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 idóneo 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.

📌 Asistente de Investigación Clínica (Heroica Puebla de Zaragoza)
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📍 Heroica Puebla de Zaragoza