Вакансии для хороших наёмных менеджеров

К 90-то летию гениального русского художника Анатолия Зверева, Музей AZ учреждил премию ZVEREV ART PRIZE и объявил имена 50-ти номинантов, работы которых будут представлены на выставке в Новом Манеже с 6 сентября по 3 октября 2021 года. Выставка включит в себя 50 работ современных художников, созданных специально для Премии. Сейчас организаторы проекта приглашают Волонтеров-медиаторов стать частью этого уникального и исторического события.   Это огромный опыт работы в музейном пространстве и возможность попробовать себя в новой профессии, познакомиться с такими же увлеченными людьми, завести новых друзей.   Условия: Все волонтеры получат благодарственные письма и памятные подарки от Музей AZ, станут друзьями музея и будут посещать все мероприятия музея бесплатно.
Если у вас есть волонтерская книжка, в ней будет сделана соответствующая запись.
Если вы студент искусствовед или культуролог, могут оформить вам прохождение практики или стажировки в Музее.

Интересная возможность для талантливых Дизайнеров поучаствовать в конкурсе ювелирных украшений Новая Реальность.   Ищут свежие дизайны, яркие идеи и новые решения.   Условия участия: Создайте эскиз ювелирных украшений от руки или на компьютере. Это может быть одно изделие, сэт (до 3-х изделий) или целая коллекция.
Продумайте название, описание, свои рекомендации по материалам, цветам, камням к своему украшению или украшениям.
Вы можете прислать неограниченное количество эскизов, каждый эскиз оформляется отдельной заявкой.   Приз: Участие в конкурсе бесплатное, призовой фонд — 180 000 рублей.   Дедлайн для участников — 30 сентября 2021 года.

Россельхозбанк  заинтересован в откликах кандидатов на вакансию Исполнительный директор управления проектного менеджмента.   Обязанности:
Выстраивание процессов управления внедрением изменений в Jira (проектная деятельность, гибкие методики внедрения в связке с производственным циклом по автоматизации и другими задачами);
Выполнение роли Владельца продукта по проектным областям в Jira;
Глубокое знание JIRA и Confluence, плагинов ALM Works;
Опыт внедрения/администрирования JIRA в крупных организациях;
Консультирование и помощь пользователям при их практической работе в системе;
Проработка и детализация новых/существующих задач в бэклоге;
Подготовка необходимых отчётов о работе системы;
Подготовка предложений по использованию плагинов для продуктов Jira и Confluence для реализации того или иного функционала;
Моделирование работы системы на стендах и в необходимых случаях ручное тестирование нового/доработанного функционала;
Обработка обращений на 3-ю линию поддержки, разбор и устранение дефектов, связанных или вызванных релизами системы;
Самостоятельная подготовка и выполнение доработок системы в соответствии с действующими нормативными документами, стандартами и правилами работы;
Участие во внедрении Confluence;
Организация полного цикла системного анализа, настройки/разработки, тестирования и подготовки к развёртыванию необходимого функционала системы;
Подготовка предложений и спецификаций по повышению стабильности, отказоустойчивости, быстродействию, совершенствованию среды разработки и тестирования, архитектуры системы;
Подготовка и согласование эксплуатационной документации (инструкции, регламенты и др.);
Проведение настроек в тестовой среде и среде разработки;
Разработка и согласование ТЗ, БФТ, ФТ на доработку системы;
Подготовка спецификаций для разработчиков;
Разработка и согласование ПМИ и тестовых сценариев;
Подготовка поставки с пошаговыми указаниями для переноса изменений в промышленную среду;
Составление план-графика и организация переноса в промышленную среду;
Участие в ПСИ;
Следование установленным внутренним стандартам по подготовке изменений ПО.   Требования:
Высшее экономическое\ высшее техническое образование;
Уверенный пользователь MS Office – обязательно: Excel – на уровне макросов, Visio, PowerPoint – свободное владение навыками разработки презентационных материалов;
Глубокое знание JIRA и Confluence, плагинов ALM Works;
Опыт внедрения/администрирования JIRA в крупных организациях.

