Clinical Research Nurse

Clinical Research NurseThis Clinical Research Nurse role supports a nasal polyp clinical trial at a dedicated research site in Roseville, CA. You will contribute to all aspects of the clinical trial, from participant screening and recruitment to data collection and regulatory support. The position requires strong clinical research experience, excellent organizational skills, and confident communication with both participants and research staff. This is a full-time role at 40 hours per week.ResponsibilitiesReview electronic medical records (EMR) to assess potential participants against study inclusion and exclusion criteria.Pre-screen potential participants based on protocol-defined eligibility requirements.Recruit and enroll participants into the clinical trial in accordance with study protocols and regulatory requirements.Obtain informed consent from patients in compliance with ethical and regulatory standards.Collect and enter study data accurately into electronic data capture (EDC) systems.Verify data to ensure completeness, accuracy, and consistency with source documentation.Resolve data queries in collaboration with the study team and sponsors as needed.Provide regulatory support by following established procedures and maintaining required documentation.Collect and process biological specimens according to study protocols and safety guidelines.Measure and record vital signs and other clinical assessments as required by the protocol.Administer investigational products (IP) to patients in accordance with study procedures and safety requirements.Conduct chart reviews to confirm eligibility, document medical history, and track participant progress.Coordinate and support patient recruitment activities to meet enrollment goals.Collaborate closely with investigators, coordinators, and other research staff to ensure smooth study operations.Maintain a high level of attention to detail in all clinical and documentation activities within a fast-paced research environment.Essential SkillsMinimum of 2 years of experience working as a Clinical Research Nurse.Hands-on experience supporting clinical trials, including patient recruitment, pre-screening, and enrollment.Proficiency in reviewing and interpreting electronic medical records (EMR).Experience with electronic data capture (EDC) systems for data entry and management.Demonstrated ability to obtain informed consent and explain study procedures clearly to participants.Competence in data verification and query resolution to ensure high-quality clinical trial data.Training in Health Insurance Portability and Accountability (HIPAA).Training in Good Clinical Practice (GCP).Clinical skills including specimen collection and processing, and taking vital signs.Ability to administer investigational products (IP) safely and according to protocol.Strong organizational skills with the ability to manage multiple tasks in a fast-paced environment.Excellent verbal and written communication skills for interacting with participants and research staff.Attention to detail and accuracy in documentation and regulatory compliance.Additional Skills & QualificationsExperience working as a Clinical Research Coordinator or in a similar clinical research role.Experience in patient recruitment for clinical trials, including outreach and screening.Familiarity with regulatory processes and documentation in clinical research.Experience conducting chart reviews to support eligibility assessments and ongoing study documentation.Ability to build rapport with participants and support them throughout the study.Comfort working within multidisciplinary research teams and adapting to changing study needs.Work EnvironmentThis position operates within a clinical research site in Roseville, CA, supporting a nasal polyp clinical trial. The role follows normal business hours and is structured as a 40-hour work week. The environment is fast paced and requires a high level of attention to detail in all clinical, data, and regulatory activities. You will work regularly with electronic medical records (EMR) and electronic data capture (EDC) systems, as well as standard clinical equipment used for vital signs and specimen collection. The setting is professional and focused on delivering high-quality, compliant clinical research.Job Type & LocationThis is a Contract position based out of Roseville, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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)Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Roseville, CA.About ActalentActalent 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 click.appcast.io 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.