• Medical and safety monitoring and data review
• Develop, review, and revise protocols, CRF, training materials, code/data tables, listing and figures
• Actively participates and assists in preparations for investigator meetings
• Participates in project risk assessment activities
• Provides clinical and medical expertise to other Covance departments
• Contributes to the scientific strategic leadership for a given therapeutic area
• Partner with sales and support business development efforts; bid defence meetings, conferences, etc
경력 및 자격요건
• MD degree covering Oncology/Hemotology therapeutic areas
• Board Certification history
• Relevant sub specialty fellowship training
• Excellent communication and interpersonal skills
• 5+ years medical safety monitoring experience
• Clinical research experience with a CRO or Pharmaceutical
• Experience supporting Phase I - III clinical trials
• Strong knowledge and experience with Oncology/Hemotology clinical trials
• Previous experience in medical practice/patient care
• Experience attending and presenting at bid defence meetings
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
담당업무
입사지원
돌아가기
02-6281-5013
kimkt@nterway.com
