Clinical Research Associate II - Spain

Linical; Majadahonda; A distancia; EUR 42.000 - 64.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Home-based flexibility

International trials

Collaborative team

Competitive package

Descripción de la vacante

Linical is seeking an experienced Clinical Research Associate (CRA II) to manage investigative sites across Spain. The role offers home-based flexibility with up to 75% travel to sites, ensuring trials are conducted per protocol, ICH-GCP, and regulatory requirements.

You will lead site visits, protect patient safety, verify data integrity, and support TMF maintenance while working with cross-functional teams on international studies.

Formación

• Life Sciences degree or equivalent experience.
• Minimum 4 years' clinical research experience.
• Minimum 2 years' monitoring experience as a CRA.
• Strong knowledge of ICH-GCP, clinical trial regulations, and site management.
• Fluent in Spanish and English; Portuguese desirable.
• Excellent communication, organisation, and problem-solving skills.
• Ability to work independently and manage multiple priorities.
• Valid driver's license and willingness to travel up to 75%.

Responsabilidades

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure patient safety, data integrity, and protocol compliance.
• Perform source data verification and review study documentation.
• Manage site relationships and provide ongoing support to investigators and study staff.
• Assist with ethics committee and regulatory submissions where required.
• Monitor investigational product accountability and site performance.
• Maintain Trial Master File (TMF) documentation and support query resolution.
• Collaborate with cross-functional study teams to ensure successful trial delivery.

Conocimientos

CRA training

Monitoring

Site management

Data integrity

Communication

Travel ready

Educación

Life Sciences degree

Descripción del empleo

Are you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation?

We are seeking a CRA II to manage investigative sites across Spain, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.

• Ensure patient safety, data integrity, and protocol compliance.

• Perform source data verification and review study documentation.

• Manage site relationships and provide ongoing support to investigators and study staff.

• Assist with ethics committee and regulatory submissions where required.

• Monitor investigational product accountability and site performance.

• Maintain Trial Master File (TMF) documentation and support query resolution.

• Collaborate with cross-functional study teams to ensure successful trial delivery.

About You

• Life Sciences degree or equivalent experience, plus recognized CRA training.

• Minimum 4 years' clinical research experience.

• Minimum 2 years' monitoring experience as a CRA.

• Strong knowledge of ICH-GCP, clinical trial regulations, and site management.

• Fluent in Spanish and English languages, Portuguese is desirable

• Excellent communication, organisation, and problem-solving skills.

• Ability to work independently and manage multiple priorities.

• Valid driver's license and willingness to travel up to 75%.

What We Offer

• Home-based flexibility.

• Opportunity to work on international clinical trials.

• Collaborative and supportive team environment.

• Competitive salary and benefits package.