Research Nurse (TRI)

Actalent; Orlando (FL); On-site; USD 83,000 - 98,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision Insurance

Life Insurance

Disability Insurance

Paid Time Off from Day One

403-B Retirement Plan

4 Weeks 100% Paid Parental Leave

Career Development

Whole Person Well-being Resources

Mental Health Resources and Support

Pet Benefits

Job summary

Actalent is seeking a Clinical Research Nurse Coordinator in Orlando, FL to support industry-sponsored and investigator-initiated trials. The role involves coordinating trial activities, patient care, data collection, and adherence to FDA regulations and ICH-GCP guidelines.

Responsibilities include managing multiple protocols, coordinating visits, performing nursing procedures (phlebotomy, IVs), and ensuring regulatory compliance.

Qualifications

• ADN required with active Florida RN license.
• BLS certification required.
• Minimum 2 years of clinical research experience.
• Diabetes research or clinical diabetes experience.
• Experience managing clinical trial protocols and documentation.
• Knowledge of FDA regulations, ICH-GCP, HIPAA, and informed consent processes.
• Excellent attention to detail and documentation accuracy.
• Excellent interpersonal and communication skills.
• Ability to work independently while managing competing priorities.
• Ability to adapt to multiple clinical settings based on study requirements.
• Experience administering investigational products.

Responsibilities

• Manage multiple clinical trial protocols from startup through closeout.
• Coordinate participant visits, informed consent, procedures, and follow-ups.
• Perform nursing assessments and clinical procedures, including phlebotomy, IV insertion, and administration of investigational medications.
• Ensure protocol compliance, documentation, and regulatory adherence.
• Maintain study records, investigational products, and materials securely.
• Monitor participant safety and address protocol deviations or safety concerns.
• Collaborate with investigators, sponsors, healthcare providers, and research teams.
• Maintain HIPAA compliance and infection control standards.

Skills

Interpersonal communication

Attention to detail

Independent working

Diabetes research experience

Education

Associate Degree in Nursing (ADN)

Florida RN license

BLS certification

Job description

Monday-Friday 6:45 AM-3:15 PM

The Clinical Research Nurse Coordinator supports clinical research studies by coordinating trial activities, providing patient care, collecting study data, and ensuring compliance with study protocols, FDA regulations, and ICH-GCP guidelines. This role partners with Principal Investigators, research staff, and sponsors to facilitate the successful execution of industry-sponsored and investigator-initiated trials while serving as a strong patient advocate.

Key Responsibilities

Diabetes research experience or knowledge is highly preferred.

• Manage multiple clinical trial protocols from startup through closeout.
• Coordinate participant visits, informed consent, study procedures, and follow up activities.
• Perform nursing assessments and clinical procedures, including phlebotomy, IV insertion, and administration of investigational medications.
• Ensure protocol compliance, accurate documentation, and adherence to regulatory requirements.
• Maintain study records, investigational products, and research materials securely and confidentially.
• Monitor participant safety and elevate protocol deviations or safety concerns as needed.
• Collaborate with investigators, sponsors, healthcare providers, and research teams.
• Maintain clinical readiness, follow HIPAA and infection control standards, and support ongoing regulatory compliance.

Required Qualifications

• Associate Degree in Nursing (ADN)
• Active Florida Registered Nurse license
• Basic Life Support (BLS) certification
• Minimum of 2 years of clinical research experience
• Diabetes research or clinical diabetes experience
• Experience managing clinical trial protocols and research documentation
• Knowledge of FDA regulations, ICH-GCP guidelines, HIPAA requirements, and informed consent processes
• Exceptional attention to detail and documentation accuracy
• Excellent interpersonal and communication skills
• Ability to work independently while managing competing priorities
• Ability to adapt and integrate into multiple clinical settings based on study requirements
• Experience administering investigational products within clinical research environments

Job Type & Location

This is a Permanent position based out of Orlando, FL.

Pay And Benefits

The pay range for this position is $83200.00 - $98000.00/yr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance Paid Time Off from Day One 403-B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits

Workplace Type

This is a fully onsite position in Orlando,FL.

Application Deadline

This position is anticipated to close on Sep 2, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.