In-House CRA II

Puesto: In-House CRA II )
We’re expanding across

Mexico, Brazil, Argentina, Colombia, Chile and Peru , and we’re looking for an experienced In-house CRA II to help build the foundation of this new regional function in LATAM!

The In-house CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies. You will adhere to applicable protocols, standard operating procedures (SOPs) and all applicable guidelines and regulatory requirements (e.g., International Council for Harmonization (ICH), Good Clinical Practice (GCP), and country/region-specific regulations). Acts as point of contact for study sites.

The In-house CRA ll is a solid team member who can execute all core responsibilities consistently across several studies using independent judgment and critical thinking. Individual works independently as study team member with minimum support in complex activities.

Essential functions of the job included but not limited to:

Assist with the investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites

May assist in identifying study sites by performing site feasibility and recruitment tasks, e.g., completing, disseminating, and reviewing responses to site recruitment questionnaires

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) under general supervision ensuring that sponsor and investigator obligations are being met and are compliant with ICH/GCP guidelines and applicable local regulations

Assist with set ups and maintains site-related data in applicable clinical systems according to procedures and guidelines Utilizes the Clinical Trial Management System (CTMS) to ensure milestones and activities are accurately tracked

Acts as site contact/liaison for study and site management issues including addressing questions, assists with managing study supplies, and may support offsite central monitoring activities. Escalates issues and risks as needed

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

Assists in providing logistics support in samples management and tracking, where applicable and in study supply management

Supports investigators and investigative staff in fulfilling obligations regarding local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements

Assists in data review inclusive of site level data review, resolutions provided by sites to queries, facilitates database closure and freezing procedures as per study plans

Assist with study tracking via the CTMS, Study specific trackers or sponsor designated system to ensure that the study reporting is current, accurate and complete

Documents site and Sponsor contact and study interactions in a timely and professional manner

Assist in remote review of the electronical Investigator Site File, where applicable

Assists with Investigational Product accountability, where applicable

Consults with project team members regarding study site issues

Provides quality review of the amended site level informed consent template

Follows up with sites for trial invoices and ensures the CTMS is accurately updated to allow the timely processing of Investigator Payments

May attend site visits as needed, supporting the CRA to…