Clinical Research Nurse

Flourish Research; Charlotte (NC); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) with match

Tuition reimbursement

Parental leave

Employee referral program

Life insurance

Disability insurance

Generous PTO

Job summary

Flourish Research in Charlotte, NC is seeking a Clinical Research Nurse to support onsite clinical trial activities. The role involves IV infusion, specimen collection, and direct patient care within a compliant, patient-centered research environment.

Qualifications include RN license in NC (ADN/BSN preferred) and 1–2 years of clinical research experience; GCP knowledge is a plus. This is a full-time, on-site position with comprehensive benefits.

Qualifications

• RN license in good standing in NC.
• Graduate of an accredited nursing program (ADN or BSN preferred).
• Proficiency in IV infusion and phlebotomy.
• 1–2 years of clinical research experience preferred.
• Knowledge of FDA regulations and GCP.

Responsibilities

• Perform IV infusion of investigational products and collect blood samples.
• Monitor participants for adverse events during and after infusion.
• Conduct clinical trial visits with participants and support informed consent process.
• Maintain accurate, complete, and protocol-compliant source documentation and records.
• Follow FDA regulations, GCP, and sponsor guidelines; ensure data confidentiality.

Skills

IV infusion

Phlebotomy

Direct patient care

Clinical research

EHR

Education

RN license in NC

ADN/BSN preferred

GCP certification preferred

Tools

Electronic Health Records

eSource

Office365

Job description

About Us:

Flourish Research is where clinical trials thrive.Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WESEEYOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

About the Job:

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.

We are actively hiring a Clinical Research Nurse to supportour Charlotte, NC site.

Shift: Monday-Friday day shift (40 hours per week)

Location: Onsite, Charlotte, NC

FLSA Classification: Non-Exempt

ESSENTIAL JOB FUNCTIONS:

Infusion and specimen collection

• A. Perform IV infusion of blinded and unblinded investigational products according to study protocols.
• B. Obtain blood specimens and other biological samples from study participants following proper clinical procedures.
• C. Monitor participants for adverse events during and after infusion and report findings per protocol and regulatory requirements.
• D. Serve as blinded or unblinded staff as assigned per protocol. When assigned as unblinded staff on a protocol, keep unblinded information separate and do not perform blinded assessments or blinded study tasks on that protocol.

Study conduct

• E. Conduct clinical trial visits by working directly with study participants, ensuring compliance with study protocols, ethical standards and regulatory requirements.
• F. Support participant safety oversight and the informed consent process as delegated by the Principal Investigator.
• G. Collaborate with investigators, study coordinators and other clinical staff to support study start-up, conduct and close-out activities.
• H. Communicate clearly with participants about visit expectations and support a positive participant experience.

Documentation and compliance

• I. Document, manage and maintain research records and source documentation that are accurate, complete, timely and protocol-compliant.
• J. Follow FDA regulations, Good Clinical Practice (GCP) and sponsor guidelines, and support required reporting and documentation activities.
• K. Maintain the confidentiality and integrity of study data and participant information.
• L. Participate in training and maintain current knowledge of clinical trial procedures and safety standards.

General

• M. Represent Flourish Research in a professional and courteous manner (verbal, written and in appearance) when interacting with all staff, clients and vendors.
• N. Additional duties as assigned by management.

PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:

• A. Work is performed on-site in a clinical office setting.
• B. Local travel may be required as needed.
• C. Daily computer use.
• D. Exposure to human bodily fluids.
• E. Participant/patient care.
• F. Occasional evening and weekend work schedules.
• G. Ability to properly lift thirty-five pounds and occasionally more than thirty-five pounds.
• H. Ability to drive and daily availability of an automobile.

MINIMUM REQUIREMENTS:

Education:

• A. Graduate of an accredited nursing program (ADN or BSN preferred).
• B. Current Registered Nurse (RN) license in good standing in the state of the site.
• C. GCP certification preferred.

Experience:

• A. Proficiency in IV infusion and phlebotomy required.
• B. Experience providing direct patient care in a clinical setting required.
• C. 1–2 years of clinical research experience preferred.

Knowledge and Skills:

• A. Knowledge of clinical research methods and the clinical trial process, including informed consent and participant safety oversight.
• B. Knowledge of FDA regulations and GCP, and the ability to apply them in daily study conduct.
• C. Strong attention to detail and documentation accuracy; working knowledge of basic statistical concepts and accurate data collection.
• D. Strong computer skills, including electronic health records, eSource and Office365.
• E. Excellent organizational and time-management skills; able to prioritize competing study tasks and deadlines.
• F. Excellent oral and written communication skills, including clear communication with participants.
• G. Demonstrated ability to collaborate with investigators, coordinators and operations.
• H. Strong problem-solving and risk-assessment abilities; experience reviewing SOPs and improving processes preferred.
• I. Able to think independently and influence when appropriate.

Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.

Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Researchcomplies withthe lawregardingreasonable accommodation for handicapped and disabled employees.