Senior In-house CRA – LATAM

This is a fully remote position, open to applicants in Mexico.

📋 Description

• Provides comprehensive support to clinical project teams and study sites engaged in clinical research studies.

• Complies with relevant protocols, standard operating procedures (SOPs), and all applicable guidelines and regulatory requirements.

• Serves as the primary point of contact for study sites.

• Coordinates internal and external meetings as necessary.

• Prepares and distributes Investigator Site Files to study sites.

• Conducts ongoing collection, review, maintenance, and close-out activities for essential documents.

• Aids in investigator recruitment efforts by utilizing phone scripts, questionnaires, and study site materials.

• Ensures prompt and accurate data entry by the site in EDC or other systems requiring data input.

• May act as an Independent Essential Document Reviewer post-SIV by assisting with on-site visit activities.

⛳️ Requirements

• Bachelor's degree or international equivalent, or a relevant combination of education and experience, preferably in a business, scientific, or healthcare field.

• A minimum of 4 years of experience in clinical trials or related areas.

• High proficiency in Microsoft Office applications (Outlook, Word, Excel, and PowerPoint).

• Excellent verbal and written communication skills in English.

• Thorough understanding of the drug development process.

• Experience with CTMS, TMF, and EDC systems.

• Willingness to travel as needed.

🏝️ Benefits

• Health insurance.

• Customer service-oriented demeanor; exemplifies flexibility and teamwork.

• Opportunities for professional development.