位于北京市的 18 个优质project associate职位（正在招聘！）

Senior Clinical Research Associate
Agilent Technologies (China) Co., Ltd. —北京市
Cross Technology Managed Services Engineer (L2)
NTT Ltd —北京市
- 全职
SM/AD, MCICC - Evaluation
MSD —北京市
- 全职
Senior Data Scientist
London Stock Exchange Group —北京市
- 全职
Clinical Specialist
Medtronic —北京市
- 全职
FSP Clin Ops Delivery Associate III
Thermo Fisher Scientific —北京市
- 全职
2天
Business Development Manager - International Real Estate Developer - Beijing
KITE Search —北京市
- 全职
快速申请
Procurement Manager
Brii Biosciences —北京市
- 全职
Cross Technology Managed Services Engineer (L2)
NTT DATA —北京市
- 全职
Principal QA Engineer
London Stock Exchange Group —北京市
- 全职
2天
Director, GSO & ASO, Beijing
Marriott International, Inc —北京市
- 全职
Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)
IQVIA —北京市
- 全职
CTM I - Shanghai
サイネオス・ヘルス —北京市
CRA II - Beijing
Syneos - Clinical and Corporate - Prod —北京市
- 全职
Computer Engineer
GE HEALTHCARE —北京市
Senior/Clinical Research Associate
Precision Medicine Group —北京市
CRAI
サイネオス・ヘルス —北京市
3天
FSP Sr CRA (Level I)
Thermo Fisher Scientific —北京市
- 全职
1天

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Senior Clinical Research Associate

Agilent Technologies (China) Co., Ltd.
北京市

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职位详情

完整职位描述

Job Description

Responsible for scheduling and conduct of pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan.
Ensures the HGRAC and IRB submission and approval.
Ensures assigned sites are conducting studies according to protocol requirements and applicable regulations and guidelines.
Ensure that the rights and wellbeing of human subjects are protected.
Ensure the trial data are accurate, complete, and verifiable from source documents.
Verifies that the investigator is enrolling only eligible subjects.
Performs verification of source documents against Case Report Form/Electronic Data Capture entries to assure accurate and complete data.
Ensures that any corrections are appropriately documented by authorized site staff.
Performs Investigational Product accountability, including product storage, inventory, return/destruction, and dispensing/receipt records.
Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
Communicates deviations from the protocol, SOPs, and/or GCP, to the investigator, and project management team and takes appropriate action to prevent recurrence.
Delivers quality written reports, confirmation and follow-up letters within timelines of SOPs and Monitoring Plans.
Ensure that the trial is conducted and documented properly from study start-up through close-out.
Participates in site audits, as requested.
May conduct site and study feasibility assessments.
May be involved in the development of monitoring guideline and tools.
Support study monitoring from other BU as needed.

Qualifications

Bachelors or Masters Degree or University Degree or equivalent.
At least 3 years CRA working experience in multinational pharmaceutical, Medical Device company or CRO.
Have Medical Device or IVD clinical trials experience.
Familiar with clinical trial Quality Management System.
Good English skills, willing to learn, hard working.
Candidate should be major in clinical medicine or pharmacy; Pathology would be a plus.
10% domestic travel.

Additional Details

This job has a full time weekly schedule.

Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required:

10% of the Time

Shift:

Day

Duration:

No End Date

Job Function:

Medical/Clinical

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在北京市的project associate个职位

Senior Clinical Research Associate

Cross Technology Managed Services Engineer (L2)

SM/AD, MCICC - Evaluation

Senior Data Scientist

Clinical Specialist

FSP Clin Ops Delivery Associate III

Business Development Manager - International Real Estate Developer - Beijing

Procurement Manager

Cross Technology Managed Services Engineer (L2)

Principal QA Engineer

Director, GSO & ASO, Beijing

Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)

CTM I - Shanghai

CRA II - Beijing

Computer Engineer

Senior/Clinical Research Associate

CRAI

FSP Sr CRA (Level I)

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