한국 MSD의 임상부서인 GCTO팀에서 CRA로 근무해주실분을 다수 모집합니다.

지원자격은Global monitoring 경력이 있으신 분(Oncology study 선호)입니다. (최소 1년 5개월의 경력 요구)
관련하여 궁금한 점이 있으신 분들께서는 kr_recruit@merck.com 으로 문의 주십시오. 지원 방법은 하단의 내용 확인 부탁드립니다.. 

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.

•Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.

•Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.

•Gains an in-depth understanding of the study protocol and related procedures.

•Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.

•Participates & provides inputs on site selection and validation activities.

•Performs remote and on-site monitoring & oversight activities using various tools to ensure:

o Data generated at site are complete, accurate and unbiased

o Subjects’ right, safety and well-being are protected

•Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.

•Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.

•Communicates with Investigators and site staff on issues related to protocol conduct,

recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.

•Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRM, PLM and RCPM.

•Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.

•Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required.

•Supports and/or leads audit/inspection activities as needed

Competency Expectations:

•Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively.

•Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

•Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.

•Hands on knowledge of Good Documentation Practices

•Proven Skills in Site Management including management of site performance and patient recruitment

•Demonstrated high level of monitoring skill with independent professional judgment.

•Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices.

•Ability to understand and analyze data/metrics and act appropriately

Behavioral Competency Expectations:

•Effective time management, organizational and interpersonal skills, conflict management, problem solving skills

•Able to work highly independently across multiple protocols, sites and therapy areas.

•High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.

•Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.

•Demonstrates commitment to Customer focus.

•Works with high quality and compliance mindset