# Clinical Trial Manager (LATAM) Remote from[Brazil](https://jobicy.com/job-region/brazil.md), [Mexico](https://jobicy.com/job-region/mexico.md) +1 more, [Argentina](https://jobicy.com/job-region/argentina.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 posted3 Jul 2026Apply before3 Aug 2026Experience level Senior Views / Applies 28 / 2 [About company](https://jobicy.com/company/precision-medicine-group.md) * Share About [Precision Medicine Group](https://jobicy.com/company/precision-medicine-group.md) We collaborate from home offices and high-tech facilities to help life science companies move discoveries from molecule to medicine cabinets. [Biotechnology](https://jobicy.com/company-category/biotechnology.md) * 2012 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 This is a senior Clinical Trial Manager role based in Mexico, responsible for leading clinical operations across Latin America. The position involves planning, executing, and overseeing clinical studies, acting as the primary client contact, and ensuring compliance with protocols and regulations. The role offers significant career growth opportunities as the regional team expands. The ideal candidate will have extensive experience in clinical trial management, GCP, and regulatory requirements. ### Role DNA Job Complexity Easy Hard Pace & Pressure Relaxed Fast-paced Autonomy Level Guided Full Ownership Communication Load Independent Highly Collaborative AI Insight The role involves managing complex clinical trials across multiple countries in Latin America, requiring deep knowledge of regulatory environments, GCP, and strong leadership to coordinate with clients, sites, and teams. ### Salary Analysis Median Market Rate $120,000US Market $90k – 160k 0 $176k AI Insight No salary was provided in the listing. Based on US market data for Clinical Trial Managers, the estimated median salary is $120,000 per year. The range typically spans $90,000 to $160,000, depending on experience and location. For a role covering LATAM, compensation may also include benefits and potential adjustments for cost of living. ### Core Skills Required [Clinical Trial Management](https://jobicy.com/jobs?search_keywords=Clinical+Trial+Management.md) [GCP](https://jobicy.com/jobs?search_keywords=GCP.md) [Regulatory Affairs](https://jobicy.com/jobs?search_keywords=Regulatory+Affairs.md) [LATAM](https://jobicy.com/jobs?search_keywords=LATAM.md) [Site Management](https://jobicy.com/jobs?search_keywords=Site+Management.md) [CRO Management](https://jobicy.com/jobs?search_keywords=CRO+Management.md) [Project Management](https://jobicy.com/jobs?search_keywords=Project+Management.md) [Data Management](https://jobicy.com/jobs?search_keywords=Data+Management.md) [Team Leadership](https://jobicy.com/jobs?search_keywords=Team+Leadership.md) [Budget Management](https://jobicy.com/jobs?search_keywords=Budget+Management.md) ### Cover Letter Sample Dear Hiring Manager, I am writing to express my strong interest in the Clinical Trial Manager (LATAM) position. With over 8 years of experience in clinical operations across multiple countries in Latin America, I have successfully led cross-functional teams and managed complex trials in compliance with ICH-GCP and local regulations. My background includes driving site startup, enrollment strategies, and quality oversight. I am particularly drawn to this role because of the opportunity to build and scale a regional team. I have a proven track record of mentoring CRAs and fostering partnerships that ensure timely and high-quality deliverables. I am confident that my skills in strategic planning and client management will contribute to your rapid growth in the region. Thank you for considering my application. I look forward to the possibility of discussing how I can help advance your clinical programs in Latin America. Sincerely, [Your Name] Copy ### Sample Interview Questions Describe your experience managing clinical trials in Latin America. What were the key challenges and how did you overcome them?I have managed trials in Mexico, Brazil, and Argentina. Key challenges included regulatory diversity and language barriers. I overcame them by building local expertise, establishing strong relationships with authorities, and standardizing processes across countries.How do you ensure compliance with ICH-GCP and local regulations across multiple sites?I implement robust monitoring plans, conduct regular training for site staff, and use centralized risk-based monitoring tools. I also maintain close communication with regulatory consultants in each country to stay updated on changes.Can you provide an example of how you managed a difficult client or stakeholder?Once, a client was dissatisfied with enrollment rates. I organized a joint meeting to review feasibility data and co-developed a revised recruitment strategy incorporating site feedback. This improved enrollment by 30% and strengthened our relationship.How do you prioritize tasks when managing multiple clinical studies simultaneously?I use project management software to track milestones and risk. I delegate tasks to capable team members and hold weekly status meetings. I also set clear priorities with clients and adjust resources as needed.What strategies do you use to identify and mitigate risks in clinical trials?I conduct thorough feasibility assessments, use predictive analytics for enrollment, and establish contingency plans for site activation delays. I also encourage a culture of open communication to identify issues early. We’re hiring a Clinical Trial Manager to help build and lead our expanding clinical operations across Latin America. This is an exciting, high‑impact opportunity based in Mexico, supporting rapid growth across Mexico, Brazil, Argentina, Colombia, Chile, and Peru. As the clinical lead, you’ll own the planning, execution, and oversight of clinical studies, serving as the primary client contact and ensuring delivery in compliance with protocol, SOPs, ICH‑GCP, and regulatory requirements. You’ll shape country‑level recruitment strategies, lead feasibility and site start‑up, guide monitoring and quality strategies, and mentor CRAs and partners as we scale a new regional team. This role offers significant career growth, including opportunities to build teams, define processes, influence culture, and step into broader leadership and project management responsibilities as the region grows. 