Principal In-house CRA – LATAM

Precision For Medicine

Principal In-house CRA providing support for clinical research across Mexico, Brazil, Argentina, Colombia, Chile, and Peru. Managing trial activities and site interactions to ensure compliance with regulations.

Posted 6/26/2026full-timeRemote • 🇲🇽 MexicoLeadWebsite

About the role

Key responsibilities & impact

We’re expanding across Mexico, Brazil, Argentina, Colombia, Chile, and Peru.
The Principal In-house CRA provides overall support to study sites and clinical project teams engaged in clinical research studies.
Adheres to applicable protocols, standard operating procedures (SOPs) and all applicable guidelines and regulatory requirements.
Acting as point of contact for study sites.
Has extensive site management experience which included experience and knowledge across different type of projects.
Responsible for providing senior oversight and act as subject matter expert in site management activities.
Acting as resource for Clinical Monitoring management team support and mentoring and developing others in the team.
Performs and manages investigator recruitment activities and assists with development of tools such as phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites in partnership with study team.
Schedules internal and external meetings as required.
Prepares Investigator Site Files including distribution to study sites (electronically or physically), coordination with shipping vendor, if required.
Performs ongoing essential document collection and review, maintenance, and close-out activities, organizing and maintaining site level data in the trial master file (TMF).
Assist with sets up and maintains site-related data in applicable clinical systems according to procedures and guidelines.
Ensures timely and complete data entry by site in EDC or any other system that requires data entry.
Sends email blasts/newsletter, updates, and updated study core documents to study site personnel.

Requirements

What you’ll need

Bachelor's degree / international equivalent or equivalent combination of education and experience ideally in a business, scientific or healthcare discipline
6 years of clinical trial or related experience
High in proficiency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint).
Customer service demeanor; demonstrate flexibility and teamwork
Ability to focus on detail for extended periods of time, high attention to accuracy
Fluency in English communication, verbally and in writing
In-depth knowledge of the drug development process
Experienced with utilizing CTMS, TMF, and EDC systems
Ability to travel as needed.

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work hours
Paid time off
Remote work options

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial experiencesite managementinvestigator recruitmentdata entrydocument collectionattention to detaildrug development processclinical researchstudy site materials developmentmentoring

Soft Skills

customer serviceflexibilityteamworkcommunicationaccuracyorganizational skillsleadershipproblem-solvingtime managementinterpersonal skills