Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Precision For Medicine

Senior In-house CRA – LATAM

Precision For Medicine

Senior In-house CRA providing clinical research support for expanding operations in Mexico and LATAM region. Focused on building foundation through study site support and adherence to regulatory requirements.

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

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
clinical trial experiencedata entrydocument collectiondocument reviewinvestigator recruitmentMicrosoft Officedrug development process
Soft Skills
communicationorganizational skillsattention to detail
Tools & Technologies
CTMSTMFEDC
Industry Keywords
clinical researchSOPsregulatory requirementsinvestigator site files

About the role

Key responsibilities & impact
  • 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
  • Acts as a point of contact for study sites
  • Schedules internal and external meetings as required
  • Prepares Investigator Site Files including distribution to study sites
  • Performs ongoing essential document collection and review, maintenance, and close-out activities
  • Assists with the investigator recruitment activities utilizing phone scripts, questionnaires, study site materials
  • Ensures timely and complete data entry by site in EDC or any other system that requires data entry
  • May serve as an Independent Essential Document Reviewer post-SIV by supporting on-site visit activities

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
  • 4 years of clinical trial or related experience
  • High in proficiency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint)
  • 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
  • Customer service demeanor; demonstrate flexibility and teamwork
  • Professional development opportunities