Senior Clinical Research Associate – Oncology

Worldwide Clinical Trials

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

Posted 9/17/2026full-timeRemote • Minnesota • 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 data collection and safety-event reporting within the Oncology domain.

Highest-signal resume keywords

Clinical Research Associate ExperienceOncology ExperienceMicrosoft Office ProficiencyCTMS ProficiencyEDC Systems Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study Start-Up ActivitiesRegulatory Document CollectionContract NegotiationData Collection TrainingSafety-Event ReportingStudy Maintenance ManagementStudy Initiation Visits

Soft Skills

Interpersonal CommunicationOral CommunicationWritten CommunicationOrganizational SkillsAttention to Detail

Certifications & Qualifications

4-Year University DegreeNursing Degree

Industry Keywords

Clinical ResearchInformed-Consent ProceduresRegulatory ComplianceCentral United States ResidencyRegional Travel Willingness

About the role

Key responsibilities & impact

Manage research activities at sites participating in Worldwide’s clinical research projects
Identify potential sites to participate in research
Perform study start-up activities, including collecting regulatory documents from sites
Support negotiation of contracts and budgets
Train sites to collect data properly and report potential safety-related events
Manage site activities during study maintenance
Close down research activities at sites once the study has concluded
Conduct study initiation visits (SIVs)
Ensure compliance with informed-consent procedures, safety-event reporting, and applicable regulatory requirements

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 required
Candidates must reside in the Central United States
Willingness to travel regionally required

Benefits

Comp & perks

Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
Regular touchpoints and coaching conversations with Line Manager
Clear career path and professional development leading to Clinical Trial Manager roles
Accessible Executive Leadership team
Competitive benefits package depending on location