Regulatory Submissions Expert for Clinical Trials

IQVIA Inc; Tandil; On-site; ARS 77,270,000 - 123,632,000; Full time

Job summary

IQVIA is seeking a Regulatory Affairs professional to prepare and/or review regulatory submissions documents supporting clinical trial and marketing authorization activities for internal and external clients. The role involves collaborating with senior staff, managing timelines, and delivering regulatory documentation with a focus on quality and compliance.

Ideal candidates have 2–3 years in Regulatory Affairs, fluent English, and a solid understanding of the R&D process, CMC, MA transfers,

Qualifications

• Bachelor's degree in Lifescience or related discipline.
• Master's degree in Lifescience or related discipline is a plus.
• 2–3 years relevant experience in Regulatory Affairs in general, Publishing, Word Formatting, Clinical PDF Publishing, Submission Publishing activities.
• Fluent English (writing, speaking, reading).
• Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines.
• 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.
• Demonstrates self-motivation and enthusiasm.
• Ability to work on several projects, with direction from senior staff as appropriate.
• Ability to follow standard operating porcedures 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.

Responsibilities

• 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.

Skills

Fluent English

Interpersonal skills

Organizational skills

Independent working

Education

Bachelor's Degree in Lifescience

Master's Degree in Lifescience

Tools

Microsoft Office

Job description

IQVIA is seeking a Regulatory Affairs professional to prepare and/or review regulatory submissions documents supporting clinical trial and marketing authorization activities for internal and external clients. The role involves collaborating with senior staff, managing timelines, and delivering regulatory documentation with a focus on quality and compliance.

Ideal candidates have 2–3 years in Regulatory Affairs, fluent English, and a solid understanding of the R&D process, CMC, MA transfers,