Oncology Specialist
PSI CRO
Escondido, CA
oncology
medical
research
safety
psi
clinical research
oncology
team
project teams
regulatory
clinical development
reputation
business partners
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April 6, 2025
PSI CRO
Escondido, CA
FULL_TIME
At PSI CRO, we're dedicated to pushing the boundaries of clinical research services. With 30 years of experience, we've established a reputation for finding that perfect balance between stability and innovation.
We're looking for an exceptional Oncology Specialist to join our team. In this role, you'll provide crucial medical input to global clinical studies, working closely with project teams, regulatory agencies, and business partners to ensure patient safety and well-being.
Main Responsibilities:
• Offer expert medical advice to clients, project teams, sites, and third-party vendors
• Collaborate in the development of clinical development plans, protocols, and scientific presentations
• Ensure the accuracy and completeness of reported data, adhering to regulatory guidelines
• Address safety concerns throughout the study, reviewing listings for coded events
• Participate in bid defense meetings and support Pharmacovigilance activities
• Identify program risks and create mitigation strategies with Clinical Operations
• Lead clinical development advisory boards and safety monitoring boards
• Review and approve clinical documents, ensuring medical relevance
Necessary Qualifications:
• MD degree required
• Board certification in Oncology essential
• At least 10 years of experience as a practicing Oncologist
• Clinical research experience, including PI or SI roles
• Full working proficiency in English
• Proficiency with MS Office applications
• Excellent communication, presentation, and public speaking skills
• Problem-solving, teamwork, and attention to detail
This role offers an excellent opportunity to join PSI CRO's global team of medical professionals, contribute to innovative research, and make a real difference in patients' lives.
We're looking for an exceptional Oncology Specialist to join our team. In this role, you'll provide crucial medical input to global clinical studies, working closely with project teams, regulatory agencies, and business partners to ensure patient safety and well-being.
Main Responsibilities:
• Offer expert medical advice to clients, project teams, sites, and third-party vendors
• Collaborate in the development of clinical development plans, protocols, and scientific presentations
• Ensure the accuracy and completeness of reported data, adhering to regulatory guidelines
• Address safety concerns throughout the study, reviewing listings for coded events
• Participate in bid defense meetings and support Pharmacovigilance activities
• Identify program risks and create mitigation strategies with Clinical Operations
• Lead clinical development advisory boards and safety monitoring boards
• Review and approve clinical documents, ensuring medical relevance
Necessary Qualifications:
• MD degree required
• Board certification in Oncology essential
• At least 10 years of experience as a practicing Oncologist
• Clinical research experience, including PI or SI roles
• Full working proficiency in English
• Proficiency with MS Office applications
• Excellent communication, presentation, and public speaking skills
• Problem-solving, teamwork, and attention to detail
This role offers an excellent opportunity to join PSI CRO's global team of medical professionals, contribute to innovative research, and make a real difference in patients' lives.
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