Regulatory Affairs Associate Consultant

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds.

ClinChoice is searching for a Regulatory Affairs Associate Consultant to join one of our clients.

**Main Job Tasks and Responsibilities**:

- Preparation, compilation, and coordination of high-quality regulatory submissions for new product launches, product updates, and throughout the product lifecycle.
- Support coordination of label change initiation, label reviews and changes in accordance with regional /country review system and procedure.
- Provide regulatory input, review and approval related to change control.
- Support product portfolio through execution of legal document activities as required.
- Preparation and compilation of regulatory documentation for submission
- Develop and manage regulatory action item tables for country-specific requirements.
- Work with client regulatory managers to develop project implementation plans and manage workload planning to ensure on-time completion of projects and tasks.
- Support client regulatory managers in their registration procedure.
- Provision of weekly updates (at a minimum) to relevant client regulatory managers
- Ensure regulatory standards and timelines are met.
- Plan and track the status of ongoing regulatory projects.
- Regulatory action item tables for country-specific requirements and importation/ exportation needs for change in legal entity.
- Ensuring documents for health authority are submission ready.
- Supporting coordination of label change initiation, label reviews and changes in accordance with regional /country review system and procedure.
- Regulatory input, review and approval related to Change Control.

**Education and Experience**:

- 5+ years of relevant experience with BSc in Pharmacy or related health sciences.
- Must have knowledge of regulations for Cosmetics in Andean Markets (Columbia, Ecudor, Peru, etc).
- Language: English is required.
- Portuguese is desirable.
- Strong working knowledge of Microsoft Word, Excel, Power Point
- Good communication and follow-up skills with country regulatory liaisons for clear understanding of country specific needs for registrations, license updates and import/export requirements.

**The Application Process**:
**Who will you be working for?**

**About ClinChoice**:
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

**Our Company Ethos**:
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

**#LI-TT1**

**ClinChoice is an Equal Opportunity Employer / Committed to Diversity