Clinical Research Coordinator

GroupClinical Trials Unit (CTU)LocationThis post is based in Ha Noi, with some travel required.Hours of workFull time: Monday - Friday, 37.5 hours per week, extra hours may be requiredTenureInitially for 01 year, including a 02- month probation period, with possibility of extension based on annual performance appraisalReporting toCTU ManagerVacancy...

Mô tả công việc:(Mức lương: Thỏa thuận)Mô tả Công việcGroupClinical Trials Unit (CTU)LocationThis post is based in Ha Noi, with some travel required.Hours of workFull time: Monday - Friday, 37.5 hours per week, extra hours may be requiredTenureInitially for 01 year, including a 02-month probation period, with possibility of extension...

Group Clinical Trials Unit (CTU) Location This post is based in Ha Noi, with some travel required. Hours of work Full time: Monday - Friday, 37.5 hours per week, extra hours may be required Tenure Initially for 01 year, including a 02- month probation period, with possibility of extension based on annual performance appraisal Reporting to CTU Manager Vacancy...

**Mô tả công việc**: (Mức lương: Thỏa thuận) Mô tả Công việc Group Clinical Trials Unit (CTU) Location This post is based in Ha Noi, with some travel required. Hours of work Full time: Monday - Friday, 37.5 hours per week, extra hours may be required Tenure Initially for 01 year, including a 02-month probation period, with...

JOB ANNOUNCEMENT - CLINICAL RESEARCH COORDINATORPosition: Clinical Research CoordinatorFull-time, based in HanoiReport to: Clinical Research Manager & Investigator of Record (IoR)Position Summary:The Clinical Research Coordinator (CRC) will oversee and perform daily clinical trial activities to ensure the studies are conducted in compliance with protocols,...

**Mô tả công việc**: (Mức lương: Thỏa thuận) Mô tả Công việc Group Clinical Trials Unit Location Base in OUCRU (Hanoi or HCMC) Hours of work Full time: Monday - Friday, 37.5 hours per week, extra hours may be required. Tenure Initially for 01 year, including a 02 month probation period, with possibility of extension. Reporting...

Mô tả công việc:(Mức lương: Thỏa thuận)Mô tả Công việcGroupClinical Trials UnitLocationBase in OUCRU (Hanoi or HCMC)Hours of workFull time: Monday - Friday, 37.5 hours per week, extra hours may be required.TenureInitially for 01 year, including a 02 month probation period, with possibility of extension.Reporting toAWARE1 PIBackgroundThe...

**Job Description**: **THE OPPORTUNITY** - Permanent Headcount with International Pharmaceutical company - Multiple therapeutic area study to explore your clinical experience - Best team and career development with company **WHAT YOU WILL DO** - Develops strong site relationships and ensures continuity of site relationships through all phases of the...

Group Research Location This post is based in Ha Noi, with some travel required. Hours of work 5 hours per week, extra hours may be required. Tenure Initially for 01 year, including a 02 month probation period, with possibility of extension. Reporting to Director of OUCRU Ha Noi Vacancy reference JDHAN_0224_001 Background The Oxford University Clinical...

Job Description:THE OPPORTUNITY Permanent Headcount with International Pharmaceutical company Multiple therapeutic area study to explore your clinical experience Best team and career development with companyWHAT YOU WILL DO Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study...

GroupResearchLocationThis post is based in Ha Noi, with some travel required.Hours of work5 hours per week, extra hours may be required.TenureInitially for 01 year, including a 02 month probation period, with possibility of extension.Reporting toDirector of OUCRU Ha NoiVacancy referenceJDHAN_0224_001BackgroundThe Oxford University Clinical Research Unit...

**Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, Our company policies and procedures, quality standards and adverse event reporting requirements internally and...

**Mô tả công việc**: (Mức lương: Thỏa thuận) Mô tả Công việc Group Research Location This post is based in Ha Noi, with some travel required. Hours of work 37.5 hours per week, extra hours may be required. Tenure Initially for 01 year, including a 02 month probation period, with possibility of extension. Reporting to Director...

Mô tả công việc:(Mức lương: Thỏa thuận)Mô tả Công việcGroupResearchLocationThis post is based in Ha Noi, with some travel required.Hours of work37.5 hours per week, extra hours may be required.TenureInitially for 01 year, including a 02 month probation period, with possibility of extension.Reporting toDirector of OUCRU Ha NoiVacancy...

Job Description:Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...

**Mô tả công việc**: (Mức lương: Thỏa thuận) The post is responsible for the day-to-day operations of the IT activities in the Oxford University Clinical Research Unit - Ha Noi. He/she is also responsible for managing all servers, computers, printers, internet service, networking devices, and backup services by coordinating with IT Teams in...

**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...