Remote Oncology Clinical Research Associate II

HiRO - Harvest Integrated Research Organization; Nevada (IA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Remote work with travel

Job summary

Harvest Integrated Research Organization (HiRO) is seeking a Clinical Research Associate II to monitor and manage Phase I–IV trials. This remote role involves site visits and frequent travel to ensure protocol adherence, GCP/ICH compliance, and data integrity across assigned sites.

The CRA II will support patient recruitment, site logistics, and audit readiness, collaborating with sponsors and teams to meet timelines and deliverables. Oncology monitoring experience is required.

Qualifications

• Minimum 2 years of independent monitoring experience.
• Excellent oral and written communication skills in English, including proficient presentation skills.
• Oncology monitoring experience required.
• Excellent communication, collaboration, and problem-solving skills.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Demonstrate good computer skills and be able to embrace new technologies.
• Ability to manage travel up to 75% on a regular basis, including air travel.

Responsibilities

• Performs on-site site qualification, initiation, interim monitoring, site management and close-out visits with regulatory and protocol compliance.
• Verifies informed consent processes and documentation.
• Assesses site processes and conducts Source Document Review of site records.
• Verifies data entry in CRFs and ensures accuracy.
• Resolves data queries remotely and on-site, guiding site staff to closure.
• Uses hardware/software to support data review and capture for the project.

Skills

English communication

Presentation skills

Excellent written communication

Travel readiness

Independent monitoring experience

Problem-solving

Education

Bachelor’s degree or RN in a related field

Job description

Harvest Integrated Research Organization (HiRO) is seeking a Clinical Research Associate II to monitor and manage Phase I–IV trials. This remote role involves site visits and frequent travel to ensure protocol adherence, GCP/ICH compliance, and data integrity across assigned sites.

The CRA II will support patient recruitment, site logistics, and audit readiness, collaborating with sponsors and teams to meet timelines and deliverables. Oncology monitoring experience is required.