FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Senior Clinical Research Associate
PSI CRO AG. Conduct and report SIV, RMV, and COV onsite monitoring visits .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting onsite monitoring visits, including SIV, RMV, and COV, while effectively managing site relationships and communication. Proficient in regulatory document preparation and capable of supporting audits and inspections.
Highest-signal resume keywords
On-Site Monitoring ExperiencePhase II And III MonitoringRegulatory Document PreparationCommunication SkillsProficiency In MS Office
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
CRF ReviewSource Document VerificationQuery ResolutionFeasibility ResearchAudit ParticipationOncology Experience
Soft Skills
CommunicationCollaborationProblem-SolvingMultitaskingTeamwork
Industry Keywords
Life SciencesClinical ResearchStudy SubmissionsMonitoring VisitsDynamic Team Environment
About the role
Key responsibilities & impact- Conduct and report SIV, RMV, and COV onsite monitoring visits
- Perform CRF review, source document verification, and query resolution
- Manage site communication and site relationships
- Serve as a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support the regulatory team in preparing documents for study submissions
- Prepare for and participate in audits and inspections
Requirements
What you’ll need- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology is a plus
- Full working proficiency in English
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
- Must not require work visa sponsorship for employment now or in the future
Benefits
Comp & perks- Remote work available
- Opportunity to further develop skills
- Opportunity to widen therapeutic area experience
- Opportunity to become an expert in clinical research