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Spain

  • Lead global oncology clinical projects, managing full service oversight, budget, timelines, and cross-functional teams.
  • Serve as primary client liaison, drive proposal strategy, and ensure high-quality trial execution from start to finish.
  • Apply deep knowledge of GCP/ICH guidelines and use software like CTMS, EDC, and MS Project for efficient trial management.

Oncology Project Management Clinical Operations CTMS

10 jobs similar to Clinical Project Manager

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Europe

  • Manage and oversee all clinical aspects of trials across multiple countries, ensuring timeline adherence, quality, and scope.
  • Lead CRAs and collaborate with cross-functional teams to achieve high client satisfaction and smooth trial operations.
  • Identify risks, develop creative action plans, and maintain focus on study priorities through effective communication.

Precision for Medicine is a precision medicine CRO that combines novel trial designs, advanced biomarker analytics, and deep oncology expertise to accelerate drug development. The company fosters a dynamic, high-energy culture and values dedicated professionals who thrive in challenging environments.

Hong Kong Singapore Taiwan

  • Serve as primary point-of-contact and escalation point for clients, coordinating all functional services to meet timelines and budget.
  • Manage the study budget, financial health, and project profitability, ensuring compliance and accurate forecasting.
  • Develop robust project plans with risk management, maintain quality oversight, and lead internal and client meetings.

Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences, focusing on Oncology and Rare Disease. The company has an operational scale and expertise to bring life-changing therapies to patients.

US

  • Serve as primary point-of-contact and escalation point for clients, coordinating all functional services and external vendors.
  • Manage study budgets, project profitability, and billing compliance to ensure financial health and alignment with scope.
  • Develop robust project plans, track metrics, and prepare status updates for clients and senior management.

Precision Medicine Group is a global contract research organization specializing in oncology and precision medicine. The company values collaboration and quality, employing a diverse team of professionals dedicated to advancing clinical research.

Japan

  • Lead the delivery of complex global projects for clients within the contract research, life sciences, or regulated healthcare sectors.
  • Manage the full project lifecycle, including planning, execution, monitoring, reporting, delivery, and closure.
  • Coordinate cross-functional international teams and develop project plans, timelines, budgets, and resource allocation strategies.

Welo Life Sciences is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations in regulated global markets. It is a part of Welo Global brand, delivering solutions within a secure, audit-ready framework supported by seven ISO certifications.

Spain

  • You will monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
  • You will coordinate all activities to set up and monitor a study, including identifying investigators and preparing regulatory submissions.
  • You will travel domestically up to 50-60% for site visits and maintain fluency in English and local language.

Precision for Medicine is a clinical research organization focused on precision medicine for oncology and rare diseases. They are a smaller CRO with a strong culture and high employee retention.

US

  • Develop, mentor, coach and manage CTMs to progress their skillset per quality standards.
  • Collaborate with management to enhance CTM expectations and procedures for quality and efficiency.
  • Ensure CTMs have proper resources and training to deliver high-quality study conduct.

Precision for Medicine is a clinical research organization (CRO) that provides clinical trial management services. The company employs a large team of clinical research professionals and emphasizes quality and collaboration.

$80,000–$100,000/yr
US

  • Manage project scope, timeline, and delivery of quality products and services for clinical trials.
  • Align expectations and communicate effectively with stakeholders across internal teams and clients.
  • Track project financials, manage risks, and support continuous improvement initiatives.

eClinical Solutions provides expert data services and a clinical data cloud platform to accelerate clinical development for life sciences organizations. They are a fast-growing, people-first organization with a remote culture and have won Top Workplaces awards.

UK

  • Provide therapeutic and operational leadership throughout the clinical program and project delivery lifecycle.
  • Collaborate with cross-functional teams to develop effective delivery strategies and resolve operational challenges.
  • Ensure clinical projects within the assigned franchise are appropriately resourced and aligned with operational goals.

Our partner is a global clinical research organization dedicated to advancing healthcare innovation and improving patient outcomes through high-quality clinical trials. They offer a collaborative and inclusive environment with experienced professionals across global therapeutic and operational teams, focusing on professional growth and meaningful impact.

Global

  • Provide strategic oversight and leadership for a portfolio of complex global clinical trials in dermatology and rheumatology.
  • Serve as the key client contact, ensuring alignment on objectives, communication, and satisfaction throughout the study lifecycle.
  • Monitor budgets, timelines, risks, and quality while mentoring project managers and driving operational improvements.

The company is a specialized Contract Research Organization (CRO) focused on dermatology and rheumatology clinical trials. It fosters an international, collaborative, and science-driven environment with a commitment to operational excellence and innovation.

Poland

  • Monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
  • Coordinate all necessary activities to set up and monitor a study, including investigator identification, regulatory submissions, and pre-study/initiation visits.
  • Identify potential study risks, propose solutions, and handle conflict using resolution strategies while maintaining quality and attention to detail.

Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO that combines novel clinical trial designs, operational expertise, and biomarker analytics to advance oncology and rare disease treatments. The company fosters a culture with high CRA retention, small team influence, and a focus on work/life balance.