- Страна
- США
- Зарплата
- 68 700 $ – 103 100 $
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на вакансии с ИИ

Senior Contract and Budget Associate
Позиция предлагает конкурентную заработную плату, полную удаленку и отличный пакет льгот в стабильной отрасли Life Sciences. Четко прописанные обязанности и возможность карьерного роста через менторство делают вакансию привлекательной.
Сложность вакансии
Роль требует глубоких знаний в области юридических аспектов клинических исследований и опыта ведения переговоров с международными институтами. Высокая ответственность за соблюдение сроков и точность бюджетов повышает сложность позиции.
Анализ зарплаты
Предложенный диапазон ($68,700 — $103,100) полностью соответствует рыночным стандартам США для позиции Senior Associate в сфере клинических исследований. Нижняя планка подходит для специалистов с минимально требуемым опытом (3 года), в то время как верхняя граница отражает оплату для экспертов с глубокой специализацией.
Сопроводительное письмо
I am writing to express my strong interest in the Senior Contract and Budget Associate position at Precision Medicine Group. With over three years of experience in drafting and negotiating Clinical Trial Agreements (CTAs) and Confidentiality Disclosure Agreements (CDAs), I have developed a keen eye for detail and a deep understanding of the contractual complexities inherent in the life sciences industry. My background in managing site budgets and interacting with both North American and European institutions aligns perfectly with the requirements of this role.
Throughout my career, I have demonstrated the ability to work independently in virtual environments, ensuring that all deliverables meet strict project timelines without compromising accuracy. I am particularly drawn to this opportunity because of Precision's reputation for excellence in clinical research and the chance to mentor junior associates. I am confident that my proactive approach to contract management and my commitment to maintaining high professional standards will make me a valuable asset to your Clinical Operations team.
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Описание вакансии
Position Summary:
Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations.
Essential functions of the job include but are not limited to:
• Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendorcontracts and site budgets.
• Lead interactions with the North American and European internal study teams, as applicable
• Lead interactions regarding the various agreements with the Site(s)
• Lead interactions regarding assigned agreements with the Sponsor(s)
• Work with supervisor and various internal/external stakeholders to resolve contractual issues.
• Ensure adhered to company policies, procedures, and contracting standards.
• Update relevant study team members and sponsors regarding the status of contract negotiations and execution.
• Coordinate execution of the agreements
• Support the maintenance of contract files and databases, including email and document archiving.
• Other duties as assigned.
Qualifications:
Minimum Required:• Bachelor’s degree, or equivalent contract management experience preferably in a clinical
research or similar industry setting
Other Required:
• 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as well as management, control and tracking of the contract process.
• Experience in contract research, life science, biotech or pharmaceutical industry is preferred.
• Experience interacting with European institutions.
Preferred:
• Equivalent contract management experience in a clinical research or similar industry setting
• Experience in contract research, life science, biotech or pharmaceutical industry.
Skills:
Competencies
• Excellent organizational and communication skills and attention to detail
• Experience in tracking status for site contracts and budget, filing and distribution.
• Executes time-sensitive matters while maintaining accuracy and attention to detail.
• Exhibits high self-motivation and is able to work and plan independently or with limited supervision.
• Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments and understanding of the service culture and positive interactions with customers.
• Proficient in MS Office Software programs and computer applications
• Works well independently and cooperatively with others to achieve common goals in a virtual environment.
• Develops, maintains and strengthens relationships with others inside or outside of the organization who can provide information, assistance and support Mentor and/or Ambassador for new Contract and Budget Associates and PFM staff
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
$68,700—$103,100 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
- Contract Management
- Clinical Trial Agreements
- Budgeting
- Legal Drafting
- Negotiation
- Microsoft Office
- Clinical Research
- Life Sciences
- Confidentiality Agreements
Возможные вопросы на собеседовании
Проверка практического опыта работы со специфическими документами отрасли.
Опишите ваш опыт ведения переговоров по договорам о клинических исследованиях (CTA). С какими наиболее сложными пунктами вы сталкивались?
Вакансия предполагает работу с европейскими и североамериканскими командами.
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Важная часть роли — управление бюджетами сайтов.
Расскажите о вашем процессе разработки и согласования бюджетов для клинических центров. Как вы обеспечиваете их соответствие рыночным стандартам?
Работа удаленная и требует соблюдения жестких графиков.
Как вы расставляете приоритеты при одновременной работе над несколькими контрактами для разных протоколов исследований?
В описании указана роль наставника.
Был ли у вас опыт обучения или менторства новых сотрудников в области контрактного менеджмента? Каков был ваш подход?
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- Страна
- США
- Зарплата
- 68 700 $ – 103 100 $