Clinical Research Nurse III

Clinical Research Nurse III

Duration: 12-Month Contract-to-Hire

Schedule: Primarily Onsite | Standard business hours beginning between 7:00 AM and 9:00 AM Required Qualifications

- Active Registered Nurse (RN) license in the State of Georgia
- One of the following: Four (4) years of research nursing experience;

OR

- Four (4) years of clinical nursing experience PLUS two (2) years of clinical research experience
- Must have Oncology nursing experience
- Clinical research and clinical trial experience
- Experience working within Good Clinical Practice (GCP) guidelines
- Strong knowledge of adverse event (AE) and serious adverse event (SAE) reporting
- Strong communication, organizational, and patient education skills
- Experience leading complex oncology clinical trial protocols
- Knowledge of FDA regulations and clinical research compliance requirements
- Experience supporting sponsor monitoring visits, audits, and regulatory inspections
- Experience contributing to publications, grants, presentations, or research initiatives

Key Responsibilities Clinical Research Leadership

- Lead clinical coordination activities for complex oncology research protocols.
- Independently manage study participants and protocol-related clinical activities.
- Ensure compliance with protocol requirements, FDA regulations, GCP standards, and organizational policies.
- Serve as a subject matter expert on clinical research procedures and participant safety.

Patient Care & Study Management

- Conduct protocol-required patient visits, assessments, and clinical evaluations.
- Educate patients and families regarding study participation, treatment plans, and research requirements.
- Monitor, document, and report adverse events (AEs) and serious adverse events (SAEs).
- Ensure participant safety and protocol adherence throughout all phases of study participation.

Regulatory & Sponsor Support

- Collaborate with investigators, physicians, research coordinators, sponsors, and multidisciplinary clinical teams.
- Support sponsor monitoring visits, audits, inspections, and regulatory reviews.
- Maintain accurate source documentation and study records.
- Assist with the development and implementation of study materials and operational processes.

Mentorship & Process Improvement

- Train and support research staff and study personnel.
- Mentor junior research nurses and coordinators.
- Participate in process improvement initiatives that enhance research operations and patient experience.
- Serve as a resource for research compliance, policies, procedures, and best practices.

Research Contributions

- Support publications, presentations, grant activities, and other research initiatives.
- Contribute to the advancement of innovative oncology therapies and clinical research programs.
Job Type & Location
This is a Contract to Hire position based out of Atlanta, GA.
Pay and Benefits
The pay range for this position is $43.00 - $45.00/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 Atlanta, GA.
Application Deadline
This position is anticipated to close on Nov 5, 2026.
Workplace Type
This is a fully onsite position in Atlanta,GA. 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.