[All remote jobs](https://jobicy.com/jobs.md)[![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg)](https://jobicy.com/company/precision-medicine-group.md)[Precision Medicine Group](https://jobicy.com/company/precision-medicine-group.md) # Senior Clinical Project Manager Review the role, location requirements, compensation details, and application process before deciding whether this opportunity fits your next career move. [Apply for this job](#job-application)[View company](https://jobicy.com/company/precision-medicine-group.md)ShareRemote from[China](https://jobicy.com/job-region/china.md)SalaryUndisclosedDepartment[Project & Program Management](https://jobicy.com/categories/project-management.md)EmploymentFull TimeExperienceSeniorPublished26 Oct 2026Apply before25 Nov 2026Listing views47Application actions1Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. AI Summary ## The role, at a glance. Senior Clinical Project Manager will lead regional clinical trials of moderate complexity and support complex global studies for a specialist CRO focused on oncology and rare disease. The role owns client communication, cross-functional delivery, vendors, study budgets, timelines, risks, quality activities, and project reporting. It requires clinical research experience, prior project leadership, and working knowledge of ICH-GCP, eTMF, EDC, CTMS, and clinical-trial operations. The position involves international travel, leadership of internal and client meetings, and close oversight of study financial health and compliance. This is a full-time remote role based in China. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 5/5EasyHard ### Pace & Pressure 5/5RelaxedFast-paced ### Autonomy Level 5/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThe role carries end-to-end accountability for clinical-study delivery, client escalations, budgets, quality readiness, and cross-functional coordination. It requires sound judgment in regulated clinical research while managing competing timelines, risks, and stakeholder expectations. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$55,000US market range (per year)$40k–$75k0$82.50k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. No employer compensation was disclosed. The annual cadence is inferred from the regular full-time senior project-management role; the displayed USD range is an AI estimate for comparable clinical project-management work in China and is not verified employer pay. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial management](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20management.md)[Project planning](https://jobicy.com/jobs?search_keywords=Project%20planning.md)[ICH-GCP](https://jobicy.com/jobs?search_keywords=ICH-GCP.md)[Budget management](https://jobicy.com/jobs?search_keywords=Budget%20management.md)[Risk management](https://jobicy.com/jobs?search_keywords=Risk%20management.md)[Vendor management](https://jobicy.com/jobs?search_keywords=Vendor%20management.md)[Client relationship management](https://jobicy.com/jobs?search_keywords=Client%20relationship%20management.md)[eTMF](https://jobicy.com/jobs?search_keywords=eTMF.md)[Electronic data capture](https://jobicy.com/jobs?search_keywords=Electronic%20data%20capture.md)[Clinical trial management systems](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20management%20systems.md)[Quality management](https://jobicy.com/jobs?search_keywords=Quality%20management.md)[CAPA](https://jobicy.com/jobs?search_keywords=CAPA.md)[Cross-functional leadership](https://jobicy.com/jobs?search_keywords=Cross-functional%20leadership.md)[Microsoft Project](https://jobicy.com/jobs?search_keywords=Microsoft%20Project.md)[Clinical research](https://jobicy.com/jobs?search_keywords=Clinical%20research.md) Sample interview questionsHow do you develop and maintain a clinical study plan when timelines, vendors, and internal functions have interdependencies?I begin by defining the scope, milestones, critical path, decision owners, and functional deliverables. I build an integrated plan with dependencies and risk triggers, review it regularly with each workstream, and use clear escalation paths when a change could affect quality, cost, or timelines. Describe how you would address a significant risk to enrolment or a study milestone. I would quantify the impact, identify root causes with the relevant functional leads, and document mitigation options with owners and deadlines. I would communicate the risk and recommended path to the client early, then track the selected actions through resolution and update the forecast accordingly. What is your approach to ensuring eTMF inspection readiness throughout a study? I establish document ownership, expected filing timelines, review cadence, and quality metrics at study start. I monitor completeness and timeliness throughout execution, investigate gaps promptly, and coordinate corrective and preventive actions when quality findings occur. How do you manage a client request that falls outside the agreed study scope? I clarify the request, assess operational, budgetary, and timeline impacts with the functional team, and document the change. I present transparent options to the client and ensure appropriate approval and change-control steps are completed before work proceeds. How do you lead a cross-functional team when priorities conflict? I align the team around patient safety, data quality, protocol requirements, and the agreed study objectives. I make dependencies and trade-offs visible, facilitate fact-based decisions, assign accountable owners, and escalate promptly when a decision requires sponsor or senior-management input. Opportunity details ## About this role. 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. PM will either manage regional trials (moderate complexity) and/or supportive role in managing complex global trials. The essential functions below will describe the PM acting in a primary / lead PM role on a study. When in a supportive role on a global study, the essential functions will be delegated by the Global Lead. 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. • Ensure functional areas are fully aware of the study scope and are managing the scope for their functional areas accordingly. • 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 Quality management 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 • Lead 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 • 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 Defence 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 • Ability to travel domestically and internationally including overnight stays Qualifications: Minimum Required: • Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • Minimum of 3-7 years of clinical research experience or proven competencies for this position and a minimum of 2-4 years of leading a project • Experience managing regional trials (moderate complexity) and/or supportive role in managing complex global trials Other Required: • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project,eTMF, EDC and CTMS • Good communication and interpersonal skills to effectively interface with others in a team setting • Good organizational skills, attention to detail, and a customer service demeanor Competencies: • Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as well as the ability to implement such items • Working knowledge of project management techniques and tools • Experience working in a cross-functional project management environment • Fundamental understanding of cross-functional management • Fundamental understanding of project planning, risk management and change management with an awareness of appropriate escalation • 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 • Good time management, negotiation, critical thinking, decision making, analytical and interpersonal skills • Good presentation, verbal and written communications skills • Fundamental understanding of project management software • 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.](https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&reserved=0) For CA applicants, please also refer to our [CA Privacy Notice](https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&reserved=0). 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. 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 [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com). 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 [myHR@precisionmedicinegrp.com](mailto:myHR@precisionmedicinegrp.com) so we can investigate and take appropriate action. Candidates must be legally authorized to work in the country of employment without employer sponsorship. Show more [Apply now >](https://jobicy.com/jobs/157158-senior-clinical-project-manager.md) > Annual salary information is not provided for this position. 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