CRA - Monitor Texas

System One, Inc.; Grand Prairie (TX); On-site; USD 52,000 - 68,000; Part time

Benefits offered by this job

Health and welfare benefits

Job summary

System One is seeking a Contract/Part-time Clinical Research Associate (CRA) to monitor oncology trials in Texas with a flexible schedule starting at 20 hours per week. The role involves onsite and remote monitoring to ensure data integrity and patient safety, with travel to sites as required and a focus on regulatory compliance.

The candidate should have oncology monitoring experience, a healthcare background, and the ability to work independently. SOCRA or ACRP certification is preferred.

Qualifications

• Strong healthcare background with college degree or nursing certification.
• Proven ability to work independently and proactively.
• Excellent communication and problem-solving skills.
• Experience in oncology monitoring preferred.
• Familiarity with regulatory requirements (ICH/GCP) is a plus.

Responsibilities

• Site management to ensure study qualifications are met.
• Monitor assigned sites per monitoring plans.
• Ensure timely data submission and query resolution.
• Conduct onsite and remote monitoring activities.
• Maintain data integrity and patient safety per protocol.

Skills

Healthcare background

Communication

Autonomous work

Education

College degree or nursing certification

Tools

Medidata RAVE

Job description

Job Title: CRA - Monitor

Location: Texas

Type: Contract/Part time

We are seeking a dedicated Contract Clinical Research Associate (CRA) to join our team on a part-time basis. The role involves monitoring clinical trials within Texas, with a flexible schedule starting at a minimum of 20 hours per week, and potentially more depending on project needs. The ideal candidate will have experience in clinical trial monitoring within oncology and work independently to ensure study compliance and data integrity.

Responsibilities

• General site management, including ensuring sites meet study qualifications
• Monitoring of assigned study sites according to monitoring plans
• Ensuring timely data submission and query resolution
• Conducting continuous monitoring activities (onsite and remote)
• Implementing site management activities to ensure compliance with protocol, GCP, and regulations to secure data integrity and patient safety
• Acting as frontline liaison for Sponsor and sites to facilitate successful collaboration
• Responding to site questions and preparing reports
• Participating in calls and meetings as part of the study team
• Traveling approximately 60% of the time, with a valid driver’s license required

Requirements

• Strong healthcare background with a college degree or certification from an accredited school of nursing
• Minimum of five years oncology monitoring experience, particularly in hematology, multiple myeloma, and small cell lung cancer studies
• Knowledge of ICH, GCP, safety, and other regulatory requirements
• Professionalism, excellent planning, and autonomous work capability
• Good communication, problem-solving, and trend identification skills
• Computer proficiency, familiar with data management systems such as Medidata RAVE
• Certification from SOCRA or ACRP preferred

System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#LI-EL1
Ref: #568-Clinical