IQVIA Hiring Regulatory Affairs Officer in Bangalore

Are you a skilled professional in Regulatory Affairs looking for an exciting opportunity in Bangalore? IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services, is currently hiring a Regulatory Affairs Officer for its Bangalore location.If you have the qualifications and are ready to advance your career with a top-tier company, this position could be the perfect fit for you.

Job Location and Type

Location: Bangalore, Karnataka
Job Type: Full-Time

Key Responsibilities

As a Regulatory Affairs Officer at IQVIA, Your main duties will include:

• Acts as a Regulatory Team Member on small, straightforward regulatory projects and/or gets involved in a small single service project, under the guidance of senior staff;
• Identifies project needs, tracks project timelines, implements client requests and manages day-to-day workload in collaboration with senior staff, as appropriate;
• Experienced in Regulatory knowledge in Chemistry, Manufacturing and Controls/ Lifecycle Maintenance/ Marketing Authorization Transfers/ Labeling/ Publishing as applicable;
• Prepares and/or reviews regulatory documentation in area of expertise, as appropriate;
• Actively participates in project teams with internal and external customers independently and communicates confidently in straightforward matters;
• Understands the Scope of Work, deliverables for any given project;
• May prepare slides and background material for small, straightforward business development meetings under senior guidance and presents in client  meetings by phone or in person;
• May prepare and deliver trainings, as appropriate;
• Performs other tasks or assignments, as delegated by Regulatory management;
• Responsible for making minor changes in systems and processes to solve problems where problems faced are not typically difficult or complex;

Qualifications

To qualify for the position of Regulatory Affairs Officer at IQVIA, candidates must meet the following criteria:

• Bachelor’s Degree Degree in Lifescience or related discipline Req Or
• Master’s Degree Degree in Lifescience or related discipline Req
• At least  2 years relevant experience
• Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate;
• Good, solid interpersonal communication (oral and written) and organisation skills;
• Ability to establish and maintain effective working relationships with coworkers, managers and clients;
• Strong software and computer skills, including Microsoft Office , publishing applications and tools, as applicable;
• Demonstrates self-motivation and enthusiasm;
• Ability to work on several projects, with direction from senior staff as appropriate;
• Ability to follow standard operating porcedures consistently; provides independent thought to assist in process improvements;
• Ability to make decisions on discrete tasks under senior supervision;
• Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education;
• Makes adjustments or recommended enhancements in systems and processes to solve problems or improve effectiveness of job area;
• Problems faced are general and may require understanding of broader set of issues, but typically are not complex;
•  Applicable certifications and licenses as required by country, state, and/or other regulatory bodies

How to Apply

Apply now through the link below. Ensure your application showcases your relevant experience and qualifications.

Apply Here

Tagged as: Good Clinical Practice (GCP), Pharmaceutical Jobs