Clinical Research Associate – CRA II/Senior

Parexel

. Manage clinical sites from identification through closeout .

Posted 10/2/2026full-timeRemote • United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical sites throughout the study lifecycle, ensuring compliance with Good Clinical Practice and regulatory requirements while fostering strong relationships with site teams and investigators. Proficient in utilizing Clinical Trial Management Systems and Electronic Document Management Systems to support study execution and data integrity.

Highest-signal resume keywords

Clinical Research Associate ExperienceOncology Clinical Trial MonitoringGood Clinical Practice KnowledgeClinical Trial Management System ProficiencySite Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Onsite MonitoringData Quality EvaluationSite Document VerificationPatient Recruitment StrategiesRegulatory Documentation Monitoring

Soft Skills

Problem-SolvingCommunicationInterpersonal SkillsOrganizational SkillsAttention to Detail

Tools & Technologies

Clinical Trial Management SystemElectronic Document Management SystemMicrosoft OfficeExcelWord

Industry Keywords

Clinical TrialsRegulatory RequirementsGood Clinical PracticeStudy ProtocolsPatient-Focused Approach

About the role

Key responsibilities & impact

Manage clinical sites from identification through closeout
Serve as the primary point of contact for assigned clinical site teams
Conduct qualification visits, site initiation visits, monitoring visits, and termination visits
Prepare timely visit and contact reports
Manage site quality and delivery throughout the study lifecycle
Address site questions and resolve issues to support study execution
Oversee study integrity and build relationships with investigators and site staff
Review trial performance and safeguard participant rights, safety, and well-being
Develop patient recruitment strategies with clinical sites to support enrollment timelines
Ensure compliance with SOPs, study protocols and amendments, Good Clinical Practice, and regulatory requirements
Evaluate reported data quality and integrity, site performance, and investigational product accountability
Monitor regulatory documentation completeness and quality
Perform site document verification
Conduct onsite monitoring activities and support enrollment and study delivery

Requirements

What you’ll need

At least 18 months of direct onsite monitoring experience as a Clinical Research Associate
Oncology, Ophthalmology, Metabolic, Hematology or CAR-T clinical trial monitoring experience required
Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline
Knowledge of Good Clinical Practice, applicable regulatory requirements, and clinical trial processes
Experience using a Clinical Trial Management System, an Electronic Document Management System, and Microsoft Office applications, including Excel and Word
Strong site relationship management, problem-solving, communication, interpersonal, written, verbal, organizational, and attention-to-detail skills
Ability to work independently with urgency and limited oversight
Ability to manage multiple priorities, evaluate changing scenarios, apply study protocols, and meet project timelines
Ability to collaborate within a matrixed team and communicate clearly with internal and external stakeholders
Ethical, patient-focused approach
Client-focused, flexible approach to assignments and continuous learning

Benefits

Comp & perks

Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
Paid time off
Life insurance
Additional benefit offerings in accordance with applicable plan terms
Potential eligibility for additional incentives, bonuses, or other compensation programs