대한민국.의 Parexel 채용 정보

This role involves leading study-level site contracting activities, guiding other contract leads, and serving as the primary contact for site contracting issues and timelines on assigned studies. · ...

IND, NDA, 임상시험 승인계획 신청, 품목허가(변경)신청 및 관리 등, 최소 3년 이상의 RA 업무 경험자 (국내 허가관련 업무의 경력자) · Chemistry, Biology, Pharmacy 혹은 그 외 유관 전공 학사 이상 · Parexel 오피스/ 재택 근무 병행 (풀재택 수준) · Key Accountabilities · Project Execution: · Works effectively within a team environment but may work independentl ...

FSP team manager 채용 · FSP LM 경험자 (최소 2-3년 이상) · CRA 경험 포함 8-10년 이상 경력자 · Key Accountabilities · Project Delivery Management and Oversight · Monitor performance by close interaction with project leadership/functional leadership and ensure that ongoing/revised project documentatio ...

Clinical Research Associate role involves working with sites to ensure timely and accurate completion of project goals. · ...

The Real-World Data (RWD) Intern will support the Scientific Data Strategy team's work, assisting in the identification and management of real-world data sources to provide data support for clinical research. · Data Source Identification and Assessment · Data Knowledge Management ...

Senior Regulatory Affairs Associate IND NDA clinical trial approval plan application product license change and management etc minimum 3 years of RA work experience (domestic permit related work experience) · Works effectively within a team environment but may work independently ...

We all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. · ...

Key Accountabilities · Contracting Deliverables · Exercise sound judgment in balancing client risk with clinical trial timeline impacts when making budget and contractual decisions · ...

Lead study-level site contracting activities guide other contract leads and serve as the primary contact for site contracting issues and timelines on assigned studies. · ...

IND, NDA, 임상시험 승인계획 신청, 품목허가(변경)신청 및 관리 등, 최소 3년 이상의 RA 업무 경험자 (국내 허가관련 업무의 경력자) · Chemistry, Biology, Pharmacy 혹은 그 외 유관 전공 학사 이상 · Parexel 오피스/ 재택 근무 병행 (풀재택 수준) · Key Accountabilities · Project Execution: · Works effectively within a team environment but may work independently ...

The Real-World Data (RWD) Intern will support the Scientific Data Strategy team's work. · ...

We all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, · and market access, every clinical development solution we provide is underpinned by something special - · a deep conviction in what we do.Act as Parexel's direct point o ...

When our values align, there's no limit to what we can achieve. · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something ...

When our values align, there's no limit to what we can achieve. · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something ...

The Clinical Trial Manager is responsible for the trial activities for responsible R/OPU. · This includes verifying the trial is conducted in compliance with GCP-ICH, local/global regulations, · application SOPs and according to the trial protocol by overseeing CRO and internal t ...