20 publicaciones de empleo destacadas en planning coordinator (¡Están contratando!)

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- Microsoft Powerpoint
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IE University —Madrid, Madrid provincia
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CHEP —Madrid, Madrid provincia
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- Microsoft Word
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- Microsoft Excel
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Project manager and roadmap coordinator
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Kenes Group Ltd —Madrid, Madrid provincia
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LOMARTOV S.L. —Burjassot, Valencia provincia
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PMO and Business Support Manager Aerostructures Programmes
Airbus Defence and Space SAU —Sevilla, Sevilla provincia
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- Project management
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Primary Special Educational Needs and Disabilities (SEND) Support
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BIM Coordinator
AECOM —Madrid, Madrid provincia
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- Español
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- Habilidades organizativas
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14d

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Country Coordinator - Clinical Research DCT (m/f/d ) - Remote

FutureMeds GmbH
En remoto

Solicitud rápida

Detalles del empleo

Contrato indefinido | Jornada completa
Hace 4 días

Cualificaciones

Francés
Inglés
Microsoft Office
Italiano

Descripción completa del empleo

Location: Spain, Romania, or Bulgaria

Required Languages: French, Italian and English (C1 level)

About FutureMeds @home

FutureMeds @home is part of the independent and fully owner‑managed FutureMeds European Site Network. We deliver high‑quality decentralized clinical trial (DCT) services with a strong focus on patient experience. Our mission is to accelerate access to life‑changing medicines by making clinical research more accessible and flexible for patients across Europe.

We are seeking a dedicated and organized Country Coordinator to join our Decentralized Operations team. This is a fully remote role open only to candidates based in Spain, Romania or Bulgaria who have the legal right to work in one of these countries.

Your Mission

As a Country Coordinator, you will support and guide Homecare Providers (HCPs) and clinical trial sites to ensure smooth execution of homecare visits (HCVs). You will act as a key liaison between sites, HCPs, and internal stakeholders, ensuring clear communication, high‑quality documentation, and compliance with all study and regulatory requirements.

Your work enables patients to participate in clinical trials with reduced burden by bringing clinical support directly to their homes.

Key ResponsibilitiesHomecare Provider (HCP) Identification and Training

Support internal database checks and selection of potential HCPs.
Collaborate with Talent Acquisition to initiate recruitment, interviews, and contracting steps.
Train and re‑train HCPs according to SOPs, study materials, and regulatory guidelines.

Site Contact and Training

Serve as the main point of contact for investigator sites.
Train sites on DCT services and processes to maximize participation.
Maintain ongoing communication regarding eligible patients, visit planning, and study updates.
Contribute to continuous improvement of site management and communication processes.

Homecare Visit Coordination

Confirm homecare visits with sites and collect required Physician Order Forms (POFs).
Ensure HCP availability and oversee planning of equipment and supply shipments.
Coordinate courier services when needed for samples or investigational medicinal products (IMPs).
Review source documents for accuracy and ensure timely submission to sites.
Complete follow‑up tasks and review HCP timesheets for Project Manager approval.

Documentation

Document all study-related activities within study‑specific systems (e.g., CTMS).
Support development of study documentation and shipment content lists.

Internal and External Communication

Maintain effective communication with clients, investigator sites, and HCPs.
Participate in internal and client meetings as required.
Escalate issues to Project Managers or Compliance leads when necessary.

Quality and Compliance

Adhere to FutureMeds SOPs, WIs, client expectations, and study specifications.
Contribute to quality oversight of homecare activities and source documents.
Ensure documentation of performance indicators and issues in internal systems.
Participate in CAPA processes and support continuous improvement initiatives.

What You Bring

Educational background in nursing or life sciences (preferred).
Excellent verbal and written communication skills.
Strong attention to detail and organizational abilities.
Ability to manage multiple priorities effectively.
Proficiency with MS Office applications.
Clinical trials or medical experience is an advantage.
Understanding of GDPR, ICH‑GCP, IATA, and regulated environments.
C1‑level proficiency in one or more of French, Italian and English (written and spoken).

Why Join Us?

Fully remote position available in Spain, Romania, or Bulgaria.
Work within an international, diverse team across Europe.
Contribute to the growing field of decentralized clinical trials and patient‑centric research.
Competitive salary and performance‑based bonus.
Opportunities for professional growth, training, and internal career development.
Occasional travel for internal meetings or events.

Job Types: Full-time, Permanent

Work Location: Remote

Solicitud rápida

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