Regulatory Affairs Officer

IQVIA; Bogotá ciudad; Presencial; COP 26.000.000 - 42.000.000; Jornada completa

Descripción de la vacante

IQVIA in Bogotá seeks a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorizations. You will support project timelines and collaborate with internal and external clients on regulatory activities.

The role requires a Lifescience degree, 2+ years in regulatory affairs, English fluency, and strong communication skills. Knowledge of US/Canada processes is a plus, with opportunity to grow in a global team.

Formación

• Bachelor’s Degree in Lifescience or related discipline.
• At least 2 years of regulatory affairs (postmarketing) experience.
• 1 year tracking information on regulatory processes.
• Fluent English: Spoken, Read and Written.
• Nice to have worked with USA or Canada.

Responsabilidades

• Prepare and/or review regulatory submissions documents.
• Support regulatory activities and project timelines.
• Participate in project teams and communicate with clients.
• Assist in process improvements and SOP adherence.

Conocimientos

Regulatory knowledge

Project coordination

Communication skills

Microsoft Office

Team collaboration

English fluency

Educación

Bachelor’s Degree in Lifescience

Herramientas

Microsoft Office

Publishing tools

Descripción del empleo

Job Overview

Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects.

Essential Functions

• Acts as a Regulatory Team Member on small, straightforward regulatory projects and/or gets involved in a small single service project, under the guidance of senior staff;
• Identifies project needs, tracks project timelines, implements client requests and manages day-to-day workload in collaboration with senior staff, as appropriate;
• Experienced in Regulatory knowledge in Chemistry, Manufacturing and Controls/ Lifecycle Maintenance/ Marketing Authorization Transfers/ Labeling/ Publishing as applicable;
• Prepares and/or reviews regulatory documentation in area of expertise, as appropriate;
• Actively participates in project teams with internal and external customers independently and communicates confidently in straightforward matters;
• Understands the Scope of Work, deliverables for any given project;
• May prepare slides and background material for small, straightforward business development meetings under senior guidance and presents in client meetings by phone or in person;
• May prepare and deliver trainings, as appropriate;
• Performs other tasks or assignments, as delegated by Regulatory management;
• Responsible for making minor changes in systems and processes to solve problems where problems faced are not typically difficult or complex;

Qualifications

• Bachelor’s Degree in Lifescience or related discipline.
• At least 2 years of regulatory affairs (postmarketing) experience: maintenance records, new records, regulatory activities.
• 1 year tracking information on regulatory processes.
• Fluent English: Spoken, Read and Written.
• It’s a plus to have worked with other countries: USA, Canada.
• Good, solid interpersonal communication (oral and written) and organization skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Strong software and computer skills, including Microsoft Office , publishing applications and tools, as applicable.
• Demonstrates self-motivation and enthusiasm.
• Ability to work on several projects, with direction from senior staff as appropriate.
• Ability to follow standard operating procedures consistently; provides independent thought to assist in process improvements.
• Ability to make decisions on discrete tasks under senior supervision.
• Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education.
• Makes adjustments or recommended enhancements in systems and processes to solve problems or improve effectiveness of job area.
• Problems faced are general and may require understanding of broader set of issues, but typically are not complex.
• Applicable certifications and licenses as required by country, state, and/or other regulatory bodies.

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.