Senior Regulatory Affairs Coordinator at IQVIA

New Cairo City, Cairo Governorate, Egypt

IQVIA Logo
Not SpecifiedCompensation
Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Healthcare, Life SciencesIndustries

Requirements

  • Bachelor’s degree in Pharmaceutical Science or related field
  • Minimum 1 year of experience in Regulatory Affairs (Cosmetics and Nutritional Products) within Egypt or GCC; experience with medical devices is a plus
  • Strong knowledge of good documentation practices and proficiency in HA systems and Microsoft tools
  • Excellent organizational, communication, and problem-solving skills
  • Fluency in local language and good command of English
  • Ability to manage multiple priorities with attention to detail

Responsibilities

  • Prepare, review, and organize regulatory documentation in line with IQVIA and health authority standards
  • Support timely submissions through Health Authority systems and maintain accurate records
  • Act as a liaison between clients and regulatory bodies, ensuring clear and effective communication
  • Identify opportunities for process improvement and contribute to best practices
  • Uphold quality and safety standards across all deliverables

Skills

Key technologies and capabilities for this role

Regulatory AffairsRegulatory DocumentationHealth Authority SystemsGood Documentation PracticesMicrosoft OfficeRegulatory SubmissionsCosmetics RegulationNutritional Products RegulationMedical Devices Regulation

Questions & Answers

Common questions about this position

What qualifications are required for the Senior Regulatory Affairs Coordinator role?

A Bachelor’s degree in Pharmaceutical Science or related field is required, along with a minimum of 1 year of experience in Regulatory Affairs for Cosmetics and Nutritional Products in Egypt or GCC. Experience with medical devices is a plus, plus strong knowledge of good documentation practices, proficiency in HA systems and Microsoft tools, and fluency in local language with good English command.

What are the key responsibilities of this position?

Responsibilities include preparing and reviewing regulatory documentation, supporting submissions through Health Authority systems, acting as a liaison between clients and regulatory bodies, identifying process improvements, and upholding quality standards.

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 does IQVIA offer in terms of career growth and company culture?

IQVIA offers continuous learning, career growth, and the chance to be part of a global team advancing healthcare through science and technology.

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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