Remote opportunity at
Precision Medicine GroupSenior Clinical Trial Manager (LATAM)
Precision Medicine Group is hiring a Senior Clinical Trial Manager to oversee and expand clinical operations throughout Latin America, specifically focusing on growth in Mexico, Brazil,…
Career Tools
About This Role
Precision Medicine Group is hiring a Senior Clinical Trial Manager to oversee and expand clinical operations throughout Latin America, specifically focusing on growth in Mexico, Brazil, Argentina, Colombia, Chile, and Peru. This position serves as the primary clinical point of contact for clients, managing the complete lifecycle of clinical studies from planning and site start-up to execution and close-out. The chosen professional will drive regional enrollment strategies, lead site feasibility,…
Job Description
Precision Medicine Group is hiring a Senior Clinical Trial Manager to oversee and expand clinical operations throughout Latin America, specifically focusing on growth in Mexico, Brazil, Argentina, Colombia, Chile, and Peru. This position serves as the primary clinical point of contact for clients, managing the complete lifecycle of clinical studies from planning and site start-up to execution and close-out. The chosen professional will drive regional enrollment strategies, lead site feasibility, guide monitoring quality, and mentor Clinical Research Associates as the local team scales.
This role suits an experienced clinical research professional with a background in pharmaceutical or device trials who excels in cross-functional environments and functional management. Responsibilities include financial tracking, regulatory submissions, electronic Trial Master File management, and ensuring adherence to protocol and compliance standards. Candidates must be prepared to handle both independent project oversight and collaborative leadership duties as regional activities expand.
Responsibilities
- Act as the primary clinical point of contact for clients and collaborate with project managers on monthly invoicing and budget variance management
- Create study-related clinical documents such as manuals, informed consent templates, tracking sheets, and training materials
- Drive the site feasibility process, generate potential site lists, and formulate recruitment and retention strategies
- Lead internal clinical team meetings and set performance expectations for clinical research associates and clinical trial assistants
- Oversee submissions and approvals involving competent authorities, institutional review boards, and ethics committees
- Manage electronic Trial Master File implementation and ensure ongoing quality and protocol compliance
- Partner with data management and clinical research associates to guarantee data quality and maintain clean data timelines
- Handle investigational product processes, including drug accountability, reconciliation, and release package reviews
- Assist with Corrective and Preventative Action Plan development, implementation, and timely closure
- Assume project management duties, negotiate site budgets, or manage clinical vendors when necessary
Requirements
- Minimum of seven years of clinical research experience or proven competencies for the position
- Significant background in clinical monitoring
- In-depth proven experience in pharmaceutical or device research
- Direct work experience operating in a cross-functional environment
- Demonstrated expertise in functional management, delegation, and fostering team dynamics
- Proficiency with Microsoft Office software including Outlook, Word, Excel, and PowerPoint
- Professional working proficiency in English
- Mastery knowledge of ICH-GCP, relevant standard operating procedures, and regulatory guidance
- Legal authorization to work in the country of employment without employer sponsorship
- Ability to travel domestically and internationally, including overnight stays
Qualifications
- Bachelor’s degree or equivalent combination of education and experience in a science or health-related field
- Advanced degree in a science or health-related field
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
What is the remote work policy for this role?
The source posting indicates that the position is remote.
What is the employment type?
The position is a full-time role.
What salary is offered for this position?
The salary is not stated in the job posting.
What education level is required?
A bachelor’s degree or an equivalent combination of education and experience in a science or health-related field is required, with an advanced degree preferred.
Sample Interview Questions
AI-generated questions tailored to this specific role — a preview of the full practice set.
Related Jobs