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Senior Clinical Research Associate II
PfizerSenior Clinical Research Associate II managing complex investigator relationships and ensuring clinical quality at Pfizer. Leading monitoring community with responsibilities in global initiatives and regulatory audits.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research site monitoring, ensuring compliance with GCP, local laws, and Pfizer standards. Proven ability to lead teams, manage regulatory inspections, and enhance stakeholder engagement in the clinical trial process.
Highest-signal resume keywords
Clinical Research Site MonitoringGCP ComplianceOncology ExperienceRegulatory Inspection ManagementFluency in English
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial ManagementSite Care Partner DutiesStrategic Process ImprovementAudit Observation CAPA DevelopmentOnsite Monitoring ActivitiesRemote Monitoring ActivitiesCo-Monitoring ActivitiesHealth Care Professional EngagementLife Sciences DegreeNursing or Pharmacy Degree
Soft Skills
LeadershipMotivationTeam AlignmentCommunication
Industry Keywords
Clinical ResearchInvestigator SitesGlobal Clinical TrialsLocal LawsPfizer Standards
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Ensure superior clinical conduct across assigned investigator sites in accordance with Study Monitoring Plans, GCP, local laws, and Pfizer standards.
- Lead, motivate, and align the monitoring community.
- Perform the duties of a Site Care Partner (SCP) for small projects.
- Participate in or lead global, regional, or local working groups and strategic process improvement initiatives.
- Lead site preparation and serve as a central point of contact for regulatory inspections, audits, and Audit Observation CAPA developments.
- Conduct onsite, remote, and co-monitoring activities.
- Interface directly with health care professionals to enhance Pfizer's credibility.
Requirements
What you’ll need- Bachelor’s degree in Life Sciences or a professional degree in nursing, pharmacy, medical background, or equivalent.
- Minimum of 5 years of relevant experience in clinical research site monitoring (with a preference for 3 years of experience in Oncology).
- Prior global clinical trial experience is required.
- Fluency in English and the native language(s) of the country you will work in.
Benefits
Comp & perks- Health insurance
- Professional development opportunities
- Flexible working hours
- Paid time off
- Significant travel opportunities