Clinical Project Manager

Pfm; España; Presencial; EUR 90.000 - 140.000; Jornada completa

Descripción de la vacante

Precision for Medicine is hiring a (Senior) Project Manager with Oncology experience who has led full-service clinical trials in a CRO setting. You will oversee global studies (Ph I-IV), manage client relationships, and coordinate cross-functional teams to deliver on time, within scope and budget.

You bring 5–7 years in project management for clinical trials, strong GCP/ICH knowledge, exceptional communication in English, and proven ability to travel domestically and internationally.

Formación

• Degree or related life science qualification, or equivalent combination of education and experience.
• Previous experience in a full service/global Project Management role in the CRO industry.
• 5 to 7 years of industry experience and at least 4 years of full service Project Management experience in a clinical trial setting, working for a Clinical Research Organisation.
• Experience managing studies within Oncology.
• Working understanding of GCP/ICH guidelines and the clinical development process.
• Ability to travel domestically and internationally, including overnight stays.
• Effective communication in English, both written and spoken.
• Strong presentation skills.
• Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
• Proven ability to develop positive working relationships with individuals and teams internally and externally.
• Demonstrated understanding of medical terminology and clinical trial activities as they relate to the execution of a clinical development plan.

Responsabilidades

• Independently lead clinical projects in accordance with the study budget and scope of work, using strong interpersonal and organizational skills to set and achieve objectives; may be required to run international trials.
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations.
• Liaise with the Project Team and senior management of both Precision for Medicine and sponsors, including executive level.
• Handle and lead all aspects of one or more clinical research trials.
• Provide total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management, identifying key deliverables and performance metrics and escalation paths.
• Remain an active member of the Project Team with a focus on efficient management and execution of trials.
• Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets.

Conocimientos

Project management

GCP/ICH

Oncology trials

Client liaison

Cross-functional teams

Communication

Educación

Life science degree

Herramientas

CTMS

eTMF

EDC

IXRS

MS Project

PowerPoint

MS Office

Descripción del empleo

Overview

Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology? Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?

Precision for Medicine is looking to hire a (Senior) Project Manager with Oncology experience who has managed full service clinical trials within a CRO setting to join our global team. In this pivotal role you will have full service oversight for clinical projects across global/regional (Ph I-IV) trials within Oncology, accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality. You will be involved in all study stages, including proposal strategy, development, costing, and bid defence, and you will see studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout. You will work in a cross-functional team with internal and external stakeholders, driving quality and coordinating the study team.

We offer a high-energy, dedicated, collaborative environment with team members who enjoy a challenge and thrive in dynamic environments. If you are someone who takes charge and values positive teamwork to deliver excellent work, we have an opportunity for you.

Responsibilities

• Independently lead clinical projects in accordance with the study budget and scope of work, using strong interpersonal and organizational skills to set and achieve objectives; may be required to run international trials.
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations.
• Liaise with the Project Team and senior management of both Precision for Medicine and sponsors, including executive level.
• Handle and lead all aspects of one or more clinical research trials.
• Provide total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management, identifying key deliverables and performance metrics and escalation paths.
• Remain an active member of the Project Team with a focus on efficient management and execution of trials.
• Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets.

Qualifications

• Degree or related life science qualification, or equivalent combination of education and experience.
• Previous experience in a full service/global Project Management role in the CRO industry.
• 5 to 7 years of industry experience and at least 4 years of full service Project Management experience in a clinical trial setting, working for a Clinical Research Organisation.
• Experience managing studies within Oncology.
• Working understanding of GCP/ICH guidelines and the clinical development process.
• Ability to travel domestically and internationally, including overnight stays.
• Effective communication in English, both written and spoken.
• Strong presentation skills.
• Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
• Proven ability to develop positive working relationships with individuals and teams internally and externally.
• Demonstrated understanding of medical terminology and clinical trial activities as they relate to the execution of a clinical development plan.

Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, operational and medical authorities, biomarker and data analytics solutions, and a focus on rare diseases and oncology.

We are a people-focused CRO with a supportive and collaborative environment that promotes work-life balance and team development.

We invite you to learn more about our growing organization serving clients researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for their contributions every single day.

Compliance and Equal Opportunity

Data provided as part of this application will be stored in accordance with our privacy policy. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you require a reasonable accommodation to complete any part of the application process or need an alternative method for applying, you may contact Precision Medicine Group at myHR at precisionmedicinegrp dot com.

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