11 publicaciones de empleo destacadas en java engineer remote, within eu (¡Están contratando!)

Regulatory Affairs Officer, IQVIA Biotech
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
7d
Senior Salesforce Platform Architect
サイネオス・ヘルス —Buenos Aires, Buenos Aires
Sr Tech Customer Success Analyst
サイネオス・ヘルス —Buenos Aires, Buenos Aires
Growth Strategy Analyst
FeverUp —Capital Federal, Buenos Aires
Postulación rápida
Senior Account Executive
FeverUp —Capital Federal, Buenos Aires
Postulación rápida
Growth Strategy Manager
FeverUp —Buenos Aires, Buenos Aires
Postulación rápida
14d
Performance Marketing Specialist, Mobile
Blockchain.com —Buenos Aires, Buenos Aires
Postulación rápida
Growth Strategy Senior Analyst
FeverUp —Capital Federal, Buenos Aires
Postulación rápida
Site Contracts Specialist with clinical trials experience Home-Based in Argentina
サイネオス・ヘルス —Buenos Aires, Buenos Aires
8d
Media Manager (Traditional Media)
FeverUp —Capital Federal, Buenos Aires
Postulación rápida
Pharmacovigilance - Project Manager
Med Communications International —Buenos Aires, Buenos Aires
- Tiempo completo
Postulación rápida
2h

Related jobs to explore

Based on your search for java engineer remote, within eu

FLS Support Engineer - South America
Connected Manufacturing™ —Desde casa
Milestone delivery or hypercare periods. B.S. degree in Information Technology, or Associates degree in Computer Science or related Field (or the equivalent…
Postulación rápida
Front End Engineer - Remote
EventMobi —Buenos Aires, Buenos Aires
Contribute to features within our Progressive Web App. Interest in mobile or cross-platform development. Familiarity with CI/CD workflows or cloud environments.

Quiero recibir la alerta de empleo más reciente para java engineer remote, within eu

Al ingresar a tu cuenta, aceptas las Condiciones del servicio de SimplyHired y das tu consentimiento a nuestra Política de privacidad y Cookies.

Regulatory Affairs Officer, IQVIA Biotech

IQVIA -
Buenos Aires, Buenos Aires

Postulate ahora

Detalles del empleo

Tiempo completo
Hace 7 días

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Home-based | R1550155

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.

Postulate ahora

Refiná tu búsqueda

java engineer remote, within eu empleos

Regulatory Affairs Officer, IQVIA Biotech

Senior Salesforce Platform Architect

Sr Tech Customer Success Analyst

Growth Strategy Analyst

Senior Account Executive

Growth Strategy Manager

Performance Marketing Specialist, Mobile

Growth Strategy Senior Analyst

Site Contracts Specialist with clinical trials experience Home-Based in Argentina

Media Manager (Traditional Media)

Pharmacovigilance - Project Manager

Related jobs to explore

Quiero recibir la alerta de empleo más reciente para java engineer remote, within eu

Related Searches

Herramientas para candidatos

Herramientas para empresas

Explorar

Mantente conectado