Senior Clinical Research Associate
PSI CRO AG
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇦🇷 Argentina
Visit company websiteJob Level
Senior
About the role
- Training, mentoring and supervising study level responsibilities for Jr. CRAs
- Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
- Delivering training of investigators, site staff and project teams
- Work with complex studies
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be involved in site identification process
- Contact for clinical investigators, vendors and support services in regard to study progress
- Participate in feasibility research
- Preparation and delivering of presentations at Investigator’s Meetings
- Preparation for and attendance at company’s audits; resolution of audit findings
- Support to Regulatory Affairs in procurement of site regulatory documents
- Maintenance of study-specific automated tracking systems
Requirements
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Full working proficiency in Spanish and English
- At least 3 years of independent on-site monitoring experience in Argentina
- Experience in all types of monitoring visits in Phase II and/or III
- Availability to travel
- Experience in Oncology or Infectious Diseases is a plus
- Proficiency in MS Office applications
- Ability to plan and work in a dynamic team environment
Benefits
- Professional development
- Tailored courses and mentoring
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
CRF reviewsource document verificationquery resolutionmonitoring visitsfeasibility researchstudy-specific automated tracking systemsOncologyInfectious Diseases
Soft skills
trainingmentoringsupervisingcommunicationplanningteamwork
Certifications
College/University degree in Life Sciences