19 publicaciones de empleo destacadas en regulatory affairs (¡Están contratando!)

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Regulatory Associate - AdPromo
サイネオス・ヘルス —Tlalnepantla, Méx.
- Contratos
8d
Litigation Counsel
DiDi Global —Cuauhtémoc, CDMX
- Inglés
Site Activation Specialist - Futures Roles (Mexico)
サイネオス・ヘルス —Tlalnepantla, Méx.
- Hospital
- Contratos
Customs Analyst
Diageo —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Excel
- ERP systems
- Análisis de datos
1d
Business Compliance Manager
Revolut —Ciudad de México, CDMX
- Administración de personal
- Gestión de venta al por menor
- Experiencia en operaciones bancarias
Sr Spec, IT-Global Serialization
Baxter —Guadalajara, Jal.
- Inglés
- Licenciatura
- Negociación
- Vacaciones adicionales o permisos con goce de sueldo
6d
Commercial Director
Bracco —Tlalpan, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Excel
- Administración de personal
Head of Trade LATAM & Pharma Mexico
Sanofi —Ciudad de México, CDMX
- Administración de personal
- Experiencia en ventas
- Hospital
Office Manager
TRALICOM —Colonia Polanco, CDMX
- $15,000 a $22,000 por mes
- Tiempo completo
- Bilingüe
- Español
- Microsoft Excel
Postulación rápida
11d
Sr. Risk Management Engineer
Fresenius Medical Care —Reynosa, Tamps.
- Bilingüe
- Administración de personal
- Inglés
Trade Business Manager (Out-Licensing), Mexico
Viatris —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Mercadotecnia
- Inglés
Product Manager (Mexico City)
BeiGene —City, Hgo.
- Tiempo completo
- Administración de personal
- Doctorado
- Experiencia en ventas
Office Manager
FENIXFARMA —Colonia Polanco, CDMX
- $15,000 a $22,000 por mes
- Tiempo completo
- Español
- Microsoft Excel
- Mantenimiento
Postulación rápida
11d
Medical Director (Endocrinology)
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Disponible para viajar
- Seguro dental
- Seguro de la vista
Sr Associate - Consumer Digital Ecosystem
Eli Lilly —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Disponible para viajar
7d
Senior Clinical Data Engineer (LATAM)
Precision Medicine Group —Desde casa
- Home Office (Desde casa)
- Administración de personal
- Inglés
- SQL
Technical Services Analyst
Kemin —Zapopan, Jal.
- Tiempo completo
- Ingeniería
- Inglés
- Licenciatura
Diseñador Gráfico Freelance
Innova Talent - Soluciones Humanas —Zapopan, Jal.
- $500 por día
- Por temporada
- Licenciatura
- Trabajo desde casa
Postulación rápida
Senior Clinical Data Engineer (LATAM)
Precision for Medicine —Desde casa
- Home Office (Desde casa)
- Administración de personal
- Inglés
- SQL
Postulación rápida

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Regulatory Associate - AdPromo

サイネオス・ヘルス
Tlalnepantla, Méx.

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Información del empleo

Hace 8 días

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Descripción completa del empleo

Updated: Yesterday
Location: Tlalnepantla, MEX, Mexico
Job ID: 25108925-OTHLOC-7302-2DR

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Description

Regulatory Associate - AdPromo

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Build and institutionalize regulatory project management frameworks, tools, and best practices to enhance GRA-AP capability and effectiveness.

Provide oversight of GRA-AP projects and portfolios, ensuring alignment with objectives and timelines.
Coordinate and facilitate communication among regulatory affairs, project teams, stakeholders, and external partners to support project execution.
Track project progress, materials, and deliverables, proactively identifying and resolving issues to maintain project momentum.
Lead and participate in regulatory project meetings, including documenting minutes, updating project portals, and communicating outcomes to stakeholders.
Perform administrative functions to support project teams and department operations.
Assume additional duties as assigned to ensure regulatory project and portfolio success.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

Under supervision, supports regulatory agency submissions, regulatory research, and product development. Responsibilities typically include the creation of submission documents to support investigational new drug applications (INDs), new drug applications or new marketing applications (NDAs/MAAs), drug master files (DMFs), variations, renewals, marketing authorisation transfers (MATs) and other lifecycle maintenance activities.

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regulatory affairs empleos

Regulatory Associate - AdPromo

Litigation Counsel

Site Activation Specialist - Futures Roles (Mexico)

Customs Analyst

Business Compliance Manager

Sr Spec, IT-Global Serialization

Commercial Director

Head of Trade LATAM & Pharma Mexico

Office Manager

Sr. Risk Management Engineer

Trade Business Manager (Out-Licensing), Mexico

Product Manager (Mexico City)

Office Manager

Medical Director (Endocrinology)

Sr Associate - Consumer Digital Ecosystem

Senior Clinical Data Engineer (LATAM)

Technical Services Analyst

Diseñador Gráfico Freelance

Senior Clinical Data Engineer (LATAM)

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