You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients. 

This is a full time, in-person role in Atlanta GA

Job Summary

Our client is seeking a dedicated Clinical Research Nurse to independently manage significant aspects of clinical trials, oversee data, and ensure compliance with applicable regulations. This role involves direct interaction with research participants and sponsors, resolving study issues, providing leadership, and offering guidance to less experienced staff.

Key Responsibilities

• Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects.
• Trains and provides guidance to less experienced staff.
• Oversees data management for research projects.
• Interfaces with research participants and resolves issues related to study protocols.
• Authorizes purchases for supplies and equipment maintenance.
• Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.
• Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes.
• Monitors IRB submissions and responds to requests and questions.
• Interfaces with study sponsors, monitors and reports SAEs; resolves study queries.
• Provides leadership in determining, recommending, and implementing improvements to policies/processes.
• Assists in developing grant proposals and protocols.
• With appropriate credentialing and training, may perform phlebotomy, specimens collection or diagnostics.
• May perform some supervisory duties.
• Performs related approved responsibilities as required.

Qualifications

• CRN Experience.
• Approximately 2–3 years of solid interventional drug trial experience.
• Must have experience managing multiple trials and patients.
• Ability to manage complex Phase I inpatient trials.
• Therapeutic drug experience is highly valued.
• Ability to perform effectively without extensive foundational training.

Experience

• 2–3 years of solid interventional drug trial experience required.
• Experience managing multiple trials and patients.

Skills

• Data management.
• Compliance auditing.
• IRB submission monitoring.
• SAE reporting.
• Study query resolution.
• Leadership and guidance.
• Grant proposal development support.
• Phlebotomy skills (preferred).
• Specimen collection (if credentialed and trained).
• Diagnostics (if credentialed and trained).

Education

• BSN, RN Certification
• CRC Experience.

Additional Requirements

• Work schedule: Monday-Friday, 8 AM - 5 PM.
• Full time, in person role in Atlanta GA

Benefits

• Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances).
• Health Benefits / Dental / Vision (Medix offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan. Eligibility for health benefits is based on verifying that an average of 30 hours per week during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s)).
• 401k (Eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1).
• Short Term Disability Insurance.
• Term Life Insurance Plan.

Required Employment / Compliance Language

Medix is an equal opportunity employer and does not discriminate on the basis of race, color, religion, age, sex, national origin, disability, veteran status, sexual orientation, or any other status protected by law. All employment decisions are made based on qualifications, merit, and business needs. As part of our commitment to diversity and inclusion, we encourage all qualified candidates to apply.

^*We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).

Medix Overview:

With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we’re dedicated to creating opportunities for job seekers at some of the nation's top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.

^*As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.