Remote Global Regulatory Affairs Lead

IQVIA; Dubai; On-site; USD 19,000 - 30,000; Full time

Job summary

An established industry player is seeking a Regulatory Affairs Specialist to oversee regulatory activities for pharmaceutical products. In this role, you will manage submissions, ensure compliance with local regulations, and act as a subject matter expert. You'll collaborate with global pharmaceutical clients, preparing product labeling and managing multiple products. This position offers the chance to work in a dynamic environment that values innovation and teamwork, making a significant impact on public health. If you have a passion for regulatory affairs and a desire to contribute to a healthier world, this is the opportunity for you.

Qualifications

• 8-10 years of relevant experience in regulatory affairs.
• Masters in Life Sciences or related field required.

Responsibilities

• Manage local regulatory submissions and approvals.
• Act as a subject matter expert in regulatory processes.
• Provide guidance and training to junior colleagues.

Skills

Regulatory Compliance

Interpersonal Communication

Project Budget Management

Technical Document Quality Assessment

Fluent in English

Fluent in Arabic

Education

Masters Degree in Life Sciences

Job description

An established industry player is seeking a Regulatory Affairs Specialist to oversee regulatory activities for pharmaceutical products. In this role, you will manage submissions, ensure compliance with local regulations, and act as a subject matter expert. You'll collaborate with global pharmaceutical clients, preparing product labeling and managing multiple products. This position offers the chance to work in a dynamic environment that values innovation and teamwork, making a significant impact on public health. If you have a passion for regulatory affairs and a desire to contribute to a healthier world, this is the opportunity for you.