MANGO OFFICE — одна из крупнейших компаний страны, известный поставщик IT решений для бизнеса и один из лидеров российского рынка виртуальных АТС, открывает вакансию Руководитель службы маркетинга.   Обязанности:
Формирование маркетинговой стратегии компании (прежде всего digital) на 1-3-5 лет;
Бюджетирование, контроль использования маркетингового бюджета;
Выстраивание омниканальных процессов в маркетинге;
Разработка стратегии по коммуникации с брендами, рекламными агентствами, блогерами, партнерами и иными участниками телеком-рынка;
Формирование контент-плана для всех площадок;
Формирование плана и контроль за организацией event-деятельности компании;
Контроль за разработкой всей BTL-продукции компании;
Управление репутацией компании и NPS;
Планирование PR-деятельности компании;
Разработка предложение по УТП, креативам, акциям;
Ежемесячная/годовая отчетность, трекинговая и ad-hoc аналитика   Требования:
Опыт выстраивания бизнес-процессов в маркетинге и со смежными департаментами;
Опыт формирвания команды профессионалов;
Мочь и уметь вовлекать и мотивировать сотрудников на командную работу.

TikTok is seeking a Talent Acquisition Lead.   The Talent Acquisition Lead will be responsible for managing the full lifecycle of a hiring process including; intake meeting, sourcing, and offer stage while also being a business partner to key stakeholders across the business. You will build innovative sourcing strategies led by data and market intelligence, lead a selection process that adopts D&I best practices, and ensure exceptional candidate experience through the hiring journey.   Responsibilities: Partner closely with business units to ensure sourcing and hiring strategies are aligned with TikTok people strategies. Partner with business leaders and hiring managers to assess their talent requirements and advise on the best hiring strategy. Use various techniques, skills, and experience to discover, identify, and attract top talent. Screen and select candidates effectively by assessing both the technical or business skills as well as the culture fit with the TikTok environment. Provide an efficient and high-touch experience for every candidate from the application stage to offer, evaluating skill level, driving the interview and offer process, including reference checks, salary recommendations, and closing of candidates.   Qualifications: Bachelor degree or above in in Human Resources related field. Fluent in English and Russian. Keen attention to detail, and experience in both building and executing recruiting processes, 3+ years of in-house recruitment experience. Strong interpersonal skills with the ability to build rapport quickly with employees and communicate effectively with all levels of the organization. Optimistic and collaborative — we’re building an awesome team and looking for someone excited to roll their sleeves up and join us as we start this journey. Entrepreneurial and creative problem-solving ability — you’ll have lots of support but often have to figure out the solution yourself. Experience closing all levels including senior and/or executive-level candidates and negotiating complex compensation packages. Passionate about providing a great experience for all our candidates including the unsuccessful ones.

TikTok ведет поиск Russia product strategy and operations lead-а.   Responsibilities
As an experienced product marketing professional, you will lead the go-to market strategy for our ad products in Russia. By partnering closely with various cross-functional stakeholders in sales, product management and business marketing, you help advertisers achieve their marketing goals by bringing our performance advertising solutions to them. An ability to self-motivate, prioritize and influence partners are key skills. You must have experience working with advertising products and have strong project management capabilities   Responsibilities: • Partner closely with Sales team to deeply understand businesses pain points, form business requirements and prioritize solutions to influence the direction of product development. • Partner with cross-functional teams to develop and execute regional programs and initiatives. • Define go-to-market (GTM) strategy for TikTok’s ever-evolving ads product. Instrumental in setting go-to-market strategy, and ensuring flawless execution and operations against the strategy. • Build an understanding of the most nascent TikTok advertising and measurement products and leverage these products to achieve customer goals. • Prioritize, distill and surface market intelligence to shape future advertising products.   Qualifications: • BA/BS degree or above. • 5+ years of product / performance marketing or product management experience with digital ad products. • 3+ years of experience from the digital advertising industry. • Strong knowledge of sales and marketing processes. • A fast learner with a good sense of judgment and original thinking. Ability to thrive in ambiguity and adjust quickly to change. • A commercial mindset with experience building business cases from market research and analysis. • Excellent communication, presentation and analytical skills. • Customer service orientation and experience working in a client facing capacity.

