[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) # Clinical Trial 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[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceSeniorPublished18 Oct 2026Apply before17 Nov 2026Listing views31Application 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. This Clinical Trial Manager leads the operational planning, execution, and oversight of clinical studies, with a particular focus on oncology and rare-disease programs. The role is the primary clinical contact for clients and coordinates CRAs, CTAs, sites, vendors, regulatory teams, data management, quality assurance, and project management. Key responsibilities include feasibility and recruitment planning, site startup and oversight, monitoring strategy, eTMF management, metric reporting, audit readiness, CAPA implementation, and investigational-product accountability. Candidates need a science or health-related background, substantial clinical monitoring experience, and at least 5–8 years of clinical research experience. The position is remote in China and requires experience supporting the China market. ## 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 insightThis is a senior, highly regulated trial-operations role requiring broad ownership of study delivery, quality, timelines, vendors, sites, and cross-functional risks. Success depends on deep ICH-GCP knowledge, strong clinical operations judgment, and the ability to manage complex stakeholder and compliance issues independently. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$85,000US market range (per year)$65k–$110k0$121.00k 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 yearly cadence and USD 85,000 median estimate are inferred for a full-time Clinical Trial Manager supporting the China market; the estimated annual market range is USD 65,000–110,000 and is not employer-verified. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial management](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20management.md)[ICH-GCP compliance](https://jobicy.com/jobs?search_keywords=ICH-GCP%20compliance.md)[Clinical operations](https://jobicy.com/jobs?search_keywords=Clinical%20operations.md)[Clinical monitoring](https://jobicy.com/jobs?search_keywords=Clinical%20monitoring.md)[Oncology trials](https://jobicy.com/jobs?search_keywords=Oncology%20trials.md)[Rare disease research](https://jobicy.com/jobs?search_keywords=Rare%20disease%20research.md)[Site feasibility](https://jobicy.com/jobs?search_keywords=Site%20feasibility.md)[Patient recruitment](https://jobicy.com/jobs?search_keywords=Patient%20recruitment.md)[eTMF management](https://jobicy.com/jobs?search_keywords=eTMF%20management.md)[CAPA management](https://jobicy.com/jobs?search_keywords=CAPA%20management.md)[Regulatory submissions](https://jobicy.com/jobs?search_keywords=Regulatory%20submissions.md)[Vendor management](https://jobicy.com/jobs?search_keywords=Vendor%20management.md)[Clinical data review](https://jobicy.com/jobs?search_keywords=Clinical%20data%20review.md)[CTMS reporting](https://jobicy.com/jobs?search_keywords=CTMS%20reporting.md)[Investigational product accountability](https://jobicy.com/jobs?search_keywords=Investigational%20product%20accountability.md) Sample interview questionsHow do you build and maintain a study plan that protects timelines and quality?I translate the protocol and scope of work into a detailed operational plan with clear owners, milestones, dependencies, risks, and escalation paths. I review performance metrics regularly with the study team and adjust monitoring, resourcing, or site-support activities early when indicators show a risk to enrollment, data quality, or timelines. Describe your approach to feasibility and recruitment planning for a clinical study in China. I begin with protocol complexity, the target patient population, competitive-study activity, and realistic site capabilities. I work closely with local investigators and stakeholders to validate assumptions, select suitable sites, establish country-specific recruitment and retention actions, and monitor enrollment trends against contracted commitments. How would you respond if a site repeatedly has protocol deviations or poor data quality? I would first confirm the root cause through a review of monitoring findings, source documentation, training history, and operational constraints. I would then implement a documented corrective and preventive action plan with targeted retraining, clear deadlines, and increased oversight where needed, while escalating material compliance risks to the appropriate internal and sponsor stakeholders. What steps do you take to ensure audit readiness throughout a trial? I treat audit readiness as a continuous process rather than a late-stage activity. This includes maintaining a complete and current eTMF, tracking essential documents and approvals, ensuring monitoring documentation is timely, reviewing compliance metrics, and promptly resolving findings through well-documented CAPAs. How do you manage communication across CRAs, vendors, investigators, project management, and the client? I establish a regular governance cadence with concise status reporting, action logs, decision records, and defined escalation routes. I tailor communications to the audience while ensuring that risks, responsibilities, and deadlines are transparent, and I follow up consistently until critical actions are closed. 