20 publicaciones de empleo destacadas de clinical research en barcelona, ct (¡Están contratando!)

Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Investigación
3d
Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)
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Alira Health —Barcelona, Barcelona provincia
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Lead Data Scientist - BCN/MAD/Munich
ailylabs —Barcelona, Barcelona provincia
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- Oficina
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Risk Surveillance Lead
Novartis —Barcelona, Barcelona provincia
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SSU CRA II Barcelona. Sponsor dedicated
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Grado
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Senior Project Manager / Associate Project Management Director
Optimapharm d.o.o. —Barcelona, Barcelona provincia
- De 80.000 € a 100.000 € al año
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Máster
13d
Study Director Team Lead
Novartis —Barcelona, Barcelona provincia
- De 74.200 € a 137.800 € al año
- Jornada completa
- Investigación
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9d
Principal, Health Economics, Health Technology Assessment
IQVIA —Barcelona, Barcelona provincia
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- Trabajo híbrido
- Microsoft Excel
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- Inteligencia artificial
VAC_64_2026 - SENIOR LEGAL OFFICER
Institut de Recerca contra la Leucèmia Josep Carreras —Badalona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Hospital
- Inglés
22h
Project Manager
Barcelona Institute for Global Health (ISGlobal) —Barcelona, Barcelona provincia
- Media jornada
- Español
- Doctorado
- Inglés
10d
Associate Medical Director- Neurology
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Amics del VHIR - Institutional call for the incorporation of Early-stage (R1) researchers
VHIR —Barcelona, Barcelona provincia
- De 19.563 € a 25.079 € al año
- Microsoft Excel
- Doctorado
- Hospital
7d
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
RESOLUCIONES DE CONVOCATORIAS 2025
IGTP —Badalona, Barcelona provincia
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- Enfermería
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Data Science Consultant, Discovery & Translational Science
Clarivate —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
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Medical Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 69.000 € a 128.100 € al año
- Jornada completa
- Enfermería
- Inglés
- Inteligencia artificial
1d
Senior Director, Drug Development
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
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- Investigación
- Teletrabajo opcional

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Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona

サイネオス・ヘルス
Barcelona, Barcelona provincia

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Detalles del empleo

Hace 3 días

Cualificaciones

Investigación clínica
Investigación

Descripción completa del empleo

Updated: Today
Location: Barcelona, Spain
Job ID: 25111321

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Description

Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona

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

Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions.
Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines
Creates and assists with maintenance of project files, handles project correspondence
Participates in file audits
Prepares and maintains site manuals, reference tools and other documents
Maintains, updates, and inputs clinical tracking information into databases
Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client
Manages shared mailbox, processes site requests and routes correspondence appropriately
Coordinates the ordering, packaging, shipping and tracking of site supplies and materials
Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items
Routinely anticipates, identifies and resolves potential issues and implements corrective actions, seeking guidance as needed to resolve more complex issues
Maintains overall awareness in the field of clinical research, as well as assigned areas, by completing all necessary and assigned training.
May provide training or mentorship to more junior level Clinical Operations Specialists (COS).

Qualifications

Associates degree preferred or equivalent
Solid clinical Study Start-Up experience
Regulatory and/or CTA background and submissions experience will be highly preferred
Experience in clinical research/pharma/biotech or related field considered In lieu of degree
Good knowledge of medical terminology, clinical data, and ICH/GCP preferred
Ability to successfully prioritize and work on multiple tasks
Strong attention to detail, accuracy and organizational skills
Excellent communication, presentation, and interpersonal skills
Ability to embrace new technologies
Minimal travel up to 10% may be required

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

Roles within Clinical Operations are responsible for ensuring safe and effective operations of clinical research studies. Responsible for safeguarding the wellbeing of research subjects in a medical capacity. Reviews study protocols, plans and executes procedures in alignment with protocols and regulatory, health, and safety standards, raising or escalating study issues. Recruits and coordinates communication with clinical trial volunteers and patients, and follows applicable regulations globally and by region. Collaborates with cross-functional teams to develop study materials, monitor trial progress, and address any issues that arise during the study. Impact and Contribution Individual contributors who provide organizational related support or service (administrative or clerical), as well as roles operating in support of daily business activities (e.g., technical, production, or craft levels). The majority of time is spent in the delivery of support services or activities, typically under supervision. Roles do not typically require advanced education or training. Established and experienced support individual contributor. Work consists of tasks that are typically routine, with some deviation from standard practice. Requires broad knowledge of operational systems and practices typically gained through extensive experience and/or education.

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clinical research empleos en barcelona, ct

Sponsor Dedicated Sr. SSU CTA - Hybrid Barcelona

Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)

Associate Consultant

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VAC_64_2026 - SENIOR LEGAL OFFICER

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Amics del VHIR - Institutional call for the incorporation of Early-stage (R1) researchers

Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

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Medical Safety Lead - CRM

Senior Director, Drug Development

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