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Senior Clinical Research Associate – Oncology
LifelancerSenior Clinical Research Associate managing site activities in Oncology clinical studies. Collaborating with teams for effective patient data collection and compliance in the Central U.S.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in managing clinical research activities, ensuring compliance with regulatory requirements, and obtaining informed consent. Proficient in site management and has a strong background in Oncology.
Highest-signal resume keywords
Clinical Research Associate ExperienceOncology ExpertiseRegulatory ComplianceSite ManagementInformed Consent
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Study ManagementSite IdentificationStudy Initiation VisitsData CollectionProtocol Adherence
Soft Skills
CommunicationOrganizational SkillsProblem-Solving
Certifications & Qualifications
4-Year University DegreeNursing Degree
Industry Keywords
Clinical ResearchOncologyInformed ConsentRegulatory RequirementsCentral United States
About the role
Key responsibilities & impact- Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
- Typically involved in all stages of the clinical study, including identifying potential sites, conducting study initiation visits, and managing site activities
- Ensure compliance with obtaining informed consent and adhering to regulatory requirements
Requirements
What you’ll need- 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 Central United States
- Willingness to travel regionally required
Benefits
Comp & perks- Competitive benefits package depending on location
- Pay equity and transparency