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Associate Consultant, Regulatory Affairs (Medical Devices)

Singapore, Singapore Full time R1420252

Singapore, Singapore

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level

Build a rewarding career in life sciences consulting and forge your own path. Partner with collaborative teams and leaders across unique projects and geographies, delivering innovative solutions to the most complex healthcare problems along the way. Working at IQVIA means changing outcomes for patients one data set, product offering and innovative solution at a time.

As a Consultant at IQVIA, you'll have the opportunity to grow your career and explore opportunities in brand and integrated research solutions, go-to-market strategy, commercial excellence, real world data, financial investor consulting and more.

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Success Profile

What makes a Consultant at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.

  • ACHIEVER
  • ADAPTABLE
  • COMMUNICATOR
  • STRATEGIC
  • CRITICAL-THINKER
  • DETAIL-ORIENTED

What you can expect

Professional Development

Environments that advance your skillset

Highly Specialized

Work in distinctive areas of expertise

Growth Potential

Clear pathways to success

Collaboration

Teams that work together to achieve common goals

Innovative Projects

Projects that solve complex problems in new ways

Best-in-Class Training

Programs to help you build knowledge and gain skills

I joined IQVIA after graduating from university and am grateful for the fantastic opportunities I've been able to pursue over the last four years. I've had the chance to work with inspiring managers who have supported me with both professional and personal development.

Arthur

Consultant, Financial Institutions

I simultaneously work on a number of customer-commissioned projects in multiple therapeutic areas using various primary research methodologies. This variety is what makes my role so interesting. It allows me to learn from my colleagues and customers alike and helps me to understand how the work we do supports the improvement of patient care.

Julia

Senior Consultant, Brand and Integrated Research Solutions

IQVIA has given me the opportunity to gain a broad range of skills and experience across multiple disease areas and at different stages of the product lifecycle. This has supported my career development and accelerated my growth. If you enjoy learning new things and working on global projects, you will definitely enjoy working at IQVIA.

Kevin

Consultant, Brand and Integrated Research Solutions​

One of the things I like most about working at IQVIA is the supportive environment that helps you achieve your full potential.

Ana

Consultant, Financial Institutions

Working in healthcare consulting is inspiring! I am glad to be part of a close community that brings together diverse experiences and critical thinkers to help our customers move treatments forward that can change patients’ lives.

Jose

Principal, Consulting Services

Associate Consultant, Regulatory Affairs (Medical Devices)

Singapore, Singapore R1420252
Apply Now

Job Description

Responsibilities:

  • Assist the Head of Regulatory services in assuming primary or secondary regulatory responsibility for assigned projects by providing the project team with regulatory information, guidance, training, support and strategic planning based on applicable regulations issued by the regulatory agencies across JAPAC.

  • Deliver on regulatory projects in a timely and proactive manner.  Manage projects by coordinating with in-country regulatory team leads.

  • Identify and interpret regulations, guidelines, and other pertinent information issued by the applicable regulatory agencies and other regulatory organizations.

  • Review scientific data, publications, and related papers, as appropriate for various regulatory projects to ensure compliance with regulations. (Strategic guidance, dossiers preparation, submission activities & etc.)

  • Develop effective product registration strategies by performing critical review and gap analysis of product documentation.

  • Establish relationships with regulatory agencies, health bodies, internal and external stakeholders.

  • Ensure revenue is recognized by managing professional activities and internal stakeholders’ finances allocation.

  • Deliver training workshops and regulatory webinar to internal and external stakeholders.

  • Assist in identifying business opportunities for regulatory projects.

Requirements:

  • 3 - 5 yrs of regulatory affairs experience

  • Demonstrate comprehensive regulatory affairs expertise. aptitude for activities related to regulatory affairs and quality compliance for products market access and maintenance.

  • Familiarity with regulatory documents, general contents and the methods of filing and tracking.

  • Good interpersonal and negotiating skills, with an ability to identify and resolve issues efficiently and effectively.

  • Ability to read/synthesize technical materials and prepare clear/concise written documents.

  • Ability to juggle competing priorities to meet deadlines while maintaining high quality work.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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