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Manager, Site Contracts Management

Оценка ИИ

Отличная позиция для опытных менеджеров в сфере клинических исследований с возможностью полной удаленной работы из нескольких стран Европы. Компания является признанным экспертом в точной медицине, что обеспечивает профессиональный рост.


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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Роль требует глубоких знаний в области клинических исследований (CRO) и опыта ведения переговоров по контрактам на международном уровне. Управление удаленной командой и работа с крупными медицинскими учреждениями Северной Америки добавляют сложности.

Анализ зарплаты

Медиана5 500 €
Рынок4 500 € – 7 000 €
Оценка ИИ

Предлагаемая роль менеджера в международной CRO предполагает конкурентную оплату труда. Указанный диапазон соответствует рыночным ставкам для позиций уровня Manager/Senior Manager в сфере Clinical Operations в регионе Центральной и Восточной Европы.

Сопроводительное письмо

I am writing to express my strong interest in the Manager, Site Contracts Management position at Precision for Medicine. With extensive experience in Clinical Research Organizations and a proven track record of managing site contracts and budgets across Europe and North America, I am confident in my ability to lead your regional team and optimize the study start-up process.

Throughout my career, I have successfully managed remote teams of contract associates, ensuring the timely execution of Clinical Trial Agreements while maintaining high standards of accuracy and compliance. My expertise in negotiating complex agreements with major healthcare institutions, combined with a strategic approach to resource allocation and process improvement, aligns perfectly with the goals of your SSU Leadership team.

I am particularly drawn to Precision for Medicine's focus on oncology and rapid start-up initiatives. I am eager to bring my subject matter expertise to your organization and contribute to the delivery of life-changing treatments through efficient and effective contract management.

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Присоединяйтесь к лидеру в области точной медицины и возглавьте команду по управлению контрактами в Европе!

Описание вакансии

Precision for Medicine is looking for an experienced Manager, Site Contracts Management to join our European team. This position can be covered fully remotely from Poland, Slovakia, Hungary, Romania or Serbia.

Position Summary:

Work closely with Study Start Up, Clinical Operations, legal, HR, finance and other stakeholders to ensure Site Contracts team has all needed tools to deliver Site Contracts in the shortest possible time and play a key role to ensure all other deliverables of the Site Contracts group are in alignment with defined study timelines. This role will support to negotiations of contracts when needed and to deal with key clients. Will participate in corporate strategic initiatives for the Start Up group, such as Oncology Site Network and Rapid Start-up and will be part of the SSU Leadership.

Essential functions of the job include but are not limited to

• Review, update and/or establish process and procedures for overall site contract management in the organization at the regional level.

• Line manages a team of contract and budget associates.

• Allocate resources for new business in the organization, forecasting and planning current and expected work.

• Participate in discussions on resources needs and plan for the future on site contract’s structure.

• Report and manage contract metrics including productivity of the site contract’s function.

• Ensure adherence to company policies, procedures, and contracting standards.

• Escalate and resolve complex issues with legal, finance or supervisor.

• Review, draft, and negotiate a variety of agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements, ancillary agreements, and amendment agreements.

• Oversee execution of agreements at the portfolio level according to each study contract plan

• Oversee the maintenance of contract files and databases, including contract archiving.

• Recognize where processes can be improved and take corrective action.

• Assist in designing and implementing policies and procedures to affect the timely execution of contracts.

• Represent the organization as Subject Matter Expert in internal and external meetings including client meetings.

• Other tasks, as assigned.

Qualifications:

Minimum Required:

• 4-year college degree or equivalent experience ideally in a scientific or healthcare discipline

• Experience in Site Contracts departments in Clinical Research Organizations (CRO)

• Experience dealing with big health care institution in North America for performance/negotiations of clinical trials agreements.

• Experience in people management remotely.

Preferred:

• 5 years or more of relevant experience in drafting, reviewing, and negotiating Clinical Trial Agreements and site budgets, as well as management, control and tracking of the contract process at the project and at portfolio level.

• Experience in setting up Site Contracting Plans and exposure to Sponsors.

• Experience in different models of site contract’s structure.

Skills:

Competencies:

• Possesses strong organizational and written communication skills with attention to detail.

• Able to multi-task and prioritize in a fast-paced environment.

• Able to make things happen.

• Executes time-sensitive matters while maintaining accuracy and attention to detail. 

• Exhibits high self-motivation and can 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 including site budget planning tools.

• 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.

• Ability to drive and availability for domestic and international travel including overnight stays.

#LI-Remote

#LI-TB1

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

  • Clinical Research
  • Contract Management
  • Clinical Trial Agreements
  • Negotiation
  • People Management
  • Budgeting
  • Microsoft Office
  • Legal Compliance
  • Study Start-Up
  • CRO

Возможные вопросы на собеседовании

Проверка опыта управления распределенными командами в разных часовых поясах.

Расскажите о вашем опыте линейного руководства командой по контрактам в удаленном формате: как вы контролируете метрики и поддерживаете мотивацию?

Оценка навыков ведения переговоров в сложных условиях.

Опишите случай, когда переговоры по бюджету или условиям CTA с крупным медицинским центром зашли в тупик. Как вы разрешили ситуацию?

Проверка понимания специфики CRO и стартапов исследований.

Какие стратегии вы используете для сокращения сроков этапа Study Start-Up при сохранении качества комплаенса?

Оценка умения работать с ресурсами и прогнозированием.

Как вы подходите к распределению ресурсов и планированию нагрузки в команде при поступлении нескольких новых проектов одновременно?

Проверка технических знаний и работы с документацией.

С какими типами вспомогательных соглашений (ancillary agreements) вы работали чаще всего и какие юридические риски в них наиболее критичны?

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