1. ÀÇ·Ú»ç: ¼¼°èÀûÀÎ À¯¸í CRO
2. ¸ðÁý ³»¿ë : ¿Ü±¹°è,Clinical Project Manager (°úÀå~ºÎÀå±Þ) ¸ðÁý
¢Ã Job Responsibilities(Á¤±ÔÁ÷) : °úÀå~ ºÎÀå±Þ 2,3¸í ä¿ë ¿¹Á¤
- Bachelor's degree in a health care or other scientific discipline or educational equivalent; 5 years clinical monitoring and one year in a project leadership role ; or equivalent combination of education, training and experience
- Establish appropriate clinical tools and processes for the study team to support the execution of clinical deliverable and study timelines.
- Manage clinical study set-up and follow-up study activities through ongoing tracking and review of study progress. Report progress to appropriate clinical management and project management forums.
- Collaborate with other functional groups within the company such as data management, pharmacovigilance, and biostatistics where necessary to support milestone achievement and to manager study issues and obstacles.
- Provide ongoing training and support to the clinical team. Establish study tools and training materials. Conduct frequent team meetings and ensure regular communication.
- Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring
/accompanied site visits and ongoing mentoring of CRA team.
- Develop the risk management plan from a clinical perspective and coordinate clinical issue escalation and resolution
- Identify quality issues within the study through regular review of the clinical team communications including site communications, monitoring visit reports, data flow information and quality assurance audit findings. Implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.
- Track clinical budget consumption through regular review of project budget reports.
- Establish customer service relationship with applicable client representative(s) as appropriate.
- May conduct monitoring visits at assigned sites for protocols that are complex and/or require knowledge in advanced therapeutic areas. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
¢Ã ¿¬ºÀ¼öÁØ ¹× º¹¸®ÈÄ»ý: Çö, ¿¬ºÀÀÌ»óÀ¸·Î ÃßÈÄ ÇùÀÇ °¡´É/ ÁÖ5ÀÏÁ¦
¢Ã ±Ù¹«Áö : ¼¿ï
¢Ã Á¦Ãâ¼·ù: ±¹,¿µ¹® À̷¼ ¹× »ó¼¼ °æ·Â±â¼ú¼¿Í Àڱ⠼Ұ³¼
¢Ã ÁøÇàÀýÂ÷ : 1Â÷ ¼·ù ÀüÇü- 2Â÷ ¸éÁ¢ÀüÇü
¢Ã ´ã´çÀÚ: °ûÁöÇý
¿¬¶ôó : 02-567-7407,7408
À̸ÞÀÏ : yskim@jhhr.co.kr
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