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. We are hiring for a Clinical Trial Manager. Position Summary: Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements. Essential functions of the job include but are not limited to: * Primary clinical point of contact with the client * Collaborate with PM on monthly invoicing and variance management of clinical budget * Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials) * Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings * Generate potential site list from key stakeholders and drive site feasibility process * Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment * Develop and finalize the country recruitment/retention strategy * Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures * Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs * Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate * Support in planning and conducting investigator meetings * Review and/or approve of IP release packages * Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable * Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables * Generate and utilize metric reporting (e.g. CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate * Responsible for eTMF implementation and management * Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure * Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits * Work closely with PM for project-specific resourcing issues * Escalate pertinent CRA performance and site compliance issues when necessary * Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines * Manage processes for investigational product (IP) including drug accountability and reconciliation * When a cross-functional PM is not assigned to a given program, the CTM will assume project management responsibility as needed * Supports business development and marketing activities as appropriate * May negotiate site budget and investigator contract with support from the legal department and/or site contracts group * May review site visit reports and ensures monitoring (i.e. scheduling and scope) is executed per monitoring plan * May be responsible for management of clinical vendors (e.g. labs, IP, patient diary, home health care) in conjunction with PM * May perform clinical data review of patient profiles, data listings and summary tables, including query generation * May have line management responsibilities * May manages workload of supervised staff with continued assessment and adjustment as needed * Perform other duties as assigned by management Qualifications: Minimum Required : * Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred * Minimum of 5-8 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience. Oncology trial experience preferred. * Regional experience required to cover China market 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/155670-clinical-trial-manager-2.md) > Annual salary information is not provided for this position. Explore salary ranges for similar roles in our [Salary Directory ›](https://jobicy.com/salaries.md) * ![Upload CV](data:image/svg+xml;base64,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) ### Upload your resume now To unlock remote work opportunities and be discovered by global employers. This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content. Next step ## Apply now. Follow the employer’s application method and review Jobicy’s safety guidance before sharing personal information. Keep exploring ## Related remote jobs. * ![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg) Precision Medicine Group Oct 18 New ### [Feasibility Manager](https://jobicy.com/jobs/155686-feasibility-manager.md) Due to our continued growth, Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK,… * ![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg) Precision Medicine Group Oct 18 New ### [Clinical Research Associate II](https://jobicy.com/jobs/155683-clinical-research-associate-ii.md) 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,… * ![Precision Medicine Group logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/f1277044-221.jpg) Precision Medicine Group Oct 18 New ### [Clinical Research Associate I/ Clinical Research Associate II](https://jobicy.com/jobs/155681-clinical-research-associate-i-clinical-research-associate-ii.md) 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,… * ![Montu UK logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/ebb2a836-221.png) Montu UK Oct 18 New ### [Consultant Psychiatrist PAYE](https://jobicy.com/jobs/155650-consultant-psychiatrist-paye.md) An opportunity to help patients who have run out of options For many people living with chronic pain, the journey has been long. They have tried multiple medications, procedures and… * ![Montu UK logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/ebb2a836-221.png) Montu UK Oct 17 New ### [Consultant Pain Management PAYE](https://jobicy.com/jobs/155615-consultant-pain-management-paye.md) An opportunity to help patients who have run out of options For many people living with chronic pain, the journey has been long. They have tried multiple medications, procedures and… * ![Montu UK logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/ebb2a836-221.png) Montu UK Oct 17 New ### [Pain Consultant (Remote, Ireland)](https://jobicy.com/jobs/155612-pain-consultant-remote-ireland.md) An opportunity to help patients who have run out of options. For many people living with chronic pain, the journey has been long. They have tried multiple medications, procedures and… * ![Montu UK logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/ebb2a836-221.png) Montu UK Oct 17 New ### [Women’s Health Consultant (Remote, Ireland)](https://jobicy.com/jobs/155609-womens-health-consultant-remote-ireland.md) Too many women spend years being told their pain is normal. They wait a long time for a diagnosis, cycle through treatments that do not work for them, and often… * ![Baylor College of Medicine logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/09/189b5633-221.png) Baylor College of Medicine Oct 17 New ### [Senior Clinical Applications Associate – Cadence/Hello World/MyChart](https://jobicy.com/jobs/150669-senior-clinical-applications-associate-cadence-hello-world-mychart.md) Summary The Senior Clinical Applications Associate provides technical and operational support for Epic applications supporting patient engagement, access, and digital front door capabilities at Baylor College of Medicine. This role… * ![Alimentiv logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/d11f5845-221.png) Alimentiv Oct 17 New ### [Clinical Operations Lead (Clinical Trial Manager)](https://jobicy.com/jobs/150857-clinical-operations-lead-clinical-trial-manager.md) Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the… * ![Dandy logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/2321b7db-221-1.jpeg) Dandy Oct 16 New ### [Dental Field Trainer – California Bay Area](https://jobicy.com/jobs/155524-dental-field-trainer-california-bay-area.md) Dandy is transforming the massive and antiquated dental industry—an industry worth over $400B. Backed by some of the world’s leading venture capital firms, we’re on an ambitious mission to simplify… [Browse all jobs](https://jobicy.com/jobs.md)