- Страна
- США
- Зарплата
- 147 300 $ – 220 900 $
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на вакансии с ИИ

Senior Project Manager - Oncology
Отличная вакансия с прозрачным и конкурентным диапазоном зарплаты для рынка США. Компания предлагает сильный социальный пакет и возможность работать над передовыми проектами в области онкологии и клеточной терапии.
Сложность вакансии
Высокая сложность обусловлена требованиями к глубокому опыту в онкологии (7+ лет в КИ), управлению глобальными проектами и финансовой ответственности за бюджеты. Роль требует не только технических знаний GCP, но и лидерских качеств для ведения Bid Defense встреч.
Анализ зарплаты
Предложенный диапазон ($147k - $221k) полностью соответствует и даже несколько превышает среднерыночные показатели для Senior PM в крупных CRO и биотех-компаниях США, где медиана обычно составляет около $165k-$175k. Верхняя граница диапазона предполагает наличие исключительной экспертизы в онкологии.
Сопроводительное письмо
I am writing to express my strong interest in the Senior Project Manager position at Precision Medicine Group. With over 7 years of experience in clinical research and a proven track record of managing complex global oncology trials, I am confident in my ability to drive your projects to success while maintaining the highest standards of quality and financial health. My background aligns perfectly with your requirements for strategic planning, risk mitigation, and cross-functional leadership in the pharmaceutical and biotech sectors.
Throughout my career, I have successfully led multi-center trials, ensuring eTMF inspection readiness and managing budgets to maximize profitability without compromising clinical integrity. I am particularly drawn to Precision's focus on oncology and cell/gene therapy, areas where I have significant expertise and a deep commitment to advancing patient outcomes. I am eager to bring my negotiation skills and results-oriented mindset to your Clinical Solutions team and contribute to the continued growth of your global program.
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Описание вакансии
The Senior Project Manager plans, directs, coordinates, and delivers activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.
Essential functions of the job include but are not limited to:
- Serve as primary point-of-contact and primary escalation point to the client
- Coordinate and oversees all functional services including external vendors to the established timeline and budget
- Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate. Independently drive the CO to completion and execution with support as needed.
- Maintain integrated collaboration with clinical operations in the delivery and participates in clinical activities as appropriate. For projects of very limited scope (i.e. number of sites), Sr. PM may assume all clinical activities
- Manage the financial health of assigned studies, including oversight of the project profitability, billable project hours, and compliance with on time, accurate billing and forecasting to support business objectives.
- Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality
- Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings.
- Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation
- Establish tracking metrics to monitor trial and team progress towards project goals
- Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise
- Leads both internal and client meetings and set expectations for the project team
- Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues
- Ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients including Bid Defenses with proficiency
- Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project
- Support business development and marketing activities as appropriate, including travel to Bid Defense meetings as required
- Perform other duties as assigned by management
- Remain compliant with organizational training, time-reporting and any other administrative duties as required
- Provides on-going feedback, for functional team members including annual performance reviews
Qualifications:
Minimum Required:
- North America: Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred
- EU: Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred
- Minimum of 7 years of clinical research experience or proven competencies for this position and a minimum of 4 years of direct project management experience
- Experience in managing complex and global trials
- Ability to travel domestically and internationally including overnight stays
Other Required:
- Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) Microsoft Project, eTMF, EDC and CTMS
- Proven communication and interpersonal skills to effectively interface with others in a team setting
- Proven organizational skills, attention to detail, and a customer service demeanor
Competencies:
- Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as well as the ability to implement such items
- Direct work experience in a global, cross-functional project management environment
- Good understanding of cross-functional management
- Good understanding of project planning, risk management and change management with an awareness of appropriate escalation
- Proven experience in strategic planning, risk management and change management
- High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective
- Ability to lead and inspire excellence within a study team
- Ability to create an environment where study team members have a sense of ownership that will lead to increases in productivity and efficiency
- Results oriented, accountable, motivated and flexible
- Proven time management, negotiation, critical thinking, decision making, analytical and interpersonal skills
- Proven presentation, verbal and written communications skills
- Good understanding of project management software
- In depth proven experience in pharmaceutical and/or device research required
- Preferred: experience with oncology & cell and/or gene therapy
#LI-Remote
Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
$147,300—$220,900 USD
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
- Oncology Clinical Trials
- ICH-GCP
- eTMF
- EDC Systems
- CTMS
- Microsoft Project
- Risk Management
- Budget Management
- Change Management
- Clinical Operations
- Cell Therapy
- Gene Therapy
Возможные вопросы на собеседовании
Проверка опыта управления рисками в сложных международных проектах.
Опишите случай, когда глобальное клиническое исследование столкнулось с критическим риском. Какие превентивные меры вы предприняли и как это повлияло на бюджет?
Оценка навыков финансового менеджмента и контроля прибыльности.
Как вы подходите к управлению финансовым состоянием проекта и выявлению внеплановых (out-of-scope) активностей на ранних этапах?
Проверка готовности к защите заявок перед клиентами.
Расскажите о вашем опыте участия в Bid Defense. Какую стратегию вы используете для убеждения клиента в компетенциях вашей команды?
Оценка знаний в специфической области онкологии и клеточной терапии.
С какими специфическими сложностями вы сталкивались при управлении исследованиями в области онкологии или генной терапии по сравнению с другими терапевтическими областями?
Проверка лидерских качеств и управления командой.
Как вы обеспечиваете вовлеченность и чувство ответственности у членов кросс-функциональной команды в условиях удаленной работы?
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- Страна
- США
- Зарплата
- 147 300 $ – 220 900 $