Registered Nurse - Research

Grandview Medical Group

Birmingham (AL)

On-site

USD 70,000 - 100,000

Full time

6 days ago
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Benefits offered by this job

Competitive pay
Medical insurance
Dental insurance
Vision insurance
Life insurance
Generous PTO
Licensure reimbursement
Certification reimbursement
401(k) with company match
Career development
Student loan support
Recognition programs
Collaborative culture
Pet insurance
Identity protection
Legal insurance

Job summary

Grandview Medical Group in Birmingham, AL seeks a Registered Nurse, Clinical Research to coordinate compliant execution of clinical studies, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will collaborate with investigators, study teams, and participants to support study success.

Responsibilities include coordinating study conduct, performing nursing assessments and procedures per protocols, managing recruitment and consent, overseeing regulatory

Qualifications

  • Associate Nursing degree required.
  • 3-5 years of clinical nursing experience.
  • 2-4 years of clinical research experience preferred.
  • Bilingual in Spanish is beneficial.

Responsibilities

  • Coordinate and conduct clinical research protocols per regulatory standards.
  • Perform nursing assessments and procedures per study protocols.
  • Manage subject recruitment, consent, and enrollment.
  • Oversee study documentation and regulatory submissions.
  • Communicate with investigators, sponsors, and regulatory agencies.
  • Ensure data integrity and QA of study documents.
  • Maintain training records, licenses, site certifications, and patient files.
  • Provide education and training to staff and participants.

Skills

Clinical nursing
Regulatory knowledge
Study coordination
Regulatory submissions
GCP compliance
Bilingual Spanish

Education

Associate Degree in Nursing
Bachelor's Degree in Nursing

Tools

EMR systems

Job description

Why Join Us?
  • Be Valued for What You Bring to the Team - Competitive pay that rewards your hard work
  • Benefits You Can Count On - Medical, dental, vision, and life insurance coverage
  • Work Hard. Recharge Often. - Generous PTO and extended illness benefits
  • Invest in Your Future - 401(k) with company match
  • Grow With Us - Career development, learning opportunities, and advancement pathways
  • We Invest in Your Success - Licensure and certification reimbursement
  • Student Loan Support - Assistance available for eligible roles
  • Your Wins Deserve Recognition - Employee rewards and recognition programs
  • A Team You'll Love Working With - A collaborative, purpose-driven culture making a difference every day
  • Additional Voluntary Benefits - Choose from options such as pet insurance, identity protection, and legal insurance. Great people. Great benefits. Meaningful work. Join us and make an impact
Job Summary

The Registered Nurse, Clinical Research coordinates and manages the compliant execution of clinical research studies, ensuring adherence to protocols, regulatory requirements, and ethical standards. This role involves collaborating with investigators, research teams, and participants to ensure the successful implementation of studies.

Essential Functions
  • Coordinates the implementation and conduct of clinical research protocols, ensuring compliance with protocol requirements, regulatory standards, and timelines.
  • Performs clinical assessments, treatments, and procedures within the Registered Nurse scope of practice as required by research protocols, including administration of medications, patient monitoring, and follow-up care.
  • Manages subject recruitment, screening, informed consent, and enrollment, ensuring eligibility criteria are met and participants are informed of study details.
  • Oversees study documentation, including regulatory submissions, case report forms, and data collection, ensuring accuracy and adherence to Good Clinical Practice (GCP) and FDA guidelines.
  • Acts as a liaison between investigators, research staff, sponsors, and regulatory agencies, addressing protocol-related questions and ensuring effective communication.
  • Conducts quality assurance reviews of study documents and regulatory submissions, identifying areas for improvement and ensuring data integrity.
  • Maintains essential regulatory and study documentation, including training records, licenses, site certifications, and patient files, to support audits and inspections.
  • Provides education and training to research staff and participants regarding protocol requirements, study expectations, and safety monitoring.
  • Performs other duties as assigned.
  • Maintains regular and reliable attendance.
  • Complies with all policies and standards.
Qualifications
  • Associate Degree in Nursing required
  • Bachelor's Degree in Nursing preferred
  • 3-5 years of clinical nursing experience required
  • 2-4 years of clinical research experience preferred
Knowledge, Skills and Abilities
  • Strong understanding of clinical research protocols, regulations, and ethical guidelines, including FDA and NIH requirements.
  • Proficiency in managing study documentation, regulatory submissions, and data collection.
  • Clinical expertise in assessments, treatments, and nursing care within research settings.
  • Effective communication and interpersonal skills for collaboration with multidisciplinary teams, sponsors, and participants.
  • Attention to detail and organizational skills to manage multiple studies and regulatory requirements.
  • Ability to analyze and solve complex problems in a dynamic research environment.
  • Knowledge of electronic data management systems and medical record systems preferred.
  • Bilingual (Spanish) is beneficial.
Licenses and Certifications
  • RN - Registered Nurse - State Licensure and/or Compact State Licensure required
  • BCLS - Basic Life Support obtained within the first 12 months of employment required

This position is not eligible for immigration sponsorship now or in the future. Applicants must be authorized to work in the U.S. for an employer.

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