Clinical Research Coordinator

Job Title: Part-Time Clinical Research Coordinator

Hours: 20 per week (flexible Monday-Friday)

Duration: Contract until November 2026

Job Description

This position offers an opportunity for an experienced Clinical Research Coordinator to support an RSV vaccine clinical trial at a dedicated research site. The role focuses primarily on patient recruitment activities for an RSV vaccine study, ensuring that participants are identified, pre-screened, and scheduled efficiently while maintaining strict compliance with clinical research standards and protocols.

Responsibilities

• Support the conduct of a clinical trial focused on an RSV vaccine in accordance with study protocols and regulatory requirements.
• Perform detailed chart reviews using the electronic medical record (EMR) system to identify potential study participants who meet inclusion and exclusion criteria.
• Conduct pre-screening of potential participants, verifying eligibility based on medical history, current health status, and protocol-defined criteria.
• Coordinate and schedule patient appointments for study-related visits, ensuring that participants receive timely communication and clear instructions.
• Manage and document patient recruitment activities, tracking outreach, responses, and enrollment status in an organized and accurate manner.
• Collaborate with the research team to address patient eligibility questions and resolve issues related to scheduling or documentation.
• Maintain strict adherence to Good Clinical Practice (GCP) guidelines and HIPAA regulations throughout all aspects of patient recruitment and data handling.
• Ensure that all patient information and study records are handled confidentially and accurately within the EMR and study systems.
• Contribute to a fast-paced research environment by prioritizing tasks, meeting timelines, and maintaining a high level of attention to detail.

Essential Skills

• Minimum of 2 years of experience working as a Clinical Research Coordinator.
• Proven experience with patient recruitment in clinical research settings.
• Hands-on experience using electronic medical record (EMR) systems for chart review and documentation.
• Strong ability to perform detailed chart reviews to identify eligible study participants.
• Demonstrated experience with pre-screening patients for clinical trials.
• Training in HIPAA regulations and patient privacy requirements.
• Training in Good Clinical Practice (GCP) for clinical research.
• Ability to manage multiple tasks in a fast-paced clinical research environment with strong attention to detail.
• Effective communication and organizational skills to coordinate patient appointments and recruitment activities.

Additional Skills & Qualifications

• Experience working on vaccine or RSV-related clinical studies is an advantage.
• Comfort working within structured research protocols and standard operating procedures.
• Ability to collaborate effectively with investigators, clinical staff, and other research team members.

Job Type & Location

This is a Contract position based out of Norfolk, NE.

Pay and Benefits

The pay range for this position is $25.00 - $33.00/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)

Workplace Type

This is a fully onsite position in Norfolk,NE.

Application Deadline

This position is anticipated to close on Jun 19, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 actalentaccommodation@actalentservices.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.