Senior Clinical Research Associate – Oncology

Worldwide Clinical Trials

. Manage research activities at sites participating in Worldwide’s clinical research projects .

Posted 10/5/2026full-timeRemote • United StatesSenior💰 $97,000 - $193,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research activities, ensuring compliance with regulatory requirements, and effectively training site personnel. Proficient in utilizing CTMS and EDC systems while maintaining superior organizational and communication skills.

Highest-signal resume keywords

Clinical Research Associate ExperienceOncology ExperienceCTMS ProficiencyEDC Systems ProficiencyRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ManagementStudy Start-Up ActivitiesData Collection TrainingSafety-Event ReportingStudy Maintenance Management

Soft Skills

Interpersonal CommunicationOrganizational SkillsAttention to DetailAbility to Work Independently

Tools & Technologies

Microsoft OfficeCTMSEDC Systems

Certifications & Qualifications

4-Year University DegreeNursing Degree

Industry Keywords

Clinical ResearchInformed Consent ProceduresMidwest United StatesTravel Willingness

About the role

Key responsibilities & impact

Manage research activities at sites participating in Worldwide’s clinical research projects
Participate in all stages of clinical studies, including identifying potential sites
Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations
Train sites to collect data properly and report potential safety-related events
Manage site activities during study maintenance
Close down research activities at sites after study conclusion
Conduct study initiation visits (SIVs)
Ensure compliance with informed-consent procedures, safety-event reporting, and applicable regulatory requirements while performing remote site management

Requirements

What you’ll need

Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Experience in Oncology is required
Candidates must reside in the Midwest United States
Willingness to travel regionally required

Benefits

Comp & perks

Competitive benefits package depending on location
Professional development through regular touchpoints and coaching conversations with a Line Manager
Clear career path and development that can lead to Clinical Trial Manager roles
Supportive and team-oriented work environment
Inclusive and equitable workplace