Clinical Research Associate

Kelly Services; Salt Lake City (UT); Remote; USD 77,000 - 85,000; Full time

Benefits offered by this job

Medical benefits

Retirement plan

Paid holidays

Transit benefit

Job summary

Kelly Science & Clinical is seeking a Clinical Research Associate I to support West Coast studies through remote or on-site monitoring, ensuring protocol and regulatory compliance and data integrity. You will coordinate documentation, site communications, and study-wide monitoring tasks while maintaining audit readiness.

Ideal candidates have 2+ years in clinical research monitoring, a life sciences degree or RN, strong ICH-GCP knowledge, and a willingness to travel regionally up to 80% as

Qualifications

• Bachelor's degree or RN and related qualification.
• 2+ years of clinical research monitoring experience.
• Experience with complex therapeutic areas; CRO background preferred.
• Valid driver’s license.

Responsibilities

• Site Monitoring & Compliance using risk-based monitoring to ensure protocol adherence.
• Data Integrity through SDR/SDV/CRF review.
• Documentation & reporting of observations in timely, professional manner.
• Issue escalation and CAPA tracking to resolution.
• Maintain/track trial status in CTMS and related systems.
• Support site relationships and investigator meetings as needed.

Skills

Clinical monitoring

Site management

Documentation

Regulatory compliance

Communication

ICH-GCP knowledge

RBM concepts

MS Office

CTMS familiarity

Remote monitoring

Education

Bachelor's degree in life sciences

RN certification

Tools

CTMS

MS Office

EDC systems

Job description

Clinical Research Associate I

• Location: Remote / Home office located near major cities in CA, NV, CO, UT, or AZ
• Travel: Regionally aligned for West Coast travel (up to 80% as needed)
• Employment Type: W-2 hourly, full-time contract (6 months with potential to extend )
• Pay Rate: $55.86 – $62.07/hour door-to-door (limited benefits options available)

Summarized Purpose

Kelly Science and Clinical is hiring on behalf of one of our large CRO clients to support a six-month project with the potential for future extension. We are looking for strong CRA monitors to support regional studies at sites across the West Coast. Ideal candidates will have at least two years of experience monitoring complex therapeutic studies, with prior large CRO experience preferred. The CRA I performs and coordinates all aspects of the clinical monitoring and site management process. This role conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation across various monitoring environments (e.g., FSO, FSP, Government). As a site processes specialist, the CRA I ensures trials are conducted in accordance with approved protocols, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability while maintaining audit readiness. The CRA I develops collaborative relationships with investigational sites and project team members. Detailed tasks and responsibilities are outlined in the project task matrix.

Essential Functions

• Site Monitoring & Compliance: Monitors investigator sites using a risk-based monitoring approach; applies root cause analysis (RCA), critical thinking, and problem-solving skills to identify site process failures and implement corrective/preventive actions (CAPA) to bring sites into compliance.
• Data Integrity: Ensures data accuracy through Source Document Review (SDR), Source Document Verification (SDV), and Case Report Form (CRF) review during on-site and remote monitoring activities.
• IP Management: Assesses investigational products through physical inventory checks and records reviews.
• Documentation & Reporting: Documents observations in reports and follow-up letters in a timely manner using professional business writing standards.
• Issue Escalation: Escalates observed deficiencies to clinical management expeditiously and follows all issues through to resolution.
• Site Relations & Follow-Up: Maintains regular contact with investigative sites between visits to confirm protocol adherence, track issue resolution, and ensure timely data entry.
• Trial Execution: Conducts monitoring tasks in accordance with the approved monitoring plan, assists with the investigator payment process, and participates in investigator meetings as needed.
• Tracking & Systems: Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM). Updates study systems (e.g., CTMS) per agreed study conventions and performs QC checks on CTMS-generated reports as required.
• Site Selection & Initiation: Collaborates with the client company to identify qualified investigators, initiates clinical trial sites according to relevant procedures, and makes recommendations as warranted.
• Study Close-Out: Oversees trial close-out procedures and the retrieval of trial materials.
• Regulatory & Essential Documents: Ensures required essential documents are complete, accurate, and filed according to ICH-GCP guidelines and applicable regulations. Conducts on-site file reviews per project specifications.
• Team Contribution: Contributes to the project team by assisting in the preparation of project publications and tools, as well as sharing actionable ideas and suggestions with team members.
• Study Tasks & Leadership: Performs additional study tasks assigned by the CTM, such as trip report reviews, newsletter creation, and leading CRA team calls.
• Stakeholder Communication: Facilitates effective communication between investigative sites, the client company, and the project team through written, oral, and electronic channels.
• Audits & Quality Assurance: Responds to company, client, and applicable regulatory requirements, audits, and inspections.
• Administrative: Completes administrative tasks, including expense reports and timesheets, in a timely manner.
• Process Improvement: Contributes to project initiatives and process improvement efforts as required.

Education and Experience

• Bachelor's degree in a life science-related field, a Registered Nurse (RN) certification, or equivalent relevant academic/vocational qualification.
• 2+ years of experience as a clinical research monitor or equivalent experience demonstrating the necessary knowledge, skills, and abilities.
• Prior monitoring experience complex therapeutic areas, with large CRO experience preferred.
• Valid driver's license.

Knowledge, Skills, and Abilities

• Effective clinical monitoring skills across full study lifecycles.
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology.
• Strong understanding and practical application of ICH-GCP guidelines, applicable regulations, and procedural documents.
• Well-developed critical thinking skills, including root cause analysis (RCA) and proactive problem-solving.
• Ability to apply Risk-Based Monitoring (RBM) concepts and processes.
• Clear oral and written communication skills with the ability to interact effectively with medical personnel and site staff.
• Strong customer focus with active listening skills, high attention to detail, and the ability to address underlying customer needs.
• Excellent interpersonal, organizational, and time-management skills.
• Ability to remain flexible and adaptable across a range of study scenarios.
• Proven ability to work effectively both independently and as part of a collaborative team.
• Computer proficiency, including Microsoft Office applications, with the ability to quickly learn EDC and CTMS platforms.
• Strong English language and grammar skills.
• Effective presentation and communication skills.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (https://www.mykelly.com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice (https://www.kellyservices.com/hubfs/myKelly/Resources/Employment_Policies/Recruitment-Artificial-Intelligence-Notice.pdf?hsLang=en) .

Kelly Services is proud to be an Equal Employment Opportunity and affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.