Sr Clinical Project Manager

Crovelis

Madrid

On-site

EUR 50,000 - 70,000

Full time

14 days+

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Job summary

Crovelis busca un/a Gerente de Proyecto Clínico Senior para dirigir ensayos clínicos en Madrid. El candidato ideal tiene un grado en Ciencias de la Vida y más de 5 años de experiencia en investigación clínica. Esta posición implica la gestión de equipos multifuncionales y la responsabilidad de la ejecución conforme a las regulaciones ICH-GCP. Se requiere liderazgo, habilidades de comunicación efectiva, y fluidez en inglés, con un interesante paquete de beneficios y tecnología de vanguardia a disposición.

Qualifications

5+ años en investigación clínica, al menos 2 años en un rol de CPM/Clinical Ops Lead.
Conocimiento profundo de ICH-GCP, operaciones de ensayo, presupuestación, manejo de proveedores y sistemas clínicos.

Responsibilities

Liderar la entrega completa de ensayos, colaborando con equipos multifuncionales.
Coordinar la planificación del ensayo incluyendo líneas de tiempo, presupuestos y planes de comunicación.

Skills

Liderazgo

Comunicación

Toma de decisiones basada en datos

Multitarea

Fluidez en inglés

Education

Grado en Ciencias de la Vida, Farmacia o relacionado

Job description

Crovelis Madrid, Community of Madrid, Spain

Sr Clinical Project Manager

Crovelis Madrid, Community of Madrid, Spain

3 days ago Be among the first 25 applicants

Join Crovelis as a Senior Clinical Project Manager

Crovelis, a pioneering AI-powered CRO, is a proud member of the Exeltis family—an innovative global pharmaceutical division of Insud Pharma. Exeltis boasts nearly 4,000 professionals across 40+ countries, with 300+ products focused on women’s health, CNS, respiratory, cosmetic, and ophthalmic therapies. At Crovelis, we combine this strong pharmaceutical legacy with intelligent technology to redefine clinical research.

As a Senior Clinical Project Manager, you'll:

Lead end‑to‑end trial delivery, collaborating closely with Clinical Ops Managers/Senior Trial Managers, CRAs, and clinical sites from feasibility to trial close‑out.
Provide dedicated clinical leadership, advancing trial goals while ensuring on-time, on-budget, and ICH‑GCP compliant execution.
Coordinate multi-functional teams—clinical, PV, data, biostats, regulatory, QA, medical, and CROs/vendors.
Own trial planning including timelines, budgets, risk & communication plans, KPIs, and tool-based tracking.
Oversee start-up tasks: feasibility, site selection, contracts, ethics/regulatory approval, and IP handling.
Manage monitoring visits, safety reporting, data validation, audit readiness, documentation, and final reporting.
Select, onboard, and monitor CROs/vendors, ensuring KPI compliance and quality assurance.
Lead kick-off, investigator, and vendor meetings, and ensure team training and regulatory audit readiness.
Identify and mitigate trial risks, proactively communicating updates to all stakeholders.
Keep up with industry trends and integrate best practices and technologies into project delivery.

What You’ll Bring

Degree in Life Sciences, Pharmacy, or related—Master’s or higher is a plus.
5+ years in clinical research with at least 2 years in a Senior CPM/Clinical Ops Lead role (Pharma or CRO).
In-depth knowledge of ICH‑GCP, trial operations, budgeting, vendor management, and clinical systems.
Strong leadership, communication, data-driven decision-making, and multi-tasking skills.
Fluent in English; additional languages are advantageous.
Willingness to travel (~30%).
A cutting-edge AI-enhanced CRO backed by Exeltis’s global pharmaceutical strength.
Access to industry-leading technology and a foundation of 300+ established products .
Engage in meaningful, innovative research benefiting from very agile and collaborative culture.
Shape clinical trial strategy in a transparent, value-driven environment that prioritizes quality, integrity, and speed.

Seniority level

Seniority level
Mid-Senior level

Employment type

Employment type
Full-time

Job function

Job function
Health Care Provider
Industries
Research Services

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