Clinical Project Manager

Precisionscientia; Barcelona; A distancia; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company in clinical research is seeking an experienced Clinical Project Manager to oversee global oncology trials. The successful candidate will be responsible for project management, client interactions, and ensuring compliance with industry standards. This role requires a strong background in life sciences and substantial project management experience in the CRO field.

Formación

• 5-7 years industry experience with at least 3 years in clinical project management at a CRO.
• Experience managing Oncology studies.
• Willingness to travel domestically and internationally.

Responsabilidades

• Lead all stages of clinical studies, including proposal development and full-cycle management.
• Manage client relationships and project teams.
• Prepare and present project status updates to clients and management.

Conocimientos

Interpersonal skills

Knowledge of GCP / ICH guidelines

Clinical trial management

Project management

Fluency in English

Educación

Degree in life sciences

Herramientas

MS Office

MS Project

CTMS

eTMF

EDC

IXRS

Descripción del empleo

Clinical Project Manager / Senior Clinical Project Manager

Remote, Spain

Are you an experienced full-service Project Manager in the field of clinical trials with a focus on Oncology? Are you passionate about impacting patient health and lives worldwide? Do you take a consultative approach to trial management, serving as a valuable partner in operational delivery?

Precision for Medicine (CRO) seeks to hire a (Senior) Project Manager, preferably with Oncology experience, who has managed full-service clinical trials within a CRO setting to join our global team.

Role Overview

You will oversee clinical projects across global / regional (Ph I-IV) trials within Oncology (or Rare Diseases or CNS). Your responsibilities include ensuring timely delivery, managing functional departments, and maintaining scope, cost, and quality standards.

Key Responsibilities

• Lead all stages of clinical studies, including proposal development, budgeting, and full-cycle management.
• Manage client relationships and project teams, ensuring clear communication and delivery.
• Coordinate across functional areas such as data management, safety, and biostatistics.
• Prepare and present project status updates to clients and management.
• Develop and review study documentation, including protocols, plans, and budgets.

Requirements

• Degree in life sciences or equivalent experience.
• 5-7 years industry experience with at least 3 years in full-service clinical project management at a CRO.
• Experience managing Oncology studies.
• Knowledge of GCP / ICH guidelines and clinical development process.
• Willingness to travel domestically and internationally.
• Fluent in English, both written and spoken.
• Proficiency in MS Office, MS Project, and relevant clinical trial software (CTMS, eTMF, EDC, IXRS).
• Strong interpersonal skills and understanding of medical terminology related to clinical trials.

About Us

Precision for Medicine combines innovative trial designs, leading operational and medical expertise, advanced biomarker and data analytics, with a passion for rare diseases and oncology. We foster a supportive, collaborative environment that promotes work-life balance and professional growth.

Application Process

Please fill out the application form, including your personal details, resume, education, desired salary, work authorization status, and previous employment with us or our affiliates. Ensure all information is accurate and complete. By submitting, you consent to data retention in accordance with our Privacy Policy.

J-18808-Ljbffr

J-18808-Ljbffr