Lead Clinical Research

Pharmaceutical Research Associates, Inc; Ciudad de México; Presencial; MXN 400,000 - 600,000; Jornada completa

Descripción de la vacante

A leading clinical research organization in Mexico City is seeking a Site Management Liaison to manage clinical deliverables, provide training, and ensure regulatory compliance. The ideal candidate has a Bachelor's degree in health or life sciences and 3+ years of experience in the pharmaceutical industry or clinical research. This role involves communication with project teams and risk management. Competitive salary and benefits offered.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Formación

• Minimum of 3 years experience in the pharmaceutical industry or clinical research.
• Strong working knowledge of Good Clinical Practice.
• Equivalent combination of education, training, and relevant experience may be considered.

Responsabilidades

• Manage clinical deliverables to meet quality and regulatory requirements.
• Create and administer clinical and site training plans.
• Recognize potential risks and establish contingency plans.
• Communicate effectively with all project team members.

Conocimientos

Fluent English

Knowledge of Good Clinical Practice

Project Management

Educación

Bachelor’s degree in a health or life sciences

Descripción del empleo

Overview

As a Site Management Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be joining one of the global healthcare leaders that has been discovering and developing medicines and treatments for well over a century. You will be part of a global team that is committed to make life better for people around the world. We share a vision of bringing treatment and medicine to millions alongside develop healthcare knowledge and improve live.

Responsibilities

What you will be doing:

• Manages and prioritizes the clinical deliverables to ensure that deliverables meet quality and regulatory requirements, project timelines, budget, and sponsor expectations.
• Creates and administers clinical and site training plans. Ensures clinical team understands responsibilities and performance standards.
• Recognizes potential risks within the study protocol and operational aspects of the trial; proactively establishes contingency and mitigation plans.
• Ensures that quality standards and applicable regulatory requirements are met. Facilitates internal audits and local health authority inspections as needed.
• Communicates effectively with sponsor, project manager, functional team leads and other project team members. Leads clinical study team meetings.
• Provides training and guidance to clinical study team members.

Qualifications

You are:

• Bachelor’s degree in a health, life sciences or other relevant field of study

• Minimum of 3 years experience in the pharmaceutical industry and/or clinical research and strong working knowledge of Good Clinical Practice

• Occasional travel as needed.

• Exposure to the clinical research environment as a SEL, medical science liaison (MSL), study coordinator, Senior CRA or experience in a CRO

• All employees must read, write and speak fluent English and host country language.

• Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above.

What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.