Clinical Research Associate II / Sr. CRA

Rho

Clinical Research Associate monitoring pain studies for Rho, a contract research organization. Conducting site visits, managing clinical trial compliance, and keeping data audit ready across multiple protocols.

Posted 8/14/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $90,000 - $140,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in site monitoring activities, including PSV, SIV, IMV, and COV visits, while ensuring clinical trial data remains audit ready. Proficient in developing clinical trial protocols and maintaining effective relationships with clinical sites and teams.

Highest-signal resume keywords

Onsite Monitoring ExperienceClinical Trial Protocol DevelopmentEDC Systems ProficiencyStrong Written And Verbal CommunicationAttention To Detail

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site MonitoringClinical Trial Protocol DevelopmentMedical TerminologyData Audit ReadinessMonitoring Pain Studies

Soft Skills

Critical ThinkingProblem-SolvingCollaborationAgilityAdaptability

Tools & Technologies

Microsoft OfficeEDC Systems

Industry Keywords

CROPharmaceuticalBiotechnologyClinical OperationsRFP Process

About the role

Key responsibilities & impact

Perform all site monitoring visit activities, including PSV, SIV, IMV, and COV visits
Participate in site selection with oversight from the Clinical Team Lead
Provide feedback to sites on deficiencies and corrective actions, and follow up until resolution
Contribute to developing and reviewing clinical trial protocols, study tools, materials, and documentation
Mentor, train, and co-monitor junior clinical team members
Develop and maintain effective relationships with clinical sites and Rho teams
Communicate project goals and critical requirements
Attend and present at meetings and conferences, including Investigator Meetings
Participate in the RFP process and business development meetings
Contribute to Rho’s Clinical Operations community, internal initiatives, and standard operating procedures
Perform onsite and remote monitoring and study closure activities across multiple protocols
Conduct 8–10 site visit days per month, with up to 80% travel
Ensure clinical trial data remains audit ready and can pass audits by Rho, sponsors, or regulatory agencies

Requirements

What you’ll need

BA/BS, preferably in life science, nursing, pharmacy, or a related field
Approximately 2 years of onsite monitoring experience for CRA II or 4–5+ years for Senior CRA
Experience within the CRO, pharmaceutical, or biotechnology industry
Experience monitoring pain studies
Understanding of medical or therapeutic area knowledge and medical terminology
Computer literacy
Proficiency in Microsoft Office
Experience using EDC systems
Strong written, verbal, and presentation skills
Strong organization and attention to detail
Ability to manage multiple sites and protocols within timelines and budgets
Ability to work collaboratively with honesty and integrity
Critical thinking and practical problem-solving ability
Agility and adaptability
Must be located within a 1-hour commute of a US metropolitan airport
Ability and commitment to conduct 8–10 site visit days per month, with up to 80% travel

Benefits

Comp & perks

Medical, vision, and dental insurance
Health Savings Account (HSA)
Flexible Spending Account (FSA)
Employee Assistance Program (EAP)
Life and disability insurance
401(k)
Paid time off
Paid holidays
Parental leave
Bereavement leave
Work-life balance flexibility
Career growth opportunities
Financial rewards
Stable employment environment