yandex
Страна
США
Зарплата
100 600 $ – 151 000 $
+500% приглашений

Откликайтесь
на вакансии с ИИ

Ускорим процесс поиска работы
УдалённоПолная занятость

Contract Manager - FSP

Оценка ИИ

Привлекательная вакансия с прозрачным диапазоном зарплаты и полным пакетом льгот. Удаленный формат работы и работа в инновационной сфере точной медицины делают предложение конкурентоспособным.


Вакансия из Quick Offer Global, списка международных компаний
Пожаловаться

Сложность вакансии

ЛегкоСложно
Оценка ИИ

Роль требует глубоких знаний в области клинических исследований (CTA) и не менее 5 лет специфического опыта. Высокая ответственность за соблюдение сроков исследования и юридическую чистоту документов повышает порог входа.

Анализ зарплаты

Медиана125 000 $
Рынок95 000 $ – 160 000 $
Оценка ИИ

Предложенный диапазон $100,600 – $151,000 полностью соответствует рыночным стандартам США для опытных менеджеров по контрактам в сфере клинических исследований (FSP/CRO). Верхняя граница диапазона выше средней по рынку, что отражает высокие требования к квалификации.

Сопроводительное письмо

I am writing to express my strong interest in the Contract Manager - FSP position at Precision Medicine Group. With over five years of experience in drafting and negotiating Clinical Trial Agreements (CTAs) and vendor contracts, I have developed a keen eye for detail and a deep understanding of the regulatory and operational timelines essential for successful clinical study execution. My background in managing site budgets and navigating complex legal frameworks aligns perfectly with the requirements of your Clinical Solutions team.

Throughout my career, I have excelled in fast-paced environments, ensuring that all legal agreements are in strict alignment with study milestones. I am particularly drawn to Precision Medicine Group's commitment to advancing precision medicine and would welcome the opportunity to apply my expertise in contract lifecycle management and stakeholder communication to support your FSP initiatives. I am confident that my proactive approach and ability to work effectively in a virtual environment will make me a valuable asset to your organization.

+250% к просмотрам

Составьте идеальное письмо к вакансии с ИИ-агентом

Составьте идеальное письмо к вакансии с ИИ-агентом

Откликнитесь в precisionmedicinegroup уже сейчас

Присоединяйтесь к лидеру в области точной медицины и управляйте ключевыми контрактами в клинических исследованиях — откликайтесь сейчас!

Описание вакансии

Position Summary:

Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements. Work closely with Clinical Operations study team and play a key role to ensure deliverables are in alignment with defined study timelines.

Essential functions of the job include but are not limited to:

  • Review, draft and negotiate a variety of agreements including master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts.
  • Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.
  • Ensure adherence to company policies, procedures and contracting standards.
  • Update relevant study team members regarding the status of contract negotiations and execution.
  • Establish, track, report and manage site contract metrics.
  • Support the maintenance of contract files and databases, including contract archiving.
  • Assist in designing and implementing policies and procedures to affect the timely execution of contracts.
  • Recognize where processes can be improved and take corrective action.
  • Other tasks as assigned.

Qualifications:

Minimum Required:

  • Graduate, postgraduate, 4-year college degree
  • Equivalent experience ideally in a scientific or healthcare discipline
  • Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, vendor contracts and site Budget negotiations, but no less than 5 years’ experience.
  • Experienced leading interactions with Study Teams and Sponsor

Preferred:

  • Bachelors in law, scientific fields, business administration or equivalent degree
  • Excellent organizational and communication skills and attention to detail
  • Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations
  • Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines

Skills:

Competencies

  • Possesses strong organizational/written communication skills and the ability to multi-task and prioritize in a fast-paced environment.
  • Executes time-sensitive matters while maintaining accuracy and attention to detail.
  • Exhibits high self-motivation and is able to work and plan independently as well as in a team environment.
  • Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills.
  • Displays sound business judgment and a proactive, independent work style.
  • Proficient in MS Office software programs and computer applications
  • Handles sensitive issues with discretion.
  • 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.

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

$100,600—$151,000 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.

+400% к собеседованиям

Создайте идеальное резюме с помощью ИИ-агента

Создайте идеальное резюме с помощью ИИ-агента

Навыки

  • Contract Management
  • Clinical Trial Agreements
  • Legal Drafting
  • Negotiation
  • Clinical Operations
  • Vendor Management
  • Budgeting
  • Microsoft Office
  • Stakeholder Management

Возможные вопросы на собеседовании

Проверка практического опыта ведения переговоров по специфическим для отрасли документам.

Опишите ваш опыт ведения переговоров по соглашениям о клинических исследованиях (CTA). С какими наиболее сложными пунктами вы сталкивались?

Оценка способности кандидата работать в условиях жестких дедлайнов клинических проектов.

Как вы приоритизируете задачи, когда несколько проектных команд одновременно требуют срочного согласования контрактов?

Проверка навыков финансового планирования в рамках контрактования.

Расскажите о вашем опыте ведения переговоров по бюджетам исследовательских центров. Как вы находите баланс между требованиями центра и бюджетом спонсора?

Оценка навыков взаимодействия с удаленными командами.

Как вы выстраиваете коммуникацию с мониторами (CRA) и проектными менеджерами в виртуальной среде для ускорения процесса подписания?

Проверка внимательности к деталям и знания стандартов.

Каков ваш процесс проверки контракта на соответствие внутренним политикам компании и стандартам качества?

Похожие вакансии

более 1000 офферов получено
4.9

1000+ офферов получено

Устали искать работу? Мы найдём её за вас

Quick Offer улучшит ваше резюме, подберёт лучшие вакансии и откликнется за вас. Результат — в 3 раза больше приглашений на собеседования и никакой рутины!

Страна
США
Зарплата
100 600 $ – 151 000 $