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Senior Project Manager - Clinical Trials
Отличная вакансия для опытных менеджеров: удаленная работа по всей Европе, фокус на социально значимых исследованиях (онкология) и работа в крупной международной CRO. Компания предлагает возможности для профессионального роста и участия в стратегических этапах развития проектов.
Сложность вакансии
Высокая сложность обусловлена требованием глубокой экспертизы в онкологии и минимум 4-летнего опыта управления полносервисными клиническими исследованиями именно в CRO. Роль подразумевает полную ответственность за бюджет, сроки и управление кросс-функциональными командами на глобальном уровне.
Анализ зарплаты
Зарплата для Senior Project Manager в Словакии в сфере клинических исследований обычно выше среднего по рынку труда страны, учитывая международный характер роли и узкую специализацию. Указанный диапазон соответствует рыночным стандартам для опытных специалистов в европейских CRO.
Сопроводительное письмо
I am writing to express my strong interest in the Senior Project Manager position at Precision for Medicine. With over six years of experience in clinical project management within the CRO industry and a specialized focus on complex Oncology trials, I am confident in my ability to lead full-service global studies to successful completion while maintaining high quality and budget standards.
Throughout my career, I have demonstrated a consultative approach to trial management, overseeing cross-functional teams including data management, safety, and biostatistics. My experience in bid defense and proposal strategy, combined with a deep understanding of GCP/ICH guidelines, aligns perfectly with the pivotal role you are looking to fill. I am particularly drawn to Precision for Medicine’s commitment to precision medicine and its supportive, people-focused culture.
I am eager to bring my expertise in managing international Phase I-IV trials to your global team and contribute to the development of life-changing therapies. Thank you for your time and consideration.
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Описание вакансии
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 are looking to hire a (Senior) Project Manager ideally with experience in Oncology who have 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 (or Rare Diseases or CNS). Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.
Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing 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 both internal and external stakeholders, driving quality and coordinating the study team.
We offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.
How we will keep you busy and support your growth:
- You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well.
- 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 Project Team and senior management of both Precision and sponsors, including C level
- Handle and lead all aspects of a clinical research trial or trials
- 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 of success and escalation.
- Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
- Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets
Requirements:
- Degree or similar related life science qualification, or equivalent combination of education and experience.
- Previous experience in a full service/global Project Management role working in the CRO industry is essential.
- 5 to 7 years industry experience and at least 4 years 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 drive and availability for domestic and international travel including overnight stays
- Be able to communicate effectively in the English language 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 individual and teams internally and externally
- Demonstrated core understanding of medical terminology and clinical trial activities as it relates 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, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
We are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development.
We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
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 are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
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Навыки
- Project Management
- Clinical Trials
- Oncology
- CRO
- GCP
- ICH Guidelines
- CTMS
- eTMF
- EDC
- IXRS
- Microsoft Project
- PowerPoint
- Medical Terminology
Возможные вопросы на собеседовании
Проверка опыта управления полным циклом исследования и взаимодействия с различными отделами.
Опишите ваш опыт управления полносервисными (full-service) исследованиями: как вы координируете работу отделов данных, безопасности и биостатистики?
Оценка навыков финансового менеджмента и контроля рисков.
Расскажите о случае, когда проект выходил за рамки бюджета или сроков. Какие меры вы предприняли для минимизации рисков и коммуникации с заказчиком?
Проверка специфических знаний в области онкологии, как того требует вакансия.
С какими основными сложностями вы сталкивались при проведении онкологических исследований (например, набор пациентов или специфические конечные точки) и как их решали?
Оценка опыта участия в коммерческой деятельности компании.
Какова была ваша роль в процессе подготовки предложений (RFP) и защите грантов (bid defense)?
Проверка лидерских качеств и умения работать с клиентами на высоком уровне.
Как вы выстраиваете отношения с C-level представителями спонсоров при возникновении конфликтных ситуаций в проекте?
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