Freelance Regulatory Affairs Portugal 0.3-0.4 FTE

Location:

Leira, Portuguese areas, Portugal

Salary:

Negotiable

Type:

Contract

Start Date: 

ASAP

Contract Period: 

6 months

Main Industry:

Search Health, Nursing & Social Services Jobs

Other Industries & Skills: 

Chemistry, Physics, Life Sciences

Advertiser:

NonStop Consulting

Job ID:

130725226

Posted On: 

27 June 2024

We are seeking several senior Regulatory Affairs professionals for a part-time (0.3 FTE – 0.4 FTE) freelance position in Portugal with our client, a leading company in the pharmaceutical industry. In this role, you will have the opportunity to work on the review and validation of promotional and non-promotional materials, as well as their regulatory submission. With over 1,000 clients and 250 senior experts, our client offers a collaborative work environment where you can develop your expertise from strategy to implementation.

They are looking for 4 people and candidates can be anywhere in Portugal and the company is flexible regarding the fee, they want the person to start as soon as possible.

Benefits:

– Work freelance with a flexible schedule that allows you to better manage your time.

– Collaborate on innovative projects with start-ups in the pharmaceutical sector.

– Join a global team with strategic partners around the world.

Your mission:

1) Operational support for review, validation and regulatory submission of promotional material in accordance with local requirements and approved texts:

– volume: around 150 to 200 materials by 2024.

2) Operational support for compliance of local events (congress, board of directors, staff…) with local regulations:

– The documents will be provided by our client translated into the local language of the client’s corporate material.

– Only regulatory validation and review of the linguistic consistency of the translation (medical validation is carried out by the company)

– One Version 1 and one Version 2/Final Version

– Email circuit (without workflow tool) and exchanges with the client project manager.

– Local presentation to Authorities if required locally

– Approximately between 150 and 200 materials by 2024

Requirements:

– Previous experience in regulatory review of pharmaceutical materials.

– Knowledge of local regulations in Portugal

– Ability to work autonomously and in collaboration with multidisciplinary teams.

-High English level

Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.

About NonStop: We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We’re passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting (nonstopconsulting), for more information, to browse all our roles, or to let us know how we can help you.

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