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США
Зарплата
68 700 $ – 103 100 $
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SeniorУдалённоПолная занятость

Senior Contract and Budget Associate

Оценка ИИ

Стабильная позиция в крупной международной компании с прозрачной вилкой оплаты и полным пакетом льгот. Удаленный формат работы и узкая специализация делают вакансию привлекательной для экспертов в области клинических исследований.


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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Роль требует специфического опыта в сфере клинических исследований (CRO/Pharma) и навыков ведения юридических переговоров. Основная сложность заключается в необходимости координировать процессы между спонсорами и исследовательскими центрами в разных юрисдикциях (США и Европа).

Анализ зарплаты

Медиана85 000 $
Рынок70 000 $ – 110 000 $
Оценка ИИ

Предложенный диапазон ($68,700 — $103,100) полностью соответствует рыночным ожиданиям для позиции Senior уровня в США. Нижняя планка подходит для специалистов с минимально требуемым опытом (3 года), в то время как верхняя граница конкурентоспособна для экспертов с глубоким знанием индустрии.

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 legal and financial complexities inherent in clinical research. 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 a virtual environment while maintaining high standards of accuracy under tight deadlines. I am particularly drawn to Precision Medicine Group's commitment to advancing medicine and would welcome the opportunity to apply my expertise in contract management to support your Clinical Operations team. I am confident that my proactive approach and professional communication skills will contribute to the efficient execution of agreements and the overall success of your global studies.

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Присоединяйтесь к команде Precision Medicine Group и станьте ключевым звеном в запуске инновационных клинических исследований!

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 Research
  • Legal Drafting
  • Negotiation
  • Clinical Trial Agreements
  • Budgeting
  • Microsoft Office
  • Communication Skills
  • Project Management

Возможные вопросы на собеседовании

Проверка практического опыта работы со специфическими документами отрасли.

Расскажите о вашем опыте ведения переговоров по договорам о клинических исследованиях (CTA). С какими наиболее сложными пунктами вы сталкивались?

Оценка способности работать с финансовой составляющей контрактов.

Как вы подходите к разработке и согласованию бюджетов исследовательских центров, чтобы обеспечить соответствие рыночным стандартам и требованиям спонсора?

Важно для работы в международной среде, указанной в вакансии.

Был ли у вас опыт взаимодействия с европейскими медицинскими учреждениями? Какие культурные или правовые особенности вы учитывали при переговорах?

Проверка навыков тайм-менеджмента в условиях многозадачности.

Как вы приоритизируете задачи, когда одновременно ведете несколько десятков контрактов на разных стадиях согласования?

Оценка навыков решения конфликтов между сторонами.

Опишите ситуацию, когда спонсор и исследовательский центр не могли прийти к соглашению по условиям договора. Как вы помогли найти компромисс?

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68 700 $ – 103 100 $