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Regulatory Affairs Officer, IQVIA Biotech
IQVIA —Buenos Aires, Buenos Aires
Public Health Advisor
US Food and Drug Administration —Buenos Aires, Buenos Aires
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Regulatory Affairs Officer, IQVIA Biotech
IQVIA —Buenos Aires, Buenos Aires
3–4 years of relevant clinical trial regulatory experience within CRO or biotech/pharma. Bachelor’s or Master’s degree in Life Sciences or related discipline.
Medical Monitor, Rheumatology, Canada or Argentina
Indero —Desde casa
Escalate to the Project Manager or Sponsor any issues requiring medical input and significant safety or data integrity concerns identified during review of data…
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Regulatory Affairs Officer, IQVIA Biotech

IQVIA -
Buenos Aires, Buenos Aires

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Detalles del empleo

Descripción completa del empleo

Key Responsibilities

Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing.

Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level .

Engage directly with clients to clarify clinical trial regulatory pathways, share lessons learned, and address feedback.

Engage with Competent Authorities in countries across multiple regions, as part of the clinical trial regulatory strategy for complex global studies

Monitor scope, deliverables, timelines, and budget; proactively mitigate risks and escalate issues as needed.

Provide guidance and feedback to junior colleagues; support training and continuous improvement initiatives.

Contribute to internal SOP reviews and present regulatory processes at full-service bid defenses.

Perform additional tasks assigned by Regulatory management to meet program goals.

Qualifications

Bachelor’s or Master’s degree in Life Sciences or related discipline.

3–4 years of relevant clinical trial regulatory experience within CRO or biotech/pharma.

Strong understanding of the R&D continuum (CMC, preclinical, clinical) and applicable laws, guidelines, and agency expectations for clinical trials.

Demonstrated expertise in at least one clinical trial regulatory domain (e.g., CMC, labeling).

Experience with clinical trial regulatory submission platforms and pathways, including but not limited to, EU CTR, Health Canada, US FDA IND submissions and/or systems in other regions such as LATAM or APAC. Biotech therapy area exposure welcomed.

Proficiency with Microsoft Office and regulatory publishing tools (e.g., eCTD systems); meticulous document management skills.

Excellent written and verbal communication, organization, and stakeholder-management abilities.

Proven ability to manage multiple projects; work in a fast-paced environment with competing priorities; and view obstacles as challenges to be handled with ease and grace; follow SOPs consistently, and exercise sound judgment on discrete tasks.

Problem-solving mindset with adaptability in fast-changing environments; self-motivated and collaborative.

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.

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Regulatory Affairs Officer, IQVIA Biotech

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