Skip Navigation

Senior Regulatory Affairs Associate - Labelling Specialist

, Brazil Date posted 10/23/2024 Job ID R0000020514

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.

In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Success Profile

Check out the top traits we're looking for and see if you have the right mix.

  • Detail-Oriented
  • Proactive
  • Problem-Solver
  • Results-Driven
  • Organized
  • Multi-Tasker
  • "When submitting major market applications, it’s key to ensure that the technical integrity of all data meets regulated requirement standards. Parexel makes this possible with a diverse team of seasoned professionals who care about getting important medicines to patients. This is Regulatory Operations at its best."

    Chris – Associate Director, Regulatory & Access
  • "In this role, I have had the unique opportunity to work with regulatory experts who are not only some of the most distinguished in their field, but are also some of the most compassionate people I know. I’ve been able to grow so much professionally by standing on the shoulders of giants!"

    Riley – Regulatory Affairs Consultant

Rewards

  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Management

    Strong management with depth of experience working for global health authorities.

Responsibilities

We are seeking a skilled and experienced Regulatory Labeling Specialist to join our team. This client-facing role requires expertise in general labeling processes, regulatory procedures, and advanced document editing skills. The ideal candidate will work closely with clients and internal teams to ensure accurate and compliant labeling for pharmaceutical products across various markets.

Key Responsibilities:

  • Apply comprehensive knowledge of labeling procedures and timelines, particularly for the Centralized Procedure in the EU.
  • Demonstrate a thorough understanding of the structure and authoring requirements for US Prescribing Information (USPI) and Canada Product Monographs.
  • Utilize advanced Microsoft Word editing skills, specifically for structured labeling documents.
  • Interact directly with clients, addressing their needs and queries related to labeling processes and requirements.
  • Ensure all labeling documents comply with regulatory standards and guidelines.
  • Collaborate with cross-functional teams to coordinate labeling activities and timelines.
  • Stay updated on regulatory changes and industry best practices in labeling.

Qualifications:

  • Bachelor's degree in Life Sciences, Pharmacy, or a related field (advanced degree preferred).
  • Minimum of 3-5 years of experience in regulatory affairs or labeling within the pharmaceutical industry.
  • In-depth knowledge of global regulatory labeling requirements, with a focus on EU, US, and Canadian markets.
  • Proficiency in advanced Microsoft Word features, particularly those related to structured labeling.
  • Excellent written and verbal communication skills in English.
  • Strong attention to detail and ability to manage multiple projects simultaneously.
  • Proven experience in client-facing roles within the pharmaceutical or healthcare industry.

Required Skills:

  • Expertise in regulatory labeling processes and timelines.
  • Proficiency in authoring and editing USPI and Canada Product Monographs. Advanced Microsoft Word skills, particularly in structured labeling techniques. Strong interpersonal and communication skills for effective client interactions. Ability to work independently and as part of a team in a fast-paced environment.

If you are passionate about regulatory affairs, have a keen eye for detail, and enjoy working directly with clients, we encourage you to apply for this exciting opportunity to contribute to our organization's success in the pharmaceutical labeling field.


#LI-REMOTE

Join our Talent Community

Welcome to the Parexel Talent Community! Sign up below and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.

Recently Viewed Jobs

You have not recently viewed any jobs

View all jobs

RECRUITMENT FRAUD ALERT

It has been brought to our attention that there has been fraudulent activity by scammers attempting to represent themselves as Parexel employees or recruiters. These individuals are attempting to reach potential job seekers through online chat interviews and sending false offer letters, representing Parexel without our consent. If you’re concerned that you’ve been contacted by an unauthorized Parexel recruiter or employee, please notify Jobs@Parexel.com. You may also report suspicious fraudulent activity to your local law enforcement agency or the FBI. Thank you.

@* *@