Adverse Event Intake Specialist at IQVIA

Beirut, Beirut Governorate, Lebanon

Apply Now

Not SpecifiedCompensation

Entry Level & New Grad, Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Healthcare, Life SciencesIndustries

Requirements

Bachelor’s degree in scientific, healthcare, or life sciences discipline
Fluency in English, Arabic, and French (minimum C1 level)
Up to 3 years of relevant experience (or equivalent education/training)
Strong knowledge of medical terminology and safety databases
Familiarity with global clinical research regulations
Proficiency in Microsoft Office and web-based applications
Excellent attention to detail, organizational skills, and time management
Strong communication skills and ability to work independently or in a team
Flexible, self-motivated, and eager to learn across safety service lines

Responsibilities

Prioritize and complete all assigned training on time
Review, assess, and process safety data according to regulations, SOPs, and project requirements
Perform pharmacovigilance activities including: collecting and tracking adverse events (AEs) and endpoint information; determining initial/update status of events; database entry, coding of AEs and products, and writing narratives; conducting literature searches and related activities
Maintain accurate case records and ensure compliance with project timelines
Meet quality, productivity, and delivery standards consistently
Identify and escalate quality issues promptly
Collaborate with cross-functional teams (clinical, data management, project management) and healthcare professionals to resolve project-related issues
Communicate effectively with clients regarding case processing details when required
Attend project meetings and provide feedback on challenges and successes
Mentor new team members and share best practices
Contribute to departmental initiatives and process improvements
Demonstrate problem-solving skills and adaptability to changing demands
Complete all mandatory training and maintain accurate documentation
Support medical review of non-serious adverse events (AEs) and adverse drug reactions (ADRs) when required
Ensure completeness and accuracy of data according to regulations and guidelines
Maintain flexibility to operate in shifts and manage multiple priorities under strict deadlines

Skills

Pharmacovigilance

Adverse Event Processing

Data Coding

Narrative Writing

Literature Search

Regulatory Compliance

SOPs

Database Entry

Case Management

Quality Control

Cross-functional Collaboration

Problem-solving

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

Land your dream remote job 3x faster with AI

Try Jobo Free