17 publicaciones de empleo destacadas de data entry en martínez, b (¡Están contratando!)

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- Tiempo completo
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Sr. E-commerce Accountant
Latino Legends —Buenos Aires, Buenos Aires
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Howard —Capital Federal, Buenos Aires
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Loyalty Partner Insights Sr. Analyst
DiDi Global —Buenos Aires, Buenos Aires
Engineering Technician
Allegro MicroSystems, LLC —Buenos Aires, Buenos Aires
- Tiempo completo
Production & Revenue Accounting Analyst
ExxonMobil —Capital Federal, Buenos Aires
Assistant Financial Controller
DataCamp —Capital Federal, Buenos Aires
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DualEntry - Lead Mobile
Silver.dev —Buenos Aires, Buenos Aires
- Tiempo completo
7d
Senior Accountant
DataCamp —Capital Federal, Buenos Aires
Postulación rápida
Sr. Accountant
Howard —Buenos Aires, Buenos Aires
- Tiempo completo
Postulación rápida
10d
Analyst, GSS Accounting Operations
Wyndham Hotels & Resorts —Buenos Aires, Buenos Aires
Senior Accountant (Remote)
Qventus —Capital Federal, Buenos Aires
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Coordinator, GSS FP&A
Wyndham Hotels & Resorts —Buenos Aires, Buenos Aires
Safety Specialist I
サイネオス・ヘルス —Buenos Aires, Buenos Aires
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Analyst, GSS FP&A
Wyndham Hotels & Resorts —Buenos Aires, Buenos Aires
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Wyndham Hotels & Resorts —Buenos Aires, Buenos Aires
Finance and Accounting Manager
Catch Creation, LLC —Buenos Aires, Buenos Aires
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Adverse Event Intake Coordinator

IQVIA -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo
Hace 5 horas

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Home-based | R1560782

Job overview:

The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our company's products. This position is responsible for receiving, reviewing, and processing incoming adverse event reports (AEs) from various sources, including healthcare professionals, consumers, and regulatory agencies. The ideal candidate is highly organized, detail oriented, and possesses strong communication and problem-solving skills.

Key Responsibilities:

Case Intake & Processing:
- Receive, review, and triage incoming AE reports from various sources.
- Creating, maintaining, and tracking case folders; filing, retrieving and distribution of case folders to operations team members.
- Perform ICSR surveillance on administrative topics and process including collection, reporting, follow-up processes.
- Accurately enter AE data into the company's safety database.
- Conduct initial case assessment and assign appropriate case status.
- Track and monitor the progress of AE investigations.
- Prepare case narratives and other relevant documentation.
- Assist with the preparation of safety reports for regulatory submissions.
Data Management & Quality Control:
- Assisting in maintenance of document control storage and relevant applications/systems as directed
- Providing key input to operations team on acquisition and/or upgrade of records management application/systems
- Ensure the accuracy and completeness of all AE data.
- Perform data entry and validation checks.
- Maintain accurate records and documentation.
- Support periodic audits and quality control checks on case processing
- activities.
Communication & Collaboration:
- Communicate effectively with internal and external stakeholders, including medical professionals, regulatory agencies, and other departments within the company.
- Collaborate with other team members to ensure timely and efficient case processing.
- Respond to inquiries and requests for information in a timely and professional manner.
Regulatory Compliance:
- Ensure compliance with all relevant regulatory requirements, including Good Pharmacovigilance Practices (GVP) and local regulations.
- Stay informed of any changes to relevant regulations and guidelines.
Process Improvement:
- Identify and implement process improvements to enhance the efficiency and accuracy of AE intake processes.
- Participate in team meetings and contribute to the development of best practices.

Qualifications:

Education: Bachelor's degree in a life science field (e.g., biology, pharmacy, nursing) or equivalent experience.
Fluent in local language and advanced English proficiency.
Experience: 1 year of experience in pharmacovigilance or a related field preferred.
Proficiency in Microsoft Office Suite (Word, Excel, Outlook)
Experience with electronic data capture (EDC) systems (Preferred)
Knowledge of medical terminology and coding systems (e.g., MedDRA) (Preferred)
Experience with regulatory submission (Preferred)

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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