** 외국계CRO 다직종 채용
Position | Main role | Qualifications |
BDA | - 견적서 작성 및 계약서 진행 업무 - 신규 클라이언트 개발 및 방문 - 입찰 프로젝트 진행 및 프레젠테이션 등 | - 전공: 자연계열 인문계열 전공 및 의료/보건관련 - 경력: 2~6년 업무 경력자(사무직, 영업 관리직 등) (CRO 혹은 제약사 업무 경력자, 임상시험/의료/보건 업계 관련 종사자, 마케팅 관련 업무 경험자 선호) - 요구 능력(필수): 비즈니스 이메일 작성 가능자, Business English, Excel/PPT/Word문서작업능력 중상, 프레젠테이션 발표능력 |
CRA | - 국내 및 해외 임상시험 - Monitoring, Site management | - 학력: 간호학 및 관련 전공자 - CRO에서 CRA 경력 2년 이상(전기 경험 필수) - Oncology 경력자 우대 - 영어 가능자 - Interpersonal skill 우수자 우대 |
Sr. Biostatistician | - 임상 관련 통계 업무 - SAS 프로그램을 이용한 임상 통계 분석 (SAP 작성 및 SAS Programming, CDISD ADaM 생성 등) - 대상자 수(sample size) 산출 및 무작위배정 코드 생성 등 | - 학력: 통계, 임상통계 전공 석사 이상 - 경력: 3~4년 이상 - 임상 자료 분석 경험 우대 - 영어 우수자 우대 - 제약회사 및 CRO 관련 분야 경력자 우대 |
CPM (Early Phase Study) | - Overall project managementevery aspect to ensure all deliverable are met and client is satisfied with the service delivery and results - Support in operations and/or business’s continuity by undertaking tasks such as: : Mentoring and training of new employees as required : Support and participate in business development activities : Review, revise and/or develop Project Management related SOPs, work guides etc : Ensure sales target and profitability of CAS local office : Resource management and cost-efficiency within CAS local office : Support business related work designated by Company | - CRO 경력 최소 2년 이상 필수 - Global CRO FIH 1~2상 PM 경력자 우대, - Regionalglobal projects experience in Global CRO경험 우대 - 영어 능통자 (논의/토론 가능한 수준) - 경력에 따라 직급 부여 (CPM I, II, Senior) *Competitive Salary Package 제공 예정 *PM포지션 풀재택 조율 가능 |
Project Director | 1. Lead, supervise, execute, manage and monitor daily business operations and service performance to achieve financial goals and business growth objectives of responsible operations; PMs (including CPA(s) and CPS(s)) in Korea 2. Responsible for overseeing a number of Projects to ensure that all deliverablesthe program are met and that the client is satisfied with the service delivery and results. 3. Responsible for the quality check of scientific documents according to the international medical and scientific document standards (e.g., ICH guidelines). Documents include Clinical Study Protocol, Informed Consent Form (ICF), Clinical Study Report (CSR), Post Marketing Surveillance (PMS) documentspublication manuscripts, etc. 4. Lead, manage and supervise in hiring, onboarding, performance evaluation, resourcing, talent retention and succession planning processes of PM department. Ensure appropriate utilization and delivery resource supply/demand balancing inclusive of talent attraction, talent placement, on-boarding and training within responsible operation functions; PMs (including CPA(s) and CPS(s)) 5. Collaborate with stakeholders to develop, establish, execute, manage and supervise service quality standards and performance deliverables to ensure all policies, procedures, standards, specifications, guidelines, training programs and cultural values are in line with Company Group and CRO business unit. Champion and support the development and implementation of Quality Management System and GxP processes to lift up operations standards and performance excellence. 6. Oversee day-to-day operations, review tasks execution and performance status, and report to supervisor on matters related to Operations and Quality 7. Guide, resolve and improve internal and external conflicts, complaints and underperformance efficiently and to the mutual benefit of those involved. Ensure corrective and preventive actions are executed fully and timely 8. Collaborate with Company stakeholders to provide insights, recommendations, and assistance to develop strategies and operational plans towards continued business growth and profitability 9. Guard, control, carry out costs savings measures and develop improvement actions to meetexceed budgetary and agreed performance targets to create a sustainable organization 10. Have a primary responsibility to manage PM resource and conduct regular 1:1 sessions with direct reports and the team meeting, identify areas for development and ensure that all trainings are effective and meeting the training and personal development objectives. Lead, act and supervise the implementation of trainings to ensure professional development and career advancement of the employees within responsible business operations 11. Take a responsibility to lead portfolio/ project as per resource availability in Korea 12. Demonstrate leadership by examples to create a stimulating, positive, energetic work atmosphere by adopting CAS “FOCUS Principles” with “CARE” ? Communication, Appreciation, Respect and Empathy to foster a happy, harmony, caring and healthy workplace 13. Keep abreast of competitive regulatory and clinical practices and utilize such knowledge for continuous improvements. Understand evolving customer strategy and industry trends and how that changes may impact Company future service delivery needs. Ensure service offerings evolve in line with/ahead of customer evolving needs and expectations. 14. Respond to routine and non-routine inquiries and assignments in a timely and professional manner by the company 15. Support and lead business development activities as assigned | - Minimum bachelor degree (major in nursing, pharmacyother bio-science-related background)a recognized institution, and/or equivalent combination of training and experience - Minimum 13 years’ experience in clinical research in healthcare, pharmaceutical and/or CRO industry,relevant experience - minimum 5 years direct experience as clinical project manager in multi-national clinical trials and/or ICCC trials - Preferred to have at least 2 years of PM experience in Global CROs -Good understanding of cross-functional processes, clinical trial processes and the regulatory environment -Good organizational, leadership, negotiation and interpersonal skills -Excellent |
** 이메일
- sgchung20021@hanmail.net (영문CV)
- 프로핸즈코리아 정수길부사장 010-6566-6370
- ASAP
3. Responsible
4. Lead, manage
5. Collaborate with stakeholders to develop, establish, assigned
- Minimum bachelor