Registered Nurse

Actalent is Hiring a Team of Registered Nurses for Clinical Research Facility!

Job Description The RN coordinates, supervises, and monitors clinical research study activities to ensure high-quality data collection and consistent adherence to Good Clinical Practice (GCP) standards. This role focuses on safeguarding participant safety, overseeing clinical operations and screening processes, and supporting the successful execution of clinical trials within a clinical setting. It offers an exciting opportunity to gain or expand experience in clinical research with a global organization. Responsibilities

- Coordinate and supervise day-to-day study activities to ensure all procedures follow the study protocol and Good Clinical Practice (GCP) standards.
- Monitor and maintain a high standard of data collection and documentation to support accurate and reliable study outcomes.
- Ensure participant safety at all times by closely monitoring clinical results, compliance, and safety issues that may require exclusion or discontinuation from the study.
- Supervise staff and study events on the unit in accordance with protocol requirements, providing direction and oversight during all study phases.
- Make staffing adjustments during absences or unanticipated work circumstances to maintain appropriate coverage and continuity of care.
- Monitor study schedules and review study activities as they progress to ensure timelines and protocol requirements are met.
- Review, record, and follow up on adverse events, ensuring timely documentation and appropriate communication with the study team.
- Confirm that a complete screening chart, including informed consent forms, laboratory results, and Investigator approval, is available on the day of admission for every subject.
- Monitor clinical results and participant compliance to identify any safety issues or protocol deviations that may affect continued participation.
- Effectively interact with pharmaceutical company representatives and clinical research organizations in response to queries during the course of the research study.
- Participate in protocol meetings with pharmaceutical company representatives to review study requirements, procedures, and expectations.
- Ensure all necessary source documents are available on the unit in a timely manner to support ongoing study activities.
- Review study source documents for completeness and accuracy, addressing any missing or inconsistent information.
- Assist with training and orienting new employees, including regular and per diem staff, by providing guidance on general study procedures and clinical trial processes.

Essential Skills

- Registered Nurse (RN) with at least 1 year of experience, preferably in a clinical research environment or patient care setting.
- Experience in clinical research, patient care, or case management that supports coordination and oversight of clinical activities.
- Strong computer skills, including the ability to accurately document study findings and adverse events in electronic or paper-based systems.
- Ability to monitor and interpret clinical results and safety data to support participant safety and protocol compliance.
- Strong organizational skills to manage study schedules, documentation, and multiple concurrent tasks.
- Effective communication skills to interact professionally with staff, study participants, pharmaceutical representatives, and clinical research organizations.
- Ability to supervise and support clinical staff in a study environment, including making staffing adjustments when needed.

Additional Skills & Qualifications

- Experience in clinical research, case management, or medical-surgical nursing is highly relevant.
- Fluency in both English and Spanish is preferred but not required.
- Familiarity with Good Clinical Practice (GCP) standards and clinical trial operations.
- Ability to participate in and contribute to protocol meetings with external stakeholders.
- Comfort working in a bilingual environment and engaging with diverse participant populations.

Work Environment This role is based in a clinical setting focused on the conduct of clinical research studies. The Study Nurse Coordinator works closely with clinical staff, investigators, and external partners such as pharmaceutical company representatives and clinical research organizations. The environment involves direct interaction with study participants, use of clinical equipment, and regular use of computer systems for documentation and data entry. The position provides exposure to global clinical research operations and offers a structured, professional atmosphere where adherence to protocols, safety standards, and regulatory requirements is essential.
Job Type & Location
This is a Contract to Hire position based out of Miami, FL.
Pay and Benefits
The pay range for this position is $30.00 - $36.00/hr. 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. Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Job Type & Location
This is a Contract to Hire position based out of Miami, FL.
Application Deadline
This position is anticipated to close on Nov 3, 2026.
Workplace Type
This is a fully onsite position in Miami,FL. 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 [email protected] 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.