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DOSSIÊ MJ-0799 · ACESSO PARCIAL

Senior Clinical Project Manager

Precision Medicine Group · Remote, China

RemotoNão informadoGerente

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Descrição da vaga

<p><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Precision for Medicine is not your typical CRO.&nbsp; 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.&nbsp; 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.</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Position Summary:</span></p> <p><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">The Senior Project Manager plans, directs, coordinates, and delivers activities for designated clinical</span><span style="font-family: arial, helvetica, sans-serif;">-study&nbsp;</span><span style="font-family: arial, helvetica, sans-serif;">projects to ensure that project objectives of quality, scope, cost, and time are accomplished.</span></span></p> <p><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">PM will either manage regional trials (moderate complexity) and/or supportive role in managing complex </span><span style="font-family: arial, helvetica, sans-serif;">global trials. The essential functions below will describe the PM acting in a primary / lead PM role on a </span><span style="font-family: arial, helvetica, sans-serif;">study. When in a supportive role on a global study, the essential functions will be delegated by the Global </span><span style="font-family: arial, helvetica, sans-serif;">Lead.</span></span></p> <p style="text-align: left;"><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Essential functions of the job include but are not limited to:</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Serve as primary point-of-contact and primary escalation point to the client</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Coordinate and oversees all functional services including external vendors to the established </span><span style="font-family: arial, helvetica, sans-serif;">timeline and budget</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Manage the study budget, ensuring project remains within scope and that any out of scope </span><span style="font-family: arial, helvetica, sans-serif;">activities are identified early and handled as appropriate. •&nbsp;Ensure functional areas are fully aware </span><span style="font-family: arial, helvetica, sans-serif;">of the study scope and are managing the scope for their functional areas accordingly.</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Manage the financial health of assigned studies, including oversight of the project profitability, </span><span style="font-family: arial, helvetica, sans-serif;">billable project hours, and compliance with on time, accurate billing and forecasting to support </span><span style="font-family: arial, helvetica, sans-serif;">business objectives.</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Develop robust and comprehensive project plans, including timelines and proactive risk </span><span style="font-family: arial, helvetica, sans-serif;">management and mitigation, to guide all parameters of trial execution with consistency and </span><span style="font-family: arial, helvetica, sans-serif;">quality</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Ensure Quality management for assigned projects, including eTMF Inspection readiness, </span><span style="font-family: arial, helvetica, sans-serif;">implementation of quality notification incident forms and / or corrective and preventative action </span><span style="font-family: arial, helvetica, sans-serif;">plans to address any quality findings.</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Maintain integrated collaboration with all functional operations in the delivery of the program and </span><span style="font-family: arial, helvetica, sans-serif;">review as necessary of other study documentation</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Establish tracking metrics to monitor trial and team progress towards project goals</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Prepare project status updates and report on progress to clients and senior management, </span><span style="font-family: arial, helvetica, sans-serif;">including reporting on key performance indicators, offering solutions and opportunities as they </span><span style="font-family: arial, helvetica, sans-serif;">arise</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Lead both internal and client meetings and set expectations for the project team</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Communicate effectively with client and Precision management to relay protocol/study issues </span><span style="font-family: arial, helvetica, sans-serif;">including any deviations and implements necessary actions in response to those issues</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Ensure study specific training is implemented in collaboration with functional areas and ensure </span><span style="font-family: arial, helvetica, sans-serif;">study specific training compliance for the duration of the project</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Support business development and marketing activities as appropriate, including travel to Bid </span><span style="font-family: arial, helvetica, sans-serif;">Defence meetings as required</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Perform other duties as assigned by management</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Remain compliant with organisational training, time-reporting and any other administrative duties </span><span style="font-family: arial, helvetica, sans-serif;">as required</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Provides on-going feedback for functional team members including annual performance reviews</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Ability to travel domestically and internationally including overnight stays</span></p> <p style="text-align: left;"><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Qualifications:</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Minimum Required:</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Degree or equivalent combination of education/experience in science or health-related </span><span style="font-family: arial, helvetica, sans-serif;">field. Advanced degree preferred</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Minimum of 3-7 years of clinical research experience or proven competencies for this position</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">and a minimum of 2-4 years of leading a project</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Experience managing regional trials (moderate complexity) and/or supportive role in managing</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">complex global trials</span></p> <p style="text-align: left;"><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Other Required:</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project,</span><span style="font-family: arial, helvetica, sans-serif;">eTMF, EDC and CTMS</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Good communication and interpersonal skills to effectively interface with others in a team setting</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Good organizational skills, attention to detail, and a customer service demeanor</span></p> <p style="text-align: left;"><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Competencies:</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as well as the ability to </span><span style="font-family: arial, helvetica, sans-serif;">implement such items</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Working knowledge of project management techniques and tools</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Experience working in a cross-functional project management environment</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Fundamental understanding of cross-functional management</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Fundamental understanding of project planning, risk management and change management with </span><span style="font-family: arial, helvetica, sans-serif;">an awareness of appropriate escalation</span></span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• High level of integrity and must inspire and demand the highest standards from a professional </span><span style="font-family: arial, helvetica, sans-serif;">and ethical perspective</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Ability to lead and inspire excellence within a study team</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Ability to create an environment where study team members have a sense of ownership that will </span><span style="font-family: arial, helvetica, sans-serif;">lead to increases in productivity and efficiency</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Results oriented, accountable, motivated and flexible</span><br><span style="font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">• Good time management, negotiation, critical thinking, decision making, analytical and </span><span style="font-family: arial, helvetica, sans-serif;">interpersonal skills</span></span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Good presentation, verbal and written communications skills</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Fundamental understanding of project management software</span><br><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">• Experience in pharmaceutical and/or device research required</span></p> <p style="text-align: left;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><span style="font-family: arial, helvetica, sans-serif;">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.</span></span></p> <p>&nbsp;</p><div class="content-conclusion"><hr> <p>Any data provided as a part of this application will be stored in accordance with our&nbsp;<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&amp;data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&amp;reserved=0">Privacy Policy.</a>&nbsp;For CA applicants, please also refer to our&nbsp;<a href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&amp;data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&amp;reserved=0">CA Privacy Notice</a>.</p> <p>Precision Medicine Group is 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.</p> <p>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 <a href="mailto:myHR@precisionmedicinegrp.com">myHR@precisionmedicinegrp.com</a>.</p> <p><span data-teams="true"><strong>Recruitment Fraud Warning: </strong>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 <a id="menur2oq" class="fui-Link ___1q1shib f2hkw1w f3rmtva f1ewtqcl fyind8e f1k6fduh f1w7gpdv fk6fouc fjoy568 figsok6 f1s184ao f1mk8lai fnbmjn9 f1o700av f13mvf36 f1cmlufx f9n3di6 f1ids18y f1tx3yz7 f1deo86v f1eh06m1 f1iescvh fhgqx19 f1olyrje f1p93eir f1nev41a f1h8hb77 f1lqvz6u f10aw75t fsle3fq f17ae5zn" href="mailto:myHR@precisionmedicinegrp.com" target="_blank">myHR@precisionmedicinegrp.com</a> so we can investigate and take appropriate action.</span></p> <p><span data-teams="true"><strong><span data-olk-copy-source="MessageBody">Candidates must be legally authorized to work in the country of employment without employer sponsorship.</span></strong></span></p></div>
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