Clinical Research Coordinator - Madrid

IQVIA; Madrid; Vor Ort; EUR 25.000 - 39.000; Teilzeit

Zusammenfassung

IQVIA in Madrid is seeking a part-time Clinical Research Coordinator to support an oncology trial on site, up to 18 hours per week for six months. This pivotal role involves assisting investigators, safeguarding subject safety, and ensuring smooth trial operations in a busy site environment.

You will handle study documentation, enrollment activities, data entry, and coordination with monitors and stakeholders, contributing to data quality and patient safety while adhering to study protocols and

Qualifikationen

• BS/BA in life sciences or equivalent and relevant experience.
• At least three years in oncology clinical trials.
• Strong knowledge of trial processes, CRFs, and study protocols.

Aufgaben

• Support clinical studies and maintain a safe study environment.
• Safeguard subjects' wellbeing and address concerns.
• Maintain study documents, CRFs, and EDC systems.
• Plan and coordinate procedures according to protocol.
• Assist with data entry, quality checks, and queries.
• Assist in enrollment by screening volunteers.
• Ensure correct custody of study drug per SOPs.
• Coordinate with study monitor on issues.

Kenntnisse

Clinical coordination

Oncology trials

Data entry

CRF management

MS Office

Ausbildung

BS/BA in life sciences

Tools

EDC systems

MS Excel

MS Word

Jobbeschreibung

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. We have a new part time project in Madrid for up to 18 hours per week (starting with 6 hours per week). It will be for 6 months and will support an oncology clinical trial on site in Madrid. 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 as a clinical research coordinator.
• At least three years of experience in oncology clinical trials.
• Excellent 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.

#LI-DNP #LI-CES #LI-HCPN #LI-CT1

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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.