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 utilizes 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 * Support 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 * Performs 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 7 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience * Professional working proficiency in English required Preferred: * Advanced degree Other Required: * Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) * Excellent communication and interpersonal skills to effectively interface with others in a team setting * Excellent organizational skills, attention to detail, and a customer service demeanor * Ability to travel domestically and internationally including overnight stays Competencies: * Demonstrates mastery knowledge of ICH-GCP, relevant Precision SOPs, and regulatory guidance, as well as the ability to implement * Working knowledge of clinical management techniques and tools * Direct work experience in a cross-functional environment * Proven experience in functional management including proven experience in delegating while fostering cohesive team dynamics * Proven experience in 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 team * Ability to create an environment where employees have a sense of ownership that will lead to increases in productivity and efficiency * Results oriented, accountable, motivated and flexible * Excellent time management, negotiation, critical thinking, decision making, analytical and interpersonal skills * Excellent presentation, verbal and written communications skills * In depth proven experience in pharmaceutical and/or device research required * Demonstrated successful independent negotiation and conflict management strategies ### #LI-AG2 #LI-REMOTE 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. Show more [Apply now >](https://jobicy.com/jobs/148626-clinical-trial-manager-latam.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. ## How to apply ## See a few more Similar Project Management remote jobs * ![IQVIA logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/08/1eedf5ea-221.png) IQVIA ### [Project Management Analyst in Mexico, Argentina and Brazil](https://jobicy.com/jobs/148629-project-management-analyst-in-mexico-argentina-and-brazil.md) Project Management Analysts (PMA) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The PMA… ![Brazil flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/br.svg) ![Mexico flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/mx.svg) BR, MX +1 more, AR•Full TimeNEW* ![NVIDIA logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/52745899-221.jpeg) NVIDIA ### [Senior Customer Technical Program Manager – AI Datacenter](https://jobicy.com/jobs/148312-senior-customer-technical-program-manager-ai-datacenter.md) We’re looking for a Senior Customer Program Manager to lead the charge on technical programs for some of NVIDIA’s most strategic partners to build exceptional customer relationship. As a core… ![USA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/us.svg) US•Full TimeUSD 168k-322k/year* ![ManTech logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/265c7fe8-221-1.png) ManTech ### [Project Manager](https://jobicy.com/jobs/148210-project-manager-3.md) General information Requisition # R69004 Locations USA-Remote Work Posting Date 06/29/2026 Security Clearance Required None Remote Type Fully Remote Time Type Full time Description & Requirements Shape the future of… ![USA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/us.svg) US•Full TimeUSD 89,100-148,200/year* ![Testlio logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/11024036-221.png) Testlio ### [Director, Delivery (EMEA)](https://jobicy.com/jobs/148107-director-delivery-emea.md) About the jobTestlio’s fully managed crowdsourced testing platform, powered by our proprietary intelligence technology – LeoAI EngineTM, integrates expert, on-demand testers directly into your release process. Ship faster and more… ![EMEA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/emea.svg) EMEA•Full TimeJun 30* ![Nebius logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2026/06/d90c0566-221.webp) Nebius ### [Technical Program Manager, Data Centers](https://jobicy.com/jobs/148058-technical-program-manager-data-centers.md) About Nebius: Nebius is leading a new era in cloud infrastructure for the global AI economy. We are building a full-stack AI cloud platform that supports developers and enterprises from… ![Europe flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/eu.svg) ![Netherlands flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/nl.svg) EU, NL•Full TimeJun 29* ![NECSWS logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/09/4e596ed9-221.png) NECSWS ### [Project Manager – Public Safety](https://jobicy.com/jobs/145884-project-manager-public-safety-2.md) Company DescriptionCome join us and make a difference in the world!Discover more at www.necsws.comJob DescriptionWithin our Public Safety division, we provide mission‑critical systems to Emergency Services across the UK, leveraging our… ![UK flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/gb.svg) GB•Full TimeJun 18* ![APTIM logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/a3c4f002-221-1.png) APTIM ### [Project Specialist– emobility/ebike Programs](https://jobicy.com/jobs/147040-project-specialist-emobility-ebike-programs.md) Job Overview:APTIM Energy Transition team is seeking a Project Specialist who will be a customer service representative for our portfolio of E-bike Rebate Programs and new e-mobility programs with APTIM…. ![USA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/us.svg) US•Full TimeJun 17* ![CodePath logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2026/06/58acdc3a-221.webp) CodePath ### [Engineering Project and QA Manager](https://jobicy.com/jobs/146796-engineering-project-and-qa-manager.md) CodePath is an AI-native organization building pathways into tech for the next generation of engineers, CTOs, and founders. We deliver industry-vetted technical courses and programs to learners across the country…. ![USA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/us.svg) ![Canada flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/ca.svg) US, CA +2 more, EU, LATAM•Full TimeUSD 140k-178k/year* ![World Wide Technology logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/c0d2c26d-221.png) World Wide Technology ### [Service Delivery Manager – D2Ops](https://jobicy.com/jobs/146381-service-delivery-manager-d2ops.md) Qualifications 5+ years of Incident Management, Problem Management, or Crisis Management experience required Exposure to technology projects and project management Advanced Skills in MS Office applications including Excel, Work, and… ![USA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/us.svg) US•Full TimeUSD 85k-100k/year* ![World Wide Technology logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/c0d2c26d-221.png) World Wide Technology ### [Sr. Technical Delivery Manager (East Region)](https://jobicy.com/jobs/146377-sr-technical-delivery-manager-east-region.md) Qualifications Required Must be located in the central, southern, or eastern region Must have experience delivering financial services projects and have recent partnerships within the global finance industry 12+ years of… ![USA flag](https://cloud.jobicy.com/nyc4-cold/img/round-flags/us.svg) US•Full TimeUSD 190k-220k/year [More Jobs](https://jobicy.com/jobs.md)