10 个优质trial associate职位（正在招聘！）

Study Manager (Insourced to MNC), Shanghai
Caidya —上海市
Process Engineer (Tooling Expert)_PS_RBCD
Bosch Group —无锡市
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(Senior) Clinical Research Associate (CRA)
IQVIA —广州市
MSL Lead -BC East
Novartis —上海市
- 全职
5天
PG Sales Engineer
Air Prod&Chem (Shanghai) —无锡市
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Clinical Trials Assistant (Guangzhou)
IQVIA —广州市
7天
Clinical Research Associate II
ICON Plc —武汉市
- 全职
1天
CRA I - Guangzhou
サイネオス・ヘルス —广州市
2天
Study Manager (Insourced to MNC)
Caidya —中国
CRA II - Beijing
サイネオス・ヘルス —中国
7天

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Process Engineer (Tooling Expert)_PS_RBCD
Bosch Group —无锡市
Ensure all tooling activities comply with Bosch quality and safety standards. Continuous Improvement: Identify and implement improvements to die design, tooling…
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Study Manager (Insourced to MNC), Shanghai

Caidya -
上海市

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职位详情

完整职位描述

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Job Description:
1. Study management

Accountable for conducting country and study level feasibility, review Pre-Trial Assessment (PTA) output to ensure appropriate site selection in China.
Provide comprehensive operational input to the protocol design to ensure operational feasibility.
Accountable for the development of realistic detailed study startup and monitoring plans.
Develop study level recruitment/retention strategy/plan; oversee implementation of plan, including site-level plans, recruitment/retention tools, and advertising materials.
Assess and oversee site activation plans to ensure timely site readiness (Clinical Site Agreements, Ethics Committee approvals and regulatory documentation.)
Provides ongoing assessment of subject enrollment / discontinuations to inform accurate forecasting for financial planning.
Generate study/country level ICD and review site level ICD as appropriate.
Accountable for the delivery of the study against approved plans.
Coordinates study/protocol training& investigator meeting.
The Study Manager will be the technical expert for study management systems and processes.
The Study Manager will champion the implementation and use of harmonized, consistent processes and excellence in Study Management deliverables related to cost-effective, timely, and high-quality clinical trial data according to agreed global goals.
Accountable for HGRAC submission package preparation by working with HGRAC taskforce team
Help to address Significant Quality Events or other quality issues at patient/site level.

2. Site monitoring and oversight

Monitor site performance using appropriate tools and resources (e.g., study metrics, site health, Risk based monitoring etc.) and take appropriate mitigate actions.• Lead risk assessment at the site/country level for their studies, including identifications of mitigation and control.
Conduct and report oversight activities, both remote and onsite visits, according to Pfizer requirements and standards.
Perform additional oversight visits/reviews based on the type of issues that arise during the course of a study, and the analytics and visualizations outputs.

3. Budget

Develops and provides key inputs to Clinical Trial Budget (CTB) (e.g., Per Subject Costs- PSCs).
Responsible for study budget phasing and tracking.
Develop study and country level CSA template and review and approve Site CSA/contracts.
Review and approve payments to investigators and vendors.

4. Drug Supply

Collaborate with Supply Chain Lead to develop and complete the Request for Clinical Supplies.
Work with the Supply Chain Lead to ensure that clinical trial drug supplies are ordered, produced,

labeled and supplied in a timely manner.

Approves & oversees drug supply management – manages flow of drug supply to the sites & set up Integrated Voice Response System (IVRS) with Supply Chain Lead.

5. Inspection/audit Readiness

For study-specific audits and inspections, the study manager can serve as a resource to the study team to facilitate the facilitate the audit/inspection.
Leads inspection readiness activities related to study management and site readiness.
May support study level submission readiness"

Qualifications:

Minimum of BS/BA in a biomedical discipline or equivalent education/training is required
At least 5 years in clinical practices
Good working knowledge of Good Clinical Practices (GCPs), monitoring, clinical drug development process and country regulatory environment
Experience with clinical research methodology (e.g., study design, study monitoring and data analysis). Prior study management and/or study coordination experience preferred.
Demonstrated effectiveness in working in a multidisciplinary, matrix team situation.
Advanced education and/or training/experience desirable.

Skills:

Extensive knowledge of clinical development process including in depth knowledge and understanding of the principles of GCP.
Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies.
Knowledge of global and local regulatory requirement, disease and technical areas pertaining to clinical studies.
Ability to manage studies and processes to agreed quality and timelines.
Ability to proactively identify & mitigate risks around study/site level in study execution.
Keen problem-solving skills.
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.

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trial associate 个职位

Study Manager (Insourced to MNC), Shanghai

Process Engineer (Tooling Expert)_PS_RBCD

(Senior) Clinical Research Associate (CRA)

MSL Lead -BC East

PG Sales Engineer

Clinical Trials Assistant (Guangzhou)

Clinical Research Associate II

CRA I - Guangzhou

Study Manager (Insourced to MNC)

CRA II - Beijing

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我想收到 trial associate 的最新职位提醒

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