Clinical Research Coordinator II

Description

The clinical research company, ObjectiveHealth, is seeking a full-time Clinical Research Coordinator II to relocate to Amarillo, TX. The ideal candidate should have 3+ years of clinical research coordination experience and a strong interest in working directly with patients.

About the role

This role involves taking ownership of assigned studies and patients, communicating promptly and effectively with leadership and coworkers, ensuring compliance with laws, regulations, and requirements, and embodying the company's core values.

Responsibilities

• Taking ownership of assigned studies and patients
• Communicating promptly and effectively with leadership and coworkers
• Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
• Learning and using the technologies provided to increase efficiency in daily activities
• Embodying the company's core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

Requirements

• Legal authorization to work in the US
• 3+ years of clinical research coordination experience
• A strong interest in working directly with patients
• Acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
• Expert communication skills to foster relationships with the research team, PIs, Sponsors, Monitors, and others
• 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

Qualifications

• 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.

Skills

• Effective communication
• Attention to detail
• Compliance with laws, regulations, and requirements
• Use of company-provided technologies to increase efficiency
• Core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

Benefits

• 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 Paid Time Off
• Adoption Assistance
• Paid Holidays
• A wide selection of other voluntary benefits

Pay

Compensation details are competitive and will be discussed during the interview process.

Schedule

The schedule for this role is flexible but will require regular attendance and availability to meet the demands of the position.