Global Regulatory Affairs Manager at IQVIA

New Cairo City, Cairo Governorate, Egypt

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, Healthcare, PharmaceuticalsIndustries

Requirements

Degree in Pharmacy or Life Sciences
Experience in regulatory affairs across international markets
Strong communication and collaboration skills
Proficiency in regulatory systems such as Veeva RIM
A proactive, solution-oriented mindset

Responsibilities

Develop and implement regulatory strategies for assigned products in partnership with global teams and local affiliates
Manage submissions, approvals, and lifecycle activities to meet timelines and regulatory requirements
Act as the key liaison between global regulatory teams and affiliates, ensuring alignment on priorities and documentation
Monitor regulatory changes and provide strategic guidance to internal stakeholders
Support health authority interactions, including briefing documents and response planning

Skills

Key technologies and capabilities for this role

Regulatory AffairsVeeva RIMRegulatory SubmissionsHealth Authority InteractionsRegulatory StrategyInternational MarketsCompliance

Questions & Answers

Common questions about this position

What qualifications are required for the Global Regulatory Affairs Manager role?

A degree in Pharmacy or Life Sciences is required, along with experience in regulatory affairs across international markets, strong communication and collaboration skills, proficiency in regulatory systems such as Veeva RIM, and a proactive, solution-oriented mindset.

What does the company culture at IQVIA look like?

IQVIA thrives on innovation, collaboration, and a shared mission to advance healthcare worldwide, where your potential has no limits and you can make an impact that matters.

Is this a remote position or does it require office work?

This information is not specified in the job description.

What is the salary or compensation for this role?

This information is not specified in the job description.

What experience makes a strong candidate for this position?

Candidates with a degree in Pharmacy or Life Sciences, experience in regulatory affairs across international markets, proficiency in Veeva RIM, and strong collaboration skills will stand out, especially those with a proactive mindset.

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.

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