Software Engineer (TypeScript) - Europe

Rollstack; Comunidad Valenciana; Presencial; EUR 50.000 - 70.000; A tiempo parcial

Descripción de la vacante

An industry-leading company is seeking a Clinical Research Coordinator to join their team in Valencia. This part-time position involves supporting clinical trials, ensuring compliance with study protocols, and maintaining effective communication with participants and investigators. The ideal candidate will have a background in life sciences and possess strong organizational and interpersonal skills. This role offers a unique opportunity to contribute to groundbreaking research while working in a collaborative and supportive environment. If you are passionate about clinical research and eager to make a difference, this position is perfect for you.

Formación

• Bachelor's degree in life sciences or equivalent experience in a clinical environment.
• Strong IT skills, especially in MS Office applications.

Responsabilidades

• Support clinical research studies and maintain a safe study environment.
• Assist with data entry, quality checking, and study enrollment.

Conocimientos

Interpersonal Skills

Organizational Skills

IT Competence

Knowledge of Medical Terminology

Knowledge of Clinical Trials

Educación

BS/BA in Life Sciences

Herramientas

MS Windows

MS Office (Access, Outlook, Excel, Word)

Descripción del empleo

Clinical Research Coordinator - Valencia, Spain

Apply locations : Valencia, Spain

Time type : Part time

Posted on : Posted 2 Days Ago

Job requisition id : R1464563

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 is looking for an experienced Clinical Research Coordinator for an upcoming project in Valencia on a part-time basis (24 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, as well as 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 subjects’ 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, or 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 clients.
• Good organizational skills with the ability to pay close attention to detail.