseeing multiple clinical trial sites?

Full Time Clinical Research Monitors often encounter challenges such as coordinating communication across multiple sites, managing diverse site staff, and ensuring consistent adherence to protocols and regulatory requirements. Balancing travel, documentation, and follow-up visits can be demanding, especially when sites are geographically dispersed. Strong organizational skills, attention to detail, and effective relationship-building are crucial to ensuring trials progress smoothly and data integrity is maintained.

What cities are hiring for Full Time Clinical Research Monitor jobs?

Cities with the most Full Time Clinical Research Monitor job openings:

What are the most commonly searched types of Clinical Research Monitor jobs?

The most popular types of Clinical Research Monitor jobs are:

What states have the most Full Time Clinical Research Monitor jobs?

States with the most job openings for Full Time Clinical Research Monitor jobs include:

Full Time Clinical Research Monitor jobs near you

Clinical Research Assistant

Headlands Research

Scottsdale, AZ

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago

Job description

 Location: Scottsdale, AZ  | Site Name: Headlands Research Scottsdale  | Full-Time  | Clinical Research

We're seeking a medical assistant for our Research Assistant (RA) position at our clinical research site located in Scottsdale. As an RA, you won't just be supporting research-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, from patient screening to data entry. Your work will directly contribute to the success of new treatments in development.

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Onsite in Scottsdale, AZ (no capabilities for remote or hybrid work)]
Reports to:  Site Director
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.

What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • Opportunities for professional development and career growth
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Responsibilities:

  • Perform intramuscular injections for vaccine studies, when necessary
  • Assist research coordinators in conducting clinical trial visits in compliance with study protocols
  • Collect and record vital signs, make study-related phone calls, and document data in electronic systems
  • Support subject screening, enrollment, and follow-up processes
  • Review and verify study documentation for accuracy and completeness
  • Maintain close communication with coordinators, investigators, and study participants

Requirements:

  • At least one full year of experience providing direct hands-on patient care required
  • Familiarity with medical terminology required
  • Clinical research experience preferred
  • Experience as a phlebotomist, laboratory technician, or medical assistant preferred
  • Comfortable using multiple electronic data entry systems
  • Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment
  • Excellent interpersonal skills-you'll be interacting with participants, providers, and sponsors
  • Passion for improving patient outcomes through research

Apply