Remote opportunity at
pfm medical, inc.Senior Clinical Trial Manager (LATAM)
pfm medical, inc. is hiring a Senior Clinical Trial Manager (LATAM) to build and lead expanding clinical operations across multiple countries in Latin America, including Mexico,…
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About This Role
pfm medical, inc. is hiring a Senior Clinical Trial Manager (LATAM) to build and lead expanding clinical operations across multiple countries in Latin America, including Mexico, Brazil, Argentina, Colombia, Chile, and Peru. This remote, full-time position acts as the main clinical point of contact for clients and involves managing the planning, execution, and oversight of clinical studies in compliance with study protocols, standard operating procedures, ICH-GCP, and regulatory guidelines. This…
Job Description
pfm medical, inc. is hiring a Senior Clinical Trial Manager (LATAM) to build and lead expanding clinical operations across multiple countries in Latin America, including Mexico, Brazil, Argentina, Colombia, Chile, and Peru. This remote, full-time position acts as the main clinical point of contact for clients and involves managing the planning, execution, and oversight of clinical studies in compliance with study protocols, standard operating procedures, ICH-GCP, and regulatory guidelines.
This role suits an experienced clinical research professional ready to shape regional recruitment strategies, manage study start-ups, mentor clinical research associates and third-party partners, and drive quality strategies. Responsibilities include generating potential site lists, conducting feasibility analyses, coordinating IRB and ethics committee submissions, overseeing electronic trial master file implementation, and assisting with audit preparations. Depending on program needs, the position may also assume project management duties, support business development, negotiate site budgets, and handle vendor management.
Responsibilities
- Serve as the primary clinical contact for clients and lead internal clinical team meetings
- Collaborate with project managers on monthly invoicing and clinical budget variance management
- Create study-related clinical documents, training materials, and tracking tools
- Drive the site feasibility process, identify enrollment risks, and develop recruitment and retention strategies
- Oversee submissions and approvals to competent authorities, IRBs, and ethics committees
- Develop clinical monitoring strategies and utilize metrics reporting to ensure study adherence
- Manage the electronic trial master file and support CAPA implementation and closure
- Collaborate with data management and clinical research associates to ensure data quality and cleaning compliance
- Manage investigational product processes, including drug accountability and reconciliation
Requirements
- Minimum of 7 years of clinical research experience or proven competencies for the role, with significant clinical monitoring experience
- In-depth proven experience in pharmaceutical and/or device research
- Professional working proficiency in English
- Proficiency in Microsoft Office products including Outlook, Word, Excel, and PowerPoint
- Legal authorization to work in the country of employment without employer sponsorship
Qualifications
- Bachelor's degree or equivalent combination of education and experience in a science or health-related field
- Advanced degree
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the source posting lists the remote status as remote.
What is the employment type?
The position is full-time.
What is the salary for this role?
The source posting does not specify a salary.
What education or experience is required?
Candidates must have a minimum of 7 years of clinical research experience or proven competencies with significant clinical monitoring experience, along with in-depth experience in pharmaceutical or device research. A bachelor's degree or equivalent in a science or health-related field is required, while an advanced degree is preferred.
Sample Interview Questions
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