Asistente de Investigación Clínica - Puebla

Placements24; Puebla de Zaragoza; Presencial; MXN 180 000 - 240 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health benefits

Retirement plan

Paid time off

Training and career development

Resumo da oferta

Placements24 is seeking a diligent Clinical Research Assistant to support our client’s trials in Puebla, Mexico. The role focuses on administrative and operational tasks, managing documents, coordinating visits, and ensuring data integrity with the team.

The ideal candidate will have at least a high school diploma, basic clinical trial knowledge, and strong organization. This on-site position offers health benefits, professional development, and a collaborative environment.

Qualificações

• High school diploma required; associate or bachelor's preferred.
• Experience in clinical research or healthcare setting is advantageous.
• Understanding of medical/clinical trial terminology.
• Familiarity with GCP and regulatory requirements.
• Proficiency in MS Office (Word, Excel, Outlook, PowerPoint).
• Excellent organizational skills and ability to multitask.
• Strong written and verbal communication; Spanish fluency essential.
• Ability to work on-site full-time in Puebla, Mexico.

Responsabilidades

• Assist Coordinators and investigators in managing study documents and regulatory binders.
• Schedule patient visits and coordinate study-related appointments.
• Collect, organize, and maintain case report forms and source documents.
• Ensure compliance with study protocols, SOPs, and GCP guidelines.
• Assist with participant recruitment and screening processes as directed.
• Prepare study materials and equipment for site initiation and monitoring visits.
• Communicate effectively with study participants, staff, and external stakeholders.
• Data entry and query resolution in clinical databases.

Conhecimentos

Organizational skills

Attention to detail

Communication skills

Teamwork

Spanish fluency

English proficiency

MS Office

Formação académica

High School Diploma

Associate's or Bachelor's degree in a relevant field

Descrição da oferta de emprego

About the Role

Our client, a prominent pharmaceutical organization dedicated to advancing medical research, is actively seeking a diligent and organized Asistente de Investigación Clínica to support their clinical trial operations based in Puebla, Puebla . This crucial role involves providing essential administrative and operational support to the clinical research team, ensuring the smooth execution of studies. The ideal candidate will possess excellent organizational skills, a keen eye for detail, and a foundational understanding of clinical trial processes. You will play a key part in facilitating research that leads to the development of new therapies. This is an excellent opportunity for an individual looking to build a career in clinical research within a supportive and professional environment located in Puebla . The role requires full-time dedication on-site to effectively manage study documentation and participant interactions.

Key Responsibilities

• Assist Clinical Research Coordinators (CRCs) and investigators in managing study-related documents and regulatory binders.
• Schedule patient visits and coordinate study-related appointments.
• Collect, organize, and maintain accurate and complete case report forms (CRFs) and source documents.
• Ensure compliance with study protocols, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
• Assist with participant recruitment and screening processes as directed.
• Prepare study materials and equipment for site initiation and ongoing monitoring visits.
• Communicate effectively with study participants, research staff, and external stakeholders.
• Perform data entry and assist with data query resolution in clinical databases.
• Maintain the confidentiality and security of all study-related information and participant data.
• Provide general administrative support to the clinical research team, including filing, copying, and managing supplies.

Requirements

• High school diploma required; Associate's or Bachelor's degree in a relevant scientific or healthcare field is preferred.
• Previous experience in a clinical research setting or healthcare environment is a significant advantage.
• Understanding of basic medical terminology and clinical trial terminology.
• Familiarity with GCP guidelines and regulatory requirements for clinical trials is a plus.
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint).
• Excellent organizational skills, attention to detail, and ability to manage multiple tasks simultaneously.
• Strong interpersonal and communication skills, both written and verbal.
• Ability to work effectively as part of a team and independently when required.
• Reliability, strong work ethic, and a commitment to patient safety and data integrity.
• Fluency in Spanish is essential; basic English proficiency is beneficial.

Benefits

Our client offers a competitive starting salary, comprehensive health benefits package, including medical, dental, and vision coverage, and a retirement savings plan. Paid time off and opportunities for on-the-job training and career advancement within the clinical research field are provided. Join our dedicated team in Puebla and contribute to the vital work of bringing new medicines to patients.