Part-Time Clinical Research Nurse

Job Description

Job Description

Job Title: Clinical Research Nurse – Oncology Trial (Mobile, AL)

Job Description

This role is an on-site Clinical Research Nurse position supporting an oncology clinical trial at a dedicated research site in Mobile, AL. The nurse will contribute to all aspects of trial execution, including patient pre-screening, data entry and verification, electronic diary compliance, lab kit support, participant follow-up, and study visit preparation. This is a full-time, 40-hour-per-week contract role lasting approximately seven months, ideal for a clinical research professional who is detail-oriented, organized, and experienced in oncology research and electronic medical records.

Responsibilities

• Support all clinical and operational tasks associated with an oncology research trial at the site.
• Pre-screen patients for eligibility and review charts to confirm inclusion and exclusion criteria.
• Perform accurate and timely data entry into clinical trial databases and electronic systems.
• Verify data for completeness, accuracy, and consistency, and resolve data queries as needed.
• Monitor and support participant compliance with electronic diaries (e-diaries).
• Prepare lab kits and support specimen collection, processing, and documentation in accordance with protocol.
• Coordinate and conduct participant follow-up activities, including scheduling and tracking study visits.
• Prepare for study visits by organizing required documents, supplies, and equipment.
• Collaborate with clinical research coordinators and other site staff to ensure smooth trial operations.
• Utilize electronic medical records (EMR) systems to review and document participant information.
• Assist with recruitment activities to identify and enroll eligible participants.
• Adhere to Good Clinical Practice (GCP) guidelines, HIPAA regulations, and site-specific standard operating procedures.
• Maintain meticulous attention to detail in all aspects of documentation and trial conduct.
• Contribute to a fast-paced research environment by prioritizing tasks and meeting protocol timelines.

Essential Skills

• Minimum of 2 years of experience working as a Clinical Research Nurse.
• Demonstrated experience in clinical research, preferably in oncology trials.
• Proficiency with electronic medical records (EMR) systems.
• Strong data entry skills with a focus on accuracy and completeness.
• Experience in patient pre-screening and chart review for clinical trials.
• Knowledge and application of Good Clinical Practice (GCP) guidelines.
• Training in HIPAA regulations and patient privacy requirements.
• Ability to manage e-diary compliance and support participants in using electronic tools.
• Competence in verifying clinical trial data and resolving queries.
• Strong organizational skills and attention to detail in a fast-paced environment.
• Ability to work full-time (40 hours per week) for the duration of a 7-month contract.

Additional Skills & Qualifications

• Experience in oncology or experience supporting oncology clinical trials.
• Experience working as or closely with a Clinical Research Coordinator.
• Familiarity with recruitment strategies for clinical trial participants.
• Ability to collaborate effectively with multidisciplinary clinical and research teams.
• Comfort with handling lab kits and supporting specimen-related procedures under protocol guidance.
• Strong communication skills for interacting with participants and documenting clinical information.
• Ability to prioritize multiple tasks while maintaining high-quality documentation.

Work Environment

The role is based on-site at a clinical research facility in Mobile, AL, operating during normal business hours with a 40-hour workweek. The environment is fast-paced and detail-oriented, requiring consistent focus on accuracy, regulatory compliance, and protocol timelines. The Clinical Research Nurse will work closely with coordinators and other research staff, using electronic medical records and trial-specific systems to manage participant data and study documentation. Professional clinical attire appropriate for a research and healthcare setting is expected.

This is a Contract position based out of Mobile, AL.

The pay range for this position is $25.00 - $35.00/hr.

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)

This is a fully onsite position in Mobile,AL.

This position is anticipated to close on Jul 27, 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 View email address on ziprecruiter.com 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.