Clinical Study Coordinator

mAbxience; Córdoba; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A global biopharmaceutical company seeks a Clinical Study Coordinator to oversee clinical trials and manage CROs. Candidates should have a degree in Health Sciences, be fluent in English and Spanish, and possess at least 4 years of experience in the field. Attractive benefits include flexible hours, a permanent contract, and various insurances.

Servicios

Flexible start time

Permanent contract

Attractive salary package

Life and accident insurance

Ticket restaurant

Benefits and Savings Club

Development plans

Formación

• Minimum 4 years’ experience coordinating international clinical trials and managing CROs.
• Deep knowledge of international clinical trial regulations (ICH-GCP, FDA, EMA).
• Experience in oncology is a strong plus.

Responsabilidades

• Oversee and ensure the proper execution and follow-up of clinical trials.
• Design and manage clinical trial plans, identifying risks and implementing corrective actions.
• Ensure compliance with GCP, FDA, EMA, and ICH guidelines.

Conocimientos

Fluent in English

Fluent in Spanish

Strong organizational skills

Strong communication skills

Strong interpersonal skills

Educación

Degree in Health Sciences

Master’s degree

Descripción del empleo

In a nutshell 📌

Position

Clinical Study Coordinator

Location

Madrid, Hibrid

Experience

4+ years in international clinical trial coordination

Want to know more?

mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide.

What are we looking for?

• Oversee and ensure the proper execution and follow-up of clinical trials, managing CROs and vendors to meet timelines, quality standards, and regulatory requirements.
• Design and manage clinical trial plans, identifying risks and implementing corrective actions.
• Coordinate site and investigator selection, budget management, and vendor contracts.
• Ensure compliance with GCP, FDA, EMA, ICH guidelines, and internal procedures.
• Manage regulatory documentation and submissions, maintaining audit readiness.
• Supervise clinical trial monitoring, investigational product handling, and patient recruitment strategies.
• Collaborate with pharmacovigilance teams to ensure timely reporting and management of safety events.
• Support quality management through monitoring reports, deviation handling, and protocol amendments.
• Maintain effective communication with internal teams, CROs, investigators, and regulatory authorities.

What do you need?

• Degree in Health Sciences; Master’s degree is a plus.
• Fluent in English and Spanish; additional languages are an asset.
• Minimum 4 years’ experience coordinating international clinical trials and managing CROs.
• Deep knowledge of international clinical trial regulations (ICH-GCP, FDA, EMA).
• Experience in oncology is a strong plus.
• Strong organizational, communication, and interpersonal skills.
• Ability to work under pressure and prioritize tasks effectively.
• Willingness to travel up to 10%.

Our benefits!

• ⏰ Flexible start time from Monday to Friday (full-time).
• 📜 Permanent contract.
• 💸 Attractive salary package.
• 🥼 Life and accident insurance.
• 🍽️ Ticket restaurant
• 💸 Benefits and Savings Club.
• 📈 Development plans, internal mobility policy.
• ⭐ Many more!

What will the Selection process be like?

➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels.

➡️ Prepare well! We will continue with an in-person / virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test.

➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process.

Do you think this offer is not for you?

Follow us on social media like LinkedIn / Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting!

#mAbxience #ClinicalStudyCoordinator #BiotechCareers

COMMITMENT TO EQUAL OPPORTUNITIES

mAbxience is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of gender, ethnicity, religion, sexual orientation, disability, or any other characteristic.