Clinical Research Associate Trainee

Theradex Oncology; España; A distancia; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading Contract Research Organization is hiring a Full-time Permanent CRA (Trainee) in Spain. This role offers an entry into multiple career pathways within the pharmaceutical industry and requires fluency in Spanish and English, plus a second European language. Candidates should have a relevant bachelor's degree and strong communication skills. The position involves up to 70% travel and is set in a friendly and supportive culture.

Servicios

Friendly and supportive culture

Formación

• Previous experience with Clinical Research Site Coordination or related fields preferred.
• Study Start up experience is an advantage.
• Ability to work independently as well as in a group.

Responsabilidades

• Travel up to 70% nationally and internationally to meet study requirements.
• Work in a remote environment addressing minor technical challenges.
• Absorb and apply knowledge gained through training on assigned protocols.

Conocimientos

Fluent in Spanish

Fluent in English

Good communication skills

Strong interpersonal skills

Educación

Bachelor's degree in biological or human science-related field

Oncology knowledge / PhD preferred

Herramientas

Microsoft Outlook

Microsoft Word

Microsoft Excel

Descripción del empleo

Overview

Hiring a Full time Permanent CRA (Trainee) in the Spain (Home based)

What in it for you

The CRA trainee program offers talented applicants an entrance ticket to many career pathways within the pharmaceutical industry. Theradex Oncology is a full-service Contract Research Organization (CRO). Theradex assists the pharmaceutical industry with the complete set of services that is required to bring a product from first-in-man to market registration. Talented candidates are able to reach the Senior CRA position from the CRA trainee program. Other career pathways may subsequently be available within the full service offering to our clients. We encourage applications by multi-language applicants. This role requires fluency in Spanish, English language, plus a second European language of either Dutch or French is preferred.

Qualifications

• Level of Education: At minimum, Bachelor\'s degree (BSc, BA, or RN equivalent) in biological or human science-related field or equivalent experience.
• Oncology knowledge / PhD preferred

Prior Experience

• Previous experience with Clinical Research Site Coordination or related fields (i.e. Regulatory Specialist) preferred.
• Previous experience in monitoring (i.e. In-House CRA / CTA / CMA) or equivalent experience) preferred.
• Study Start up experience is an advantage

Additional Requirements

• This position involves international and / or national travel as needed to meet study requirements. Ability to travel domestically and / or internationally and may involve overnight stays. Travel requirements are up to 70%.
• Valid Driver\'s License preferable.
• Passport essential
• Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements.
• Fluent in English, Spanish and another European language is preferred

Skills and Competencies

• Professional attitude with good customer focus.
• Strong communication skills : verbal / written / presentation.
• Good interpersonal skills, including persuasion and influence.
• Able to work independently as well as in a group.
• Good time management, multitasking and execution skills.
• Good organizational skills, including efficiency, punctuality, and collaboration in a team environment.
• Demonstrated proficiency in Microsoft Outlook, Word, and Excel.
• Technically proficient enough to work in a remote environment and able to address minor technical challenges without support but will timely escalate to Information Technology Support for challenges beyond capabilities.
• Capable of absorbing and applying knowledge gained through internal and external trainings on protocols assigned.
• Knowledge of ICH Guidelines and GCP including an understanding of regulatory requirements.
• Effective knowledge of the drug development process and the Theradex organizational structure

What we offer

We offer a friendly and supportive culture that puts people first.

This job does not offer company sponsorship

Theradex is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment.