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Regulatory Affairs Consultant

ClinChoice

Long Island NYMid
Sign in to applyVerified 1h ago
Location
Long Island NY
Work model
On-Site
Level
Mid
Posted
10d ago

About this role

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 an Regulatory Affairs Consultant Hybrid for 3 months Contract to join one of our clients.

Job Description

This position is directly responsible for supporting global market access including ensuring products dossiers address regulatory requirements (both existing and emerging).

Assemble (gather/create) all necessary technical and registration documentation in conformity with legal regulations of the marketing countries in order to meet local on counter dates.

• Coordinate and ensure maintenance of Brand/Market Registration Tracking databases in cooperation with affiliate, law firm and distributor counterparts, ensuring consistency and timely registrations and data integrity.

• Research, generate and distribute registration documentation; including formulas, specifications, Certificates of Free Sale, durability, claims substantiation, supporting declarations and artwork – according to specified local market regulations. Partner with seasoned mentor to provide appropriate support and follow-up with markets to secure registration and achieve market launch timelines. Maintain and update registration databases in order to ensure end-to-end registration compliance and consistency. Provide regular follow-up with market to ensure accuracy of data and compliance with expiry/re-registration timelines per market. Interface with trade associations and health authorities to secure brand/product and market specific Certificates of Free Sale. Coordinate additional data and information requests with R&D and Regulatory Compliance, obtaining efficacy reports to support product registration, package claims and durability reports. Liaise with brand GBSC and Marketing to track and obtain final product/shade names and codes. Perform research with brand and/or PDS to obtain all variant/kit/set/size artwork and country of origin information required to action and complete product registration on a sku and/or family level, depending on market requirements.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and

Listing verified 1h ago. Applications go through the company's official careers site.

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Regulatory Affairs Consultant at ClinChoice, Long Island NY | Yoinka