Производственная компания, которая занимается сбором и переработкой лома цветных металлов, открывает позицию Коммерческий директор.   Главный вектор компании — в развитии циклической экономики, в разработке направлений утилизации и рециклинга. Цель компании — развитие экологической культуры через долгосрочное сотрудничество со всеми участниками цепочки промышленного производства.   Задачи:
Разработка стратегии и плана развития продаж
Формирование бюджета продаж и закупа
Командировки и встречи со стратегически важными клиентами
Реализация кадровой политики в коммерческом блоке (создание команды с «0»)   Требования:
Наличие опыта по выводу на рынок нового продукта
Наличие опыта работы или понимание деятельности тендеров
Навык аналитической деятельности   Условия:
Официальное трудоустройство, компенсация ГСМ, мобильной связи, корпоративного обучения.
Заработная плата состоит из оклада, KPI, премии. На период испытательного срока устанавливается фиксированный оклад — 120.000 р. Совокупный доход составит 300 000р.   Внимание! Для отклика на вакансию нужен VPN Внимание! Вакансия от рекрутингового агентства!

Edtech-company Algorithmics is looking for a country CEO (Co-Owner).   As a country CEO and Co-Owner you will build successful business with us and co-own your country’s branch: Find the product-market fit for Algorithmics in your country
Launch own schools (both offline and online) and engage new franchise partners
Hire and lead marketing, sales, operations, and localization teams   Priority countries: Asia: Indonesia, India, the Philippines, Vietnam, South Korea, Japan. etc.
LATAM: Brazil, Argentina, Mexico, etc.   Requirements: Experience in launching and promoting new products
Entrepreneurship experience or leading role in one of the well-performing companies.

Внимание! Вакансии нет на российских job ресурсах.   А leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry IQVIA is looking for a Senior Medical Director — Internal Medicine Europe.   The role: The Senior Medical Director provides medical and scientific support to clinical research programs, study teams, and investigators. The Senior Medical Director also provides medical leadership, review, and advice for potentially or actually awarded clinical research programs. He/she also may serve as a Medical Mentor to junior staff members. The Senior Medical Director may serve as lead on special projects or assignments for the Medical Department, as requested by the VP, Medical or designee. The Senior Medical Director role is a team member participant role and functions in a matrix and reports to project teams much like other members of project teams. The primary role of Senior Medical Director is to serve as Medical Monitor for studies conducted by IQVIA Biotech on behalf of sponsor companies. In the role of Medical Monitor, the Senior Medical Director provides medical oversight as the first line of support for clinical trials to which he/she is assigned as Medical Monitor. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as a medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators and study team members on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues.   Duties: Per sponsor request, reviews and provides input for protocol development; interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints; interacts in a team approach to develop statistical and data management sections of the protocol; reviews the final protocol for clinical, safety and efficacy variables
Functions as project team member
Provides project team with training on therapeutic indication and/or treatment modality
May provide study team with assistance in developing criteria for investigator site selection and networking for potential investigators for study participation, and aid in review and final selection
Participates in subject recruitment and retention activities which may include per sponsor request individual calls to key opinion leaders, investigators and site staff, and participation in teleconference and virtual presentations
Per sponsor request, presents protocol and/or safety reporting information at investigator meetings
Develops project medical monitoring plan
Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues
Provides medical input into the development of study protocols, training materials, informed consent, Investigator Drug Brochures, analysis plan designs, clinical study reports, regulatory approval submissions
Provides on call coverage for protocol queries and site support. Works with the IQVIA Biotech or vendor Safety Management Department to provide medical review and case assessment of SAEs/UADEs including review and edits of SAE narratives and safety queries, follow-up on outstanding safety queries, and interacting with sponsors and investigative sites to discuss safety issues as needed
Per sponsor request, reviews IND/SUSAR Safety Reports, updates to Investigator Brochures, and annual IND reports with sponsor data
In consultation with the sponsor, follows procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind)
Interacts with regulatory officials concerning safety and other study related issues, as requested. Provides medical review of eCRFs and edit check specifications for clinical accuracy
When indicated, provides Medical Data Review Plan as appendix to the