20 publicaciones de empleo destacadas de clinical development en barcelona barcelona provincia (¡Están contratando!)

Senior Clinical Research Associate
Alira Health —Barcelona, Barcelona provincia
- De 55.000 € a 65.000 € al año
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Medical Science Liaison - Vaccines
CSL Seqirus —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Principal Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Investigación
- Máster
- Teletrabajo opcional
Clinical Research Associate
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
Clinical Research Monitor (Rheumatology Research Group)
VHIR —Barcelona, Barcelona provincia
- De 24.000 € a 27.000 € al año
- Jornada completa
- Microsoft Word
- Hospital
- Procesamiento de textos
12d
Clinical Global Development Scientist Director, Late Respiratory & Immunology
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Inglés
10h
GLOBAL CLINICAL DEVELOPMENT PHYSICIAN
Almirall —Sant Feliu de Llobregat, Barcelona provincia
- Jornada completa
- Inglés
- Microsoft Office
- Liderazgo
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Senior Clinical Research Associate 1 - Sponsor dedicated
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Investigación
- Teletrabajo opcional
Clinical Pricing & Payments Senior Associate _ Pricing
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
5d
Clinical Researcher–Physician Specialist in Allergy (Allergy Research Group)
VHIR —Barcelona, Barcelona provincia
- 20.000 € al año
- Media jornada
- Español
- Doctorado
- Hospital
8d
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- SQL
- Grado
7d
Bioinformatics Technician (Nephrology and Transplantation Research Group)
VHIR —Barcelona, Barcelona provincia
- De 23.393,80 € a 36.794,72 € al año
- Jornada completa
- Hospital
- Máster
- Grado
12d
Associate Principal - Mixed Methods Research: Patient Experience - Home-based/Hybrid
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Investigación
Associate Clinical Programmer - Clinical Data Operations
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- Inglés
- Investigación
5d
MEDICAL DOCTOR - TALENT COMMUNITY
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Investigación
- Cuidados al paciente
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Teletrabajo
- Doctorado
- Inglés
- Investigación
Clinical Research Associate 2 - CFSP
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Senior Scientist (Study Director) in the Small Molecule Bioanalysis department
Anapharm Bioanalytics —Barcelona, Barcelona provincia
- Español
- Doctorado
- Inglés

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Senior Clinical Research Associate

Alira Health -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa
De 55.000 € a 65.000 € al año

Cualificaciones

Investigación clínica
Servicio al cliente
Inglés
Investigación
Grado
Optimización de la conversión
Farmacia
Liderazgo

Descripción completa del empleo

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Sr CRA Spain

Job Description

ROLE

The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. The Sr CRA works closely with US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of Clinical Monitoring, CRAs, and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.

Salary range: € 55.000 - € 65.000

KEY RESPONSABILITIES

Provides guidance, oversight, and feedback to the CRA team to ensure adherence to project scope, SOPs, timelines, and budget requirements.
Reviews monitoring visit reports, conducts co-monitoring and evaluation visits as needed.
Ensures appropriate and timely investigator site visits.
Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues.
Assists in development of study-specific Monitoring Plans and training presentations as required.
Assists in set up/collection of site specific ethics documents and site contract negotiation as required.
Provides monthly billing information to finance team as required.
For monitoring stand-alone projects, manages study budget and acts as referent for the sponsor.
Performs qualification, initiation, interim, and close-out visits both remotely and onsite, ensuring proper documentation of monitoring visits.
Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
Ensures integrity of CRF data through meticulous and thorough source document review and verification.
Performs quality control and verification of documents collected at sites for eTMF/TMF.
Conducts investigational product accountability.
Reviews site regulatory binder for required documents.
Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.
Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company/Sponsor SOPs.
Participates in internal, client/sponsor, scientific, and other meetings as required.
Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.
Works closely with in-house CRAs/CTC and data management to resolve queries on discrepant data.
Proactively identifies site issues and develops problem-solving strategies for sites.
Conducts audit preparation at study sites as needed.
Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.
Participates in internal, client/sponsor, scientific, and other meetings as required.
Assists in CRA new hire training and onboarding.
Performs CRA mentoring.
Collaborates with development and maintenance of Clinical Trial Management System (CTMS).
Manages and resolves conflicting priorities to deliver on commitments.
Performs additional duties as assigned.

DESIRED QUALIFICATION & EXPERIENCE

US: BS/BA from an undergraduate program (life sciences or related discipline preferred)
US: 3 years of experience in the pharmaceutical / biotechnology / CRO industry, 2 year of clinical monitoring experience with 1 year of management experience
EU: Minimum 2 years of clinical monitoring experience in the pharmaceutical / biotechnology / CRO industry and ability to autonomously manage monitoring activities

TECHNICAL COMPETENCES & SOFT SKILLS

Quality focused; Proven ability to be careful, thorough, and detail-oriented
Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment
Able to manage priorities, organize time and solve problems
Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills
Ability to travel
Ability to manage stress
Professional, trustworthy and disciplined
Ability to problem-solve unstructured or ambiguous challenges
US: Strong command of English, both written and verbal
EU: Strong command of Local language, both written and verbal, in the country where monitoring activities are performed
Excellent communication and interpersonal skills with customer service orientation
Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture
Self-starter who thrives in a collaborative, yet less structured team environment
Knowledge of clinical research, ICH GCP and local regulations
Knowledge of Regulatory and Ethical requirements
Ability to establish and maintain positive relationships with Sponsor, Site and Project Team members
EU: Graduation in a scientific health field.
EU: Adequate English

Languages

English

Education

Bachelor of Science (BS): Biology, Bachelor of Science (BS): Biotechnology, Bachelor of Science (BS): Life Sciences, Bachelor of Science (BS): Pharmacy

Contract Type

Regular

Salary Range

The final offer will be determined within the applicable location-specific range and will depend on the candidate’s confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.

€ 55.000 - 65.000

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Refina tu búsqueda

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