Farmacéutico de Investigación Clínica y Desarrollo de Protocolos

Placements24; Cuernavaca; Hybrid; MXN 344,000 - 551,000; Full time

Benefits offered by this job

Remote work arrangement

Professional development and networks

Job summary

Placements24 is seeking a detail-oriented Farmacéutico de Investigación Clínica near Cuernavaca, Morelos, to support clinical trial design and execution. You will review study designs for pharmaceutical robustness and collaborate with investigators to ensure drug-specific considerations are met.

The role requires a PharmD or Licenciatura in Pharmacy, at least 2 years in clinical research or hospital/pharma settings, and strong knowledge of IP management and GCP guidelines.

Qualifications

• 2+ years in clinical research, hospital pharmacy, or pharma industry.
• Familiar with clinical trial processes and GCP guidelines.
• Strong written and verbal communication.

Responsibilities

• Review protocols for feasibility and pharmaceutical implications.
• Assist IP management, dispensing, and accountability procedures.
• Collaborate with sponsors, investigators and site personnel on queries.
• Ensure compliance with GCP and regulatory guidelines for IP handling.
• Contribute to drug supply strategy design (packaging, labeling, distribution).
• Prepare and review essential documents for IP handling.

Skills

Clinical trials

GCP knowledge

Pharmaceutical terminology

MS Office

Independent work

Education

Pharmacist degree (PharmD)

Job description

About the Role

Our client, a dynamic Contract Research Organization (CRO) with a presence near Cuernavaca, Morelos , is seeking a detail-oriented Farmacéutico de Investigación Clínica to contribute to the development and execution of clinical trial protocols. This role involves reviewing study designs, ensuring pharmaceutical aspects of trials are robust, and collaborating with investigators and study teams. The ideal candidate will have a solid understanding of clinical research principles and pharmaceutical science. This contract position offers an excellent opportunity to engage in cutting-edge research and gain valuable experience in the pharmaceutical industry.

Key Responsibilities

• Review clinical trial protocols to assess feasibility, clarity, and pharmaceutical implications.
• Assist in the development of study-specific procedures related to investigational product (IP) management, dispensing, and accountability.
• Collaborate with study sponsors, investigators, and site personnel to address pharmaceutical-related queries during clinical trials.
• Ensure compliance with Good Clinical Practice (GCP) and relevant regulatory guidelines pertaining to investigational drugs.
• Contribute to the design of drug supply strategies, including packaging, labeling, and distribution plans.
• Prepare and review essential documents related to investigational product handling.
• Provide training to site staff on the proper handling and administration of investigational medicinal products.
• Monitor study progress and identify potential risks or issues related to pharmaceutical aspects.
• Stay updated on regulatory requirements and best practices in clinical trial conduct and pharmaceutical management.
• Assist in the preparation of reports and documentation for regulatory submissions.

Requirements

• Licenciatura en Farmacia or Doctor of Pharmacy (PharmD) degree.
• Minimum of 2 years of experience in clinical research, hospital pharmacy, or pharmaceutical industry, with exposure to clinical trials.
• Good understanding of clinical trial processes and Good Clinical Practice (GCP) guidelines.
• Knowledge of pharmaceutical terminology, drug classifications, and dosage forms.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills.
• Ability to work independently and manage multiple tasks effectively in remote setting.
• Proficiency in MS Office (Word Excel PowerPoint).
• Familiar of investigational product management is plus.

Benefits

This contract position offers a competitive hourly rate and the flexibility of a remote work arrangement. You will gain invaluable experience working with a professional CRO on diverse clinical research projects, contributing to the development of new therapies. Opportunities for professional development and networking within the clinical research field are available. Be part of exciting research initiatives impacting healthcare from your home base, with potential for collaboration with teams operating near Cuernavaca, Morelos .