# Clinical Project Manager II Remote from[USA](https://jobicy.com/job-region/usa.md)Annual salary Undisclosed Salary information is not provided for this position. Check our [Salary Directory](https://jobicy.com/salaries.md) to estimate the average compensation for similar roles.Department [Project Management](https://jobicy.com/categories/project-management.md) Employment type Full Time, Job posted20 Jul 2026Apply before20 Aug 2026Experience level Midweight Views / Applies 176 / 13 [About company](https://jobicy.com/company/clinchoice.md) * Share About [ClinChoice](https://jobicy.com/company/clinchoice.md) Medical innovation with over 25 years of trust and experience. [Pharmaceuticals](https://jobicy.com/company-category/pharmaceuticals.md) * 1997 Verified job posting This job post has been [manually reviewed](https://jobicy.com/tools/help-center/employee/how-does-jobicy-verify-the-legitimacy-of-remote-job-listings.md) for authenticity and compliance. ### AI Summary ClinChoice is hiring a Clinical Project Manager II to oversee oncology and hematology clinical trials for a global CRO. The role involves managing study execution, vendor and site activities, budgets, and compliance with GCP/ICH guidelines. Candidates need prior CRO experience and strong project management skills. This is a remote position based in Horsham, Pennsylvania, offering the opportunity to work with a diverse client portfolio. The company emphasizes a quality-driven culture and professional growth. ### Role DNA Job Complexity Easy Hard Pace & Pressure Relaxed Fast-paced Autonomy Level Guided Full Ownership Communication Load Independent Highly Collaborative AI Insight Managing complex oncology hematology trials with budget responsibility, multiple vendors, and strict regulatory compliance requires advanced skills and experience, hence difficulty level 4. ### Salary Analysis Median Highly Competitive $110,000US Market $90k – 130k 0 $143k AI Insight The offered salary is not specified, but for a Clinical Project Manager II with CRO experience and oncology focus, the market range is $90,000-$130,000, which is competitive for this role based on US market data. ### Core Skills Required [Clinical Project Management](https://jobicy.com/jobs?search_keywords=Clinical+Project+Management.md) [Oncology](https://jobicy.com/jobs?search_keywords=Oncology.md) [Hematology](https://jobicy.com/jobs?search_keywords=Hematology.md) [CRO](https://jobicy.com/jobs?search_keywords=CRO.md) [GCP](https://jobicy.com/jobs?search_keywords=GCP.md) [ICH Guidelines](https://jobicy.com/jobs?search_keywords=ICH+Guidelines.md) [Budget Management](https://jobicy.com/jobs?search_keywords=Budget+Management.md) [Vendor Management](https://jobicy.com/jobs?search_keywords=Vendor+Management.md) [Clinical Trials](https://jobicy.com/jobs?search_keywords=Clinical+Trials.md) [Regulatory Compliance](https://jobicy.com/jobs?search_keywords=Regulatory+Compliance.md) ### Cover Letter Sample Dear Hiring Manager, I am writing to express my interest in the Clinical Project Manager II position at ClinChoice. With over six years of experience in clinical research and a strong background in managing complex oncology and hematology trials, I am confident in my ability to deliver high-quality results and contribute to your team. In my current role at a CRO, I have successfully led cross-functional teams, managed budgets, and ensured compliance with GCP/ICH guidelines. My experience includes overseeing vendor relationships, monitoring site activities, and implementing corrective actions to keep projects on track. I am particularly drawn to ClinChoice's quality-driven culture and global reach. I am eager to bring my project management expertise and passion for advancing treatments to your organization. Thank you for considering my application. I look forward to the opportunity to discuss how my skills align with your needs. Sincerely, [Your Name] Copy ### Sample Interview Questions Describe your experience managing complex oncology clinical trials. What challenges did you face and how did you overcome them?In my previous role, I managed a phase III oncology trial with multiple sites globally. Challenges included patient recruitment delays and data discrepancies. I implemented a risk-based monitoring plan and enhanced site communication, which improved recruitment by 20% and data quality.How do you ensure project milestones are met within budget and timelines?I use project management tools like MS Project and CTMS to track progress, conduct regular budget reviews, and identify potential risks early. I also hold weekly team meetings to address issues and adjust resources as needed.Can you give an example of how you handled a vendor performance issue?Once, a lab vendor had turnaround time delays. I scheduled a meeting to discuss expectations, implemented a performance improvement plan with weekly status updates, and liaised with procurement. The vendor improved turnaround time by 30% within a month.How do you stay updated on GCP/ICH guidelines and regulatory changes?I subscribe to regulatory updates from FDA and EMA, attend industry webinars, and participate in internal training sessions. I also encourage my team to share relevant changes during team meetings.Describe a time you had to manage a difficult stakeholder. How did you handle it?A client had unrealistic expectations regarding timeline. I scheduled a meeting to present data on typical timelines and proposed a revised schedule with clear milestones. By maintaining transparency and offering solutions, we reached an agreement that satisfied both parties. ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Clinical Project Manager II to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes. In this role, you will be responsible for the execution, oversight and delivery of clinical studies, including study tracking and management of vendor, site, and CRO activities. Candidates should have prior CRO experience and a strong background managing complex oncology and hematology clinical trials. This is a permanent remote opportunity with potential hybrid arrangement depending on location; our office is based in Horsham, Pennsylvania. Only candidates with previous CRO experience will be considered. Join our global team and help create a healthier world! Main Job Tasks and Responsibilities: * Organizes and participates in Monitor’s and Investigator’s Meetings. * Performs, if necessary, co-monitoring visits for the assigned clinical projects. * Carries out, after appropriate and documented training/past experiences, the monitoring of the sites for the assigned projects, when requested and if applicable. * May act as Feasibility Associate (FEA) after appropriate and documented training. * Review and approve third party invoices for payment. Review and approve contractor timesheets for alliance with agreed scope of work. * Develop and implement alternative solutions to problems with study timelines, resources, budgets, etc. * Ensure issues are identified and communicated by the study team. Implement corrective action plan to prevent repetition of critical issues. * Assess scope of work and timelines against contractual agreements and identify change orders pro-actively. * Manage any deviations on resources and hours spent on the project to be able to evaluate the project progress and profitability and identify change orders in a timely manner and implement corrective actions. Ensure budget discrepancies are documented. * Submit invoice requests, trial related invoices and payment authorizations to finance in a timely manner. * Regularly track all expenditure and review for consistency with trial budgets. * Organize quality check of filing of key study documentation. * Ensure all administrative close-out procedures are completed. * Follow and comply with the Company’s QMS, ISMS and PIMS requirements. Education, Experience and Skills: * University Degree in scientific, medical or paramedical disciplines. * Three (3) years (at least) of Project Management experience in the CRO/Pharmaceutical industry or six (6) years (at least) of experience as CM/CRA in a CRO/Pharmaceutical industry. * Excellent knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements. * Experience managing complex clinical studies-oncology and hematology required. * Excellent English communication skills:written and verbal. * Proficient in the use of computer software systems (Word, Excel, PowerPoint, Microsoft Project, Share Point, CTMS, timesheet software, EDC software, etc.). * Ability to travel as required. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare! Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Project Manager, Clinical Project Manager, Senior Study Manager, Senior Clinical Trial Manager, Study Management, Project Management, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Study Management, Project Leader, Project Lead, complex clinical trials, oncology, hematology, respiratory, CRO, Contract Research Organization, clinical trials, phase I-IV studies #LI-VH1 #LI-PM II #LI-FULLTIME Show more [Apply now >](https://jobicy.com/jobs/149469-clinical-project-manager-ii.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. 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