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高级临床项目经理/临床项目经理

雇主

Precision Medicine Group

地点

远程 · 澳大利亚

待遇

A$面议

工作模式

远程

截止日期

12月12日

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岗位摘要

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients.

岗位职责

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.
Position Summary:
The Senior/Project Manager plans, directs, coordinates, and delivers activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.
Essential functions of the job include but are not limited to:
Serve as primary point-of-contact and primary escalation point to the client
Coordinate and oversees all functional services including external vendors to the established timeline and budget
Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate. Independently drive the CO to completion and execution with support as needed.
Maintain integrated collaboration with clinical operations in the delivery and participates in clinical activities as appropriate. For projects of very limited scope (i.e. number of sites), Sr. PM may assume all clinical activities
Manage the financial health of assigned studies, including oversight of the project profitability, billable project hours, and compliance with on time, accurate billing and forecasting to support business objectives.
Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality
Ensure Qualitymanagement for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings.
Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation
Establish tracking metrics to monitor trial and team progress towards project goals
Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise
Leads both internal and client meetings and set expectations for the project team
Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues
Ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients including Bid Defences with proficiency
Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project
Support business development and marketing activities as appropriate, including travel to Bid Defense meetings as required
Perform other duties as assigned by management
Remain compliant with organisational training, time-reporting and any other administrative duties as required
Provides on-going feedback, for functional team members including annual performance reviews
Minimum Required:
Bachelor’s degree or equivalent combination of education/experience in science or health-related
Advanced degree preferred
Minimum of 7 years of clinical research experience or proven competencies for this position and a minimum of 4 years of direct project management experience
Experience in managing complex and global trials
Ability to travel domestically and internationally including overnight stays
Other Required:
Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) Microsoft Project,
eTMF, EDC and CTMS
Proven communication and interpersonal skills to effectively interface with others in a team setting
Proven organizational skills, attention to detail, and a customer service demeanour
Competencies:
Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as well as the ability to
implement such items
Proven knowledge of project management techniques and tools
Direct work experience in a global, cross-functional project management environment
Good understanding of cross-functional management
Good understanding of project planning, risk management and change management with an
awareness of appropriate escalation
Proven experience in strategic planning, risk management and change management
High level of integrity and must inspire and demand the highest standards from a professional
and ethical perspective
Ability to lead and inspire excellence within a study team
Ability to create an environment where study team members have a sense of ownership that will
lead to increases in productivity and efficiency
Results oriented, accountable, motivated and flexible
Proven time management, negotiation, critical thinking, decision making, analytical and
interpersonal skills
Proven presentation, verbal and written communications skills
Good understanding of project management software
In depth proven experience in pharmaceutical and/or device research required
We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Groupis an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at .
Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at so we can investigate and take appropriate action.
Originally posted on Himalayas

申请条件

- 具备项目管理经验,能够规划、指导、协调和交付指定临床研究项目
- 能够作为客户的主要联系人和主要升级点
- 具备协调和监督所有职能服务(包括外部供应商)的能力,确保符合时间线和预算
- 能够管理研究预算,确保项目在范围内,并识别和处理范围外活动
- 能够独立推动变更订单(CO)的完成和执行
- 具备与临床运营团队协作的能力,并适当参与临床活动
- 对于范围非常有限的项目(如站点数量少),能够承担所有临床活动
- 能够管理指定研究的财务健康,包括监督项目盈利能力、可计费项目小时数,以及合规的按时、准确计费和预测
- 能够制定稳健且全面的项目计划,包括时间线和主动风险管理与缓解
- 能够确保指定项目的质量管理,包括eTMF检查准备、质量通知事件表单的实施和/或纠正与预防措施
- 优先考虑具有肿瘤学和罕见病领域经验
- 优先考虑具有生命科学、临床研究或相关领域的学士或更高学位
- 优先考虑具有CRO(合同研究组织)或相关行业经验
- 具备出色的沟通、领导和问题解决能力

雇主简介

Precision Medicine Group 是一家专注于精准医疗领域的公司,提供相关专业服务。

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数据来源:Himalayas

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