Regulatory Affairs Associate

Regulatory Affairs Associate




Regulatory Affairs Associate

Detalles de la oferta

Buenos Aires, Buenos Aires

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.

- Full Time
- Level: Mid
- Travel: Yes

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


- 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.

We are in the process of recruiting a bi-lingual (English and Spanish) Regulatory Affairs Associate to work from our office in Buenos Aires. As a Regulatory Affairs Associate you will coordinate the regulatory workflow to obtain clinical trial approvals from regulatory authorities, provide regulatory consultancy to the team, and interface with the project team, the sponsor and regulatory authorities on strategic regulatory and technical matters for Argentina and other Latin American countries.

To be considered for this role, you must have experience working in a CRO in a regulatory role. Fluency in English is required as well as a university degree in health science or pharmacy.

Please submit English CV for consideration.


- CRO work experience in Regulatory submissions
- Education in health sciences or pharmacy
- Solid experience with computer systems
- Fluency in written and spoken English and Spanish

Fuente: Kitempleo




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