Clinical Research Coordinator - Malaga, Spain

IQVIA; Málaga; Presencial; EUR 21.000 - 34.000; A tiempo parcial

Descripción de la vacante

IQVIA is seeking a part-time Clinical Research Coordinator in Málaga to support a single site with 10 hours per week. You will assist investigators, manage study documents, and help ensure protocol adherence and data quality.

The role requires a life sciences background, familiarity with clinical trials, and strong IT and interpersonal skills to coordinate with the study team and volunteers.

Formación

• BS/BA in life sciences or equivalent and/or relevant clinical experience.
• Basic knowledge of clinical trials and study procedures.
• Strong IT skills with MS Office.
• Excellent interpersonal and organizational skills.
• Ability to recruit, screen and orient volunteers per protocol.

Responsabilidades

• Support clinical research studies and maintain a safe study environment.
• Safeguard the well-being of subjects and address concerns.
• Maintain study protocols, CRFs, EDC systems and related documents.
• Plan and coordinate logistical activity for study procedures.
• Prepare for study procedures including labeling tubes and inventory.
• Assist with data entry, quality checks and query resolution.
• Assist in study enrollment by recruiting and screening volunteers.
• Ensure correct custody of study drug per SOPs.
• Coordinate with study monitor and respond to questions.

Conocimientos

IT proficiency

Interpersonal skills

Organizational skills

Attention to detail

Educación

BS/BA in life sciences or equivalent

Herramientas

MS Windows

MS Excel

MS Word

Access

Descripción del empleo

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator in Malaga to work at one site for 10 hours per week.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator

• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns

• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents

• Plan and coordinate logistical activity for study procedures according to the study protocol

• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues

• Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness

• Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol

• Correct custody of study drug according to site standard operating procedures

• Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession

• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

• Basic knowledge of medical terminology

• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client

• Good organizational skills with the ability to pay close attention to detail.

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IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.