Clinical Scientist

TN Spain; Sant Cugat del Vallès; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

Una empresa innovadora busca un Científico Clínico para unirse a su equipo de Desarrollo Clínico. Este rol es esencial para desarrollar estrategias científicas para nuevas indicaciones y evaluar la literatura científica. El candidato ideal tendrá una licenciatura en Ciencias de la Salud y experiencia en ensayos clínicos. Se valorarán habilidades analíticas y la capacidad de trabajar en equipos multidisciplinarios. La empresa ofrece un entorno de trabajo colaborativo y oportunidades de desarrollo profesional, haciendo de esta una oportunidad brillante para avanzar en su carrera. ¡No pierdas la oportunidad de unirte a un equipo que valora la diversidad y el crecimiento!

Formación

• 2+ años de experiencia como Científico de Ensayos Clínicos o 5+ años como Líder de Programa Clínico.
• Experiencia significativa en producción de documentos clínicos y estrategia de ensayos clínicos.

Responsabilidades

• Diseñar y desarrollar protocolos de estudio y colaborar con equipos de Biostatística y Operaciones Clínicas.
• Apoyar al departamento regulatorio en reuniones con autoridades sanitarias y revisar documentos de estudio.

Conocimientos

Habilidades analíticas

Trabajo en equipo

Pensamiento estratégico

Fluidez en español e inglés

Educación

Licenciatura en Ciencias de la Salud

Descripción del empleo

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Client:

Grifols

Location:

Job Category:

Other

EU work permit required:

Yes

Job Views:

2

Posted:

24.04.2025

Expiry Date:

08.06.2025

Job Description:

We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

Instituto Grifols is seeking a Clinical Scientist for our Clinical Development team.

This role’s mission is to contribute to developing scientific strategies for new indications, evaluate scientific literature, and interpret data for regulatory documents. It supports MDs with clinical inquiries, ongoing trials, risk evaluation, safety narratives, and Advisory Boards, ensuring smooth regulatory and trial processes.

What your responsibilities will be:

• Participate in the design and development of study protocols/protocol amendments, supporting the lead physician in creating overall clinical programs for new therapeutic indications.
• Collaborate with Biostatistics, Clinical Operations, Pharmacology, and Pharmacovigilance teams to oversee ongoing programs with several clinical studies and to address various indications in development for business considerations.
• Synthesize literature and competitive intelligence to inform study designs and results within the assigned therapeutic area.
• Contribute to (and/or review) specific study documents managed or owned by clinical/regulatory groups, such as Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, clinical section reviews of BLAs, SAE narrative construction, etc.
• Support the Regulatory department in preparing for Health Authority meetings (e.g., pre-IND meetings, and briefing meeting requests & packages).
• Support Clinical Operations throughout trial execution, providing an additional layer of quality and expertise to clinical programs through participant data reviews, protocol deviation assessments, and risk evaluations to aid mitigation efforts.
• Address clinical inquiries from all countries regarding marketed products or new submission dossiers. Help develop strategies to periodically update the clinical sections of core dossiers.
• Participate in the scientific review process during potential due diligence assessments of external opportunities, presenting and defending conclusions before appropriate committees.
• Participate in facilitating the compliance and contractual agreement to onboard Key Opinion Leaders (KOLs) and external experts, as well as steering advisory boards, and participate in scientific exchange meetings.

Who you are:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• You have a Bachelor’s Degree in Health Sciences or related field.
• You have 2+ years of experience as a Clinical Trial Scientist or 5+ years as a Clinical Program Leader (or equivalent).
• You possess significant experience in clinical document production and/or clinical trial feasibility and strategy, or related areas.
• You are fluent in both Spanish and English (C1.1 level or above).
• You have strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions. You interact effectively with key stakeholders across departments, divisions, and the company.
• You are an excellent team player and capable of working in cross-functional teams.
• You demonstrate a proactive approach, strategic thinking, and are result-oriented.
• You are available to travel occasionally.

What we offer:

It is a brilliant opportunity for you. Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at [website]. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!

We look forward to receiving your application!