Sr CRA I home-based in Barcelona preferably. Sponsor dedicated

Syneos Health; Madrid; A distancia; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Senior Clinical Research Associate I to join their dynamic team. This role, ideally based in Barcelona, offers the opportunity to conduct vital site management activities, ensuring compliance with regulations and enhancing patient safety. You will work closely with passionate professionals dedicated to accelerating therapy delivery and improving lives. This is a fantastic opportunity for those looking to make a significant impact in the biopharmaceutical sector while enjoying a supportive and inclusive work environment that values career development and diversity.

Servicios

Career Development

Training and Recognition

Inclusive Culture

Diversity Initiatives

Formación

• Bachelor’s degree or RN in a related field, or equivalent experience.
• Knowledge of GCP / ICH and regulatory requirements.

Responsabilidades

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Manage project scope, timelines, and budgets at the site level.
• Serve as primary liaison with site personnel.

Conocimientos

GCP / ICH Knowledge

Communication Skills

Interpersonal Skills

Critical Thinking

Computer Proficiency

Educación

Bachelor’s Degree or RN

Descripción del empleo

Senior Clinical Research Associate I - Home-based in Barcelona (preferably) | Sponsor Dedicated

Join us at Syneos Health as a Senior Clinical Research Associate I . This role is ideally based in Barcelona, with a sponsor dedicated focus.

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About Syneos Health

Syneos Health is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We turn clinical, medical, and commercial insights into tangible outcomes to meet modern market demands.

Our Clinical Development model centers around the customer and patient, aiming to simplify and streamline our work for better collaboration and impact. Whether in a Functional Service Provider or Full-Service setting, you'll work with passionate problem solvers to help our clients achieve their goals. We are agile and committed to accelerating therapy delivery because we are passionate about changing lives.

Why Work Here?

• We invest in our people through career development, training, recognition, and rewards.
• We promote a Total Self culture, encouraging authenticity and inclusivity.
• We foster diversity of thought and background to create a sense of belonging for everyone.

Job Responsibilities

• Conduct site qualification, initiation, monitoring, management, and close-out visits (on-site or remote), ensuring compliance with regulations, ICH-GCP, GPP, and protocols. Evaluate site performance and escalate issues promptly.
• Verify informed consent processes and protect patient confidentiality. Assess safety and data integrity at investigator sites.
• Review source documents, verify data accuracy, and manage query resolution. Support electronic data capture and site compliance.
• Manage investigational product inventory, reconciliation, and storage security, ensuring proper dispensing per protocol.
• Maintain and reconcile Investigator Site Files and Trial Master Files, ensuring documentation accuracy.
• Document activities and support patient recruitment and retention strategies. Track progress and actions.
• Manage project scope, timelines, and budgets at the site level. Adapt to changing priorities.
• Serve as primary liaison with site personnel, ensuring training and compliance.
• Participate in meetings, support audit readiness, and mentor junior CRAs as needed.
• For Real World Late Phase (RWLP), hold the title of Sr. Site Management Associate I.

Additional Responsibilities

• Support sites throughout the study lifecycle, from identification to close-out.
• Develop and implement local informed consent forms.
• Collaborate with regulatory teams to ensure compliance.
• Participate in bid defense meetings and build relationships with sponsors and stakeholders.

Qualifications

• Bachelor’s degree or RN in a related field, or equivalent experience.
• Knowledge of GCP / ICH and regulatory requirements.
• Proficiency with computer systems and new technologies.
• Excellent communication and interpersonal skills, with basic critical thinking.
• Ability to travel up to 75% regularly.

Additional Information

This job description is not exhaustive. Responsibilities may change, and equivalent experience will be considered. We comply with applicable legislation and promote diversity and inclusion.

• Seniority Level : Mid-Senior level
• Employment Type : Full-time
• Job Function : Research and Science
• Industries : Biotechnology, Pharmaceutical Research, and Services