Top 8 Clinical research associate Jobs in Amarillo, Tx

Clinical Research Coordinator II
ObjectiveHealth —Amarillo, TX
- Full-time
- Blood sampling
- Mid-level
- 3 years
- Paid holidays
- Disability insurance
Quick Apply
Cinical Research Coordinator I
ObjectiveHealth —Amarillo, TX
- Full-time
- Mid-level
- Clinic
- US work authorization
- Paid holidays
- Disability insurance
Quick Apply
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Amarillo, TX
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification

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Clinical Research Coordinator II

ObjectiveHealth -
Amarillo, TX

Quick Apply

Job Details

Full-time

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Adoption assistance
Vision insurance
401(k) matching

Qualifications

Direct patient care
Blood sampling
Adverse event reporting
Regulatory compliance
Medication pass administration
Mid-level
ECG equipment
3 years
Research project coordination
Clinical data entry
Research compliance clinical trial records management
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
Patient interaction
Medical assisting
IRB compliance
Patient treatment
Ethical review application preparation
Legal compliance
Communication skills
Project stakeholder communication
Physical assessments
Cross-functional communication
Quality data entry

Full Job Description

Description:

Clinical Research Coordinator II

Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ years of clinical research coordination experience, and have a strong desire to work directly with patients.

Who We Are

ObjectiveHealth is a clinical research company that uses proprietary technology to:

Increase patient access to research trials within our communities,
Provide physicians with enhanced care options for current patients, and
Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Who You Are

A lover of patient interaction and skilled at providing patient care
A team player with a bias for action and an attitude that takes personal responsibility
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
A strong advocate for Company values, mission, and initiatives
Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology

What Success Looks Like for This Role

Taking ownership of assigned studies and patients
Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
Showing up on time, every time
Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
Learning and using the technologies we provide to increase efficiency in your day-to-day activities
Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

What We Offer

Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.

Requirements:

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.

Quick Apply

Refine Your Search

clinical research associate jobs in amarillo, tx

Clinical Research Coordinator II

Cinical Research Coordinator I

Per Diem Clinical Research Nurse - Home Visits

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