Clinical Research Coordinator at No-Resistance Consulting Group Killeen, TX
No-Resistance Consulting Group
Behavioral Health Market Context
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Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
h the purpose of collecting data to support the device's 510(k) or emergency use approval by the FDA. Notably, the trials we have participated in have directly led to the FDA EUA approval of three separate COVID-19 PCR testing platforms.
No clinical trial experience is required. No Resistance will train the right candidate(s). Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements.
Job Description:
No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.
Job Duties:
• Maintaining regulatory binders, inventory of study-specific and clinical supplies.
• Recruiting, and enrolling study subjects.
• Obtaining informed consent.
• Collecting nasal swab samples.
• Testing samples on investigational laboratory PCR analyzers.
• Data collection and entry.
• Query resolution.
• Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.
Key Success Factors:
• Ability to work independently.
• Desire to work in a clinical environment with direct patient contact.
• Genuine interest in research.
• Timely in all communications.
• Superior attention to detail.
While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply. This position offers an exceptional opportunity to earn a competitive income while gaining invaluable experience highly regarded by medical school admission committees.
Job Type: Full-time
Pay: $22.50 - $25.00 per hour
Expected hours: 40 per week
Benefits:
• 401(k)
• Dental Insurance
• Health Insurance
• Paid time off
• Vision Insurance
Schedule:
• Monday to Friday
Work Location: In person
No clinical trial experience is required. No Resistance will train the right candidate(s). Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements.
Job Description:
No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.
Job Duties:
• Maintaining regulatory binders, inventory of study-specific and clinical supplies.
• Recruiting, and enrolling study subjects.
• Obtaining informed consent.
• Collecting nasal swab samples.
• Testing samples on investigational laboratory PCR analyzers.
• Data collection and entry.
• Query resolution.
• Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.
Key Success Factors:
• Ability to work independently.
• Desire to work in a clinical environment with direct patient contact.
• Genuine interest in research.
• Timely in all communications.
• Superior attention to detail.
While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply. This position offers an exceptional opportunity to earn a competitive income while gaining invaluable experience highly regarded by medical school admission committees.
Job Type: Full-time
Pay: $22.50 - $25.00 per hour
Expected hours: 40 per week
Benefits:
• 401(k)
• Dental Insurance
• Health Insurance
• Paid time off
• Vision Insurance
Schedule:
• Monday to Friday
Work Location: In person
Qualifications
- •No clinical trial experience is required
- •Ability to work independently
- •Desire to work in a clinical environment with direct patient contact
- •Genuine interest in research
- •Timely in all communications
- •While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply
Benefits
- •Pay: $22.50 - $25.00 per hour
- •Expected hours: 40 per week
- •401(k)
- •Dental Insurance
- •Health Insurance
- •Paid time off
- •Vision Insurance
- •Monday to Friday
Responsibilities
- •Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements
- •In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives
- •Maintaining regulatory binders, inventory of study-specific and clinical supplies
- •Recruiting, and enrolling study subjects
- •Obtaining informed consent
- •Collecting nasal swab samples
- •Testing samples on investigational laboratory PCR analyzers
- •Data collection and entry
- •Query resolution
- •Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc
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