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

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs
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Chiesi Farmaceutici —Barcelona, Barcelona provincia
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Global Development Senior Medical Director, Hematology Oncology
AstraZeneca —Barcelona, Barcelona provincia
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Diagnóstic Grifols SA —Parets del Vallès, Barcelona provincia
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Novartis —Barcelona, Barcelona provincia
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- Jornada completa
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dsm-firmenich —Barcelona, Barcelona provincia
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Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

サイネオス・ヘルス
Barcelona, Barcelona provincia

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Detalles del empleo

Hace 9 días

Descripción completa del empleo

Updated: Yesterday
Location: Barcelona, Spain
Job ID: 25110718

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Description

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

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

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

Position Objective

Provide support for the end-to-end management of Early Access Programs, including Compassionate Use and Post-Trial Access programs, ensuring compliance with internal procedures, applicable regulatory requirements, and effective cross-functional coordination among all stakeholders involved.

Key Responsibilities

Program Operations Management

Coordinate the operational process for early access requests from receipt through to closure.
Manage and maintain tracking systems, databases, and case monitoring tools, ensuring all information remains accurate and up to date.
Monitor timelines, milestones, and required approvals for each request.
Ensure proper document management and maintenance of all case-related records.
Support the coordination of medication supply for active programs.

Cross-Functional Coordination

Serve as the primary point of contact for operational inquiries related to early access programs.
Coordinate activities across Medical Affairs, Pharmacovigilance, Supply Chain, Legal, and other relevant departments.
Facilitate communication with healthcare professionals and participating sites regarding operational aspects of the programs.

Regulatory Compliance and Quality

Ensure all activities are conducted in accordance with applicable regulations, internal procedures, and company quality standards.
Maintain complete, accurate, and audit-ready records of all activities performed.
Support the preparation of audits and inspections by providing the required documentation.

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

Experience managing compassionate use programs

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of regulatory affairs empleos en barcelona barcelona provincia

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

Local Quality Assurance Manager (GDP) Iberia

Global Quality Manager (m/f/x) - EU-based

Research Editor, Risk & Compliance Data, Arabic/French

Manager Risk Management

Intern SHE Adhesives

R&D Program Manager

Project Manager 1

Senior Manager Corporate Compliance - EMEA

Clinical Marketing

MEDICAL WRITING SENIOR MANAGER

Brand Manager Rare Diseases

Global Development Senior Medical Director, Hematology Oncology

Omnichannel Trade Lead

Director, Digital Platforms & Experience

CRM & Field Force Enablement Product Owner

QA PRODUCT RELEASE SECTION MANAGER

Sales Head Immunology

Senior Digital Architect - Product Domain

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