You're Viewing 1 Of 95,000+ Jobs On OysterLink

check

New hospitality jobs added daily. Browse by role, pay, or location.

Care Access logo

Travel Clinical Research Coordinator

Job Overview

briefcase

Employment Type

Full-time
moneybag

Compensation

Salary
Range $70,000.00 - $100,000.00
clock

Work Schedule

Standard Hours
diamond

Benefits

Paid Time Off
Company paid holidays
Employer Paid Medical Insurance
employer paid dental insurance
employer paid vision insurance
Health savings account
flexible spending accounts
short-term disability
long-term disability
401(k) retirement plan with company match

Job Description

Care Access is a pioneering healthcare company dedicated to transforming the future of health for communities worldwide. Operating with an extensive network that includes hundreds of research locations, mobile clinics, and a team of skilled clinicians, Care Access brings world-class medical research and health services directly to people who often face barriers to receiving quality care. Focused on accessibility and innovation, Care Access facilitates advanced health screenings and clinical research opportunities through initiatives like the Future of Medicine, which aims to improve health outcomes on a global scale, and Difference Makers, a program designed to empower local leaders to enhance... Show More

Job Requirements

  • Bachelor degree or equivalent education in arts or sciences preferred
  • Fluency in English and Spanish
  • Minimum 3 to 4 years clinical research experience required
  • Minimum 2 years experience as a clinical research coordinator preferred
  • Registered nurse (RN) or licensed practical nurse (LPN) preferred
  • Must be able to travel up to 75 percent nationwide
  • Valid driver’s license and ability to operate rental vehicles
  • Knowledge of ICH/GCP guidelines
  • Strong computer skills including MS Word, Excel, CTMS, and EDC systems
  • Ability to communicate effectively with a diverse team
  • High level of self-motivation and energy
  • Must adhere to FDA regulations and site SOPs
  • Must maintain confidentiality and professional ethics

Job Qualifications

  • Bachelor of science in nursing, pharmacy, or related science preferred
  • Registered nurse (RN) or licensed practical nurse (LPN) preferred
  • Clinical Research Coordinator Certification (CRCC) or exam eligibility preferred
  • Minimum of 3 to 4 years clinical research experience
  • Minimum of 2 years clinical research coordinator experience, management level preferred
  • Proficient in both English and Spanish with excellent written and verbal communication skills
  • Strong knowledge of clinical trials, medicine, and research terminology
  • Familiarity with federal regulations, good clinical practices (GCP), good documentation practices (GDP), and ALCOA-C principles
  • Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) tools
  • Exceptional organizational, prioritization, and leadership skills
  • Critical thinking and problem-solving abilities
  • Ability to work independently in a fast-paced environment
  • Friendly and outgoing personality with a positive attitude under pressure

Job Duties

  • Use Good Clinical Practices (GCP) to screen, enroll, and monitor clinical research study subjects
  • Review and assess study protocols, manuals, and drug brochures for clarity and feasibility
  • Assist Principal Investigators, regulatory teams, and Clinical Trial Managers in training and study setup
  • Coordinate recruitment planning and contact potential study participants
  • Attend investigator meetings, site visits, and monitor visits
  • Maintain organized documentation including source documents, patient charts, and regulatory files
  • Manage investigational product accountability including inventory, dispensing, and patient compliance monitoring
  • Collect, process, and ship biological specimens
  • Communicate sponsor updates, patient progress, and trial management issues
  • Schedule patient visits and ensure proper completion of study procedures
  • Recognize and report adverse and serious adverse events
  • Record data accurately on source documents and electronic case report forms
  • Maintain sponsor correspondence and regulatory documentation
  • Train and supervise assistant staff and ensure adherence to study protocols
  • Travel extensively for study coordination and site management

Job Criteria

Experience

Mid Level (3-7 years)


Job Location

Don't Stop At One Job - There's More

Create a free profile

We'll match you with best jobs

Get job offers faster

Business woman
Business man
Search For More Opportunities:

More Jobs Like This: