Sr Site Activation Analyst

MSC Quintiles Mexico S. de R.L. de C.V.; Ciudad de México; Presencial; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A clinical research organization in Mexico City is seeking a candidate for site activation activities in clinical research. Responsibilities include document preparation, feasibility evaluations, and maintaining project-specific information. Qualified candidates should have a Bachelor's Degree in Life Science and at least 1 year of relevant experience. Fluency in conversational English is required.

Formación

• Minimum 1 year of experience in site activation activities in clinical research.
• Ability to prepare and review site documents for accuracy.

Responsabilidades

• Perform feasibility, site activation and maintenance activities.
• Review documents for completeness, consistency, and accuracy.
• Support update and maintenance of internal systems and databases.

Conocimientos

Fluent conversational English

Attention to detail

Educación

Bachelor's Degree in Life Science or related field

Descripción del empleo

Job Overview

Under general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities.

Essential Functions

• Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare site documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory contractual and other documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
• Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications

• Bachelor's Degree in Life Science or related field.
• At least 1 year of experience in site activation activities in clinical research.

Fluent conversational English.