Regulatory Affairs Jobs at IQVIA
A rare chance has emerged for professionals in the life sciences sector to apply for regulatory affairs jobs at IQVIA. This opportunity is based in Thane, India, and offers a home-based work option. Qualified candidates are encouraged to explore this position and apply promptly.
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organisation creates intelligent connections to accelerate the development and commercialisation of innovative medical treatments, ultimately improving patient outcomes and population health worldwide. With a commitment to integrity, IQVIA maintains a zero-tolerance policy for candidate fraud and emphasises the importance of honesty in the hiring process.
Job Details:
- Company: IQVIA
- Job Title: Regulatory Affairs Officer 2
- Location: Thane, India | Home-based
- Job Type: Full-time
- Reference Number: R1557288
Job Overview:
Individual contributor who is fully proficient in applying subject matter knowledge for a professional discipline. Works under limited supervision.
Job Description:
This role involves acting as a Regulatory Team Leader on complex projects, preparing and reviewing regulatory documentation, and establishing relationships with customers. The individual will also act as a Subject Matter Expert in various regulatory areas and may provide guidance to junior colleagues. The position requires a strong understanding of the Research and Development process and the ability to adapt quickly to a rapidly changing environment.
Key Responsibilities
- Acts as a Regulatory Team Leader on more complex projects, which may include technical writing.
- Prepares and/or reviews regulatory documentation in area of expertise, as appropriate.
- Establishes relationships with many customers; may meet face to face without the rest of the team to discuss regulatory issues.
- Acts as an SME/expert in Regulatory knowledge in Chemistry, Manufacturing and Controls/Lifecycle Maintenance/Marketing Authorization Transfers/Labeling/Publishing as applicable.
- May give guidance to junior colleagues, including feedback on the quality of technical documents.
- May present to clients on complex regulatory processes at large full-service bid defence meetings.
- May prepare and deliver regulatory training to IQVIA small groups or individuals.
- Performs other tasks or assignments, as delegated by Regulatory management.
Eligibility Criteria:
• Bachelor’s Degree in Life Sciences or related discipline required.
• Master’s Degree in Life Sciences or related discipline preferred.
• At least 3-4 years of relevant experience.
• Good understanding of the Research and Development process, laws, and related guidelines.
• Possesses specific regulatory or technical expertise.
Required Skills:
• Strong interpersonal communication (oral and written) and organisational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Strong software and computer skills, including Microsoft Office and publishing applications.
• Ability to follow standard operating procedures consistently and provide independent thought for process improvements.
Why Join IQVIA:
Working at IQVIA offers professionals the chance to contribute to meaningful projects in the life sciences sector while enjoying the flexibility of work-from-home options. The organisation fosters a culture of integrity and innovation, making it an excellent choice for those seeking to advance their careers in regulatory affairs.
