
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Regulatory Affairs Associate (Labeling Variations coordination) is responsible for managing labeling ensuring that biological product labels, artwork, translation and packaging components comply with the regulatory requirements of each Local country. The role supports marketing authorization submissions, lifecycle management, and post approval variations requiring labeling updates.
Key Accountabilities:
A. Labeling & Artwork Management
Prepare, review, and update product labeling according to requirements from Health authorities.
Ensure localized labeling content (language, warnings, dosage, contraindications) complies with each country’s standards.
Coordinate artwork development and version control with internal teams and external vendors.
B. Regulatory Submissions
Support Marketing Authorization Applications (MAAs), renewals, and variations that involve labeling changes.
Prepare labeling sections of the dossier per local format (CTD/eCTD with country‑specific annexes).
C. Cross‑Functional Collaboration
Work closely with RA, QA, supply chain, artwork teams, and local affiliates to ensure labeling accuracy and timely updates.
Act as liaison between global teams and local representatives.
Business Development
Begin networking within the industry (i.e. maintain contacts and relationships with clients once engagements are complete)
Communicates potential new business led to PC management and account managers.
Parexel-related Activities
Meets established metrics as specified in scorecard on an annual basis
Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, training compliance, project deliverable archiving, participation in internal initiatives/projects.
Defines self-development activities with the support of management in order to keep current within the industry.
Skills:
Client-focused approach to work.
Results orientation.
Teamwork and collaboration skills.
Consulting skills.
Excellent interpersonal and intercultural communication skills, both written and verbal.
Critical thinking and problem-solving skills.
Proficiency in local language and extensive working knowledge of the English language.
Knowledge and Experience:
Initial years of experience in an industry-related environment.
Education:
Minimum of a bachelor’s degree in a Scientific or Technical Discipline.

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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