Freelance / Contractual Clinical Research Associate (experience in Dermatology) - Spain

TN Spain; Madrid; Presencial; EUR 30.000 - 60.000; Jornada completa

Descripción de la vacante

Una empresa innovadora busca un Asociado de Investigación Clínica Freelance con experiencia en dermatología. En este rol, serás responsable de monitorear estudios clínicos, asegurando que se realicen conforme a los procedimientos y regulaciones. Si te apasiona la dermatología y deseas contribuir a un entorno colaborativo donde tus aportes son valorados, esta es la oportunidad ideal para ti. Con un enfoque en la innovación y la excelencia, tendrás la oportunidad de trabajar con colegas talentosos y hacer una diferencia significativa en la investigación clínica.

Formación

• 3 años de experiencia en monitoreo clínico en la industria biotecnológica o farmacéutica.
• Conocimiento sólido de los estándares ICH/GCP y requisitos regulatorios.

Responsabilidades

• Realizar visitas de calificación, iniciación, monitoreo y cierre de sitios de investigación.
• Construir relaciones productivas con investigadores y personal del sitio.

Conocimientos

Monitoreo clínico

Conocimiento de ICH/GCP

Comunicación verbal y escrita en inglés

Resolución de problemas

Atención al detalle

Educación

B.Sc. en un campo relevante para la investigación clínica

Título en enfermería

Herramientas

Microsoft Office

Descripción del empleo

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Freelance / Contractual Clinical Research Associate (experience in Dermatology) - Spain, Madrid

Client: Indero

Location: Madrid, Spain

Job Category: Other

EU work permit required: Yes

Job Views: 2

Posted: 25.04.2025

Expiry Date: 09.06.2025

Job Description:

Freelance / Contractual, CRA with experience in Dermatology, Spain

The Contractual Clinical Research Associate (cCRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

This role will be perfect for you if:

• You are an experienced CRA with a demonstrated ability to work autonomously to meet quality standards and deadlines
• Focusing on dermatology and developing an expertise in this therapeutic area is interesting to you
• You enjoy working for a mid-sized CRO where your contributions are noticed and valued

RESPONSIBILITIES

The cCRA will:

• Conduct site qualification, initiation, monitoring, and close-out visits for research sites according to the monitoring plan, Indero and sponsor SOPs, ICH/CGP guidelines and applicable regulations
• Participate in investigators’ meetings
• Prepare site visit reports and follow-up letters to the investigator
• Build productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targets
• Perform source data verification, ensure on-site study drug storage, dispensing, and accountability, data collection, and regulatory document collection is adequate
• Employee may be assigned to other responsibilities that do not pertain to their former description, if they have the required experience, are qualified and/or have received adequate training

Our company:

The work environment

At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

Recruitment process: what to expect

• As part of the recruitment process for this position you will meet various team members at Indero
• The first interview will be conducted by Teams (30 minutes) and the second via video conference (1 hour)

About Indero

A Global Clinical Leader InDermatology!

Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.

Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale.

Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

Indero only accepts applicants who can legally work in Spain.

Education

• B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience

Experience

• 3 years of experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry
• At least 1 year of experience in dermatology

Knowledge and skills

• Good knowledge of ICH/GCP standards and applicable regulatory requirements
• Strong verbal and written communication skills in English
• Ability to prioritize different assignments and work under pressure while maintaining attention to detail and meeting timelines
• Excellent judgement and problem-solving skills
• Travel to research sites approximately 65% of the time
• Excellent knowledge of Microsoft Office (i.e., Word, Excel, PowerPoint)
• Experience in dermatology is an asset