FSP - Import/Export Specialist

IQVIA Argentina; Santiago; Presencial; CLP 18.000.000 - 24.000.000; Jornada completa

Descripción de la vacante

IQVIA Argentina is seeking an Import/Export Specialist to manage LATAM import/export activities, with a Chile focus. The role ensures SOP adherence, quality of deliverables, and timely project execution. You will maintain systems and provide local expertise during project timelines.

The ideal candidate has clinical research experience, at least 1 year in international trade within the pharmaceutical industry, advanced English, and strong organizational and interpersonal skills.

Formación

• Clinical research experience. Equivalent combination of education, training, and experience.
• At least 1 year experience related to international trade (ComEx), import and export processes in pharmaceutical industry (clinical Trials)
• Advanced English level
• Good communicational and interpersonal skills
• Good organizational skills

Responsabilidades

• Handle importation and exportation activities for LATAM countries, with Chile as a focus.
• Ensure adherence to SOPs and Work Instructions, project timelines and quality Deliverables.
• Maintain internal systems, databases and tracking tools with project information.
• Plan and monitor project timelines; implement contingency plans as needed.
• Provide local expertise to SAMs and project teams during timeline planning.
• Perform quality control of documents and records.
• Interact with sponsors on initiatives and meetings as required.

Conocimientos

Good communicational skills

Advanced English

Educación

Clinical research experience or equivalent

Descripción del empleo

Import/ Export Specialist (RSU1)

Essential Functions

• Responsible for importation and exportation activities in specific LATAM countries for our FSP model. Chile - Expertise and knowledge as a plus in other LATAM countries such Argentina, Colombia, Brazil and Mexico)
• Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
• Provide local expertise to SAMs and project team (Client) during initial and on-going project timeline planning related to Importation and Exportation activities.
• Perform quality control of documents.
• May have direct contact with sponsors on specific initiatives (KOM, internal meetings, F2F meetings)

Requirements

• Clinical research experience. Equivalent combination of education, training, and experience.
• At least 1 year experience related to international trade (ComEx), import and export processes in pharmaceutical industry (clinical Trials)
• Advanced English level
• Good communicational and interpersonal skills
• Good organizational skills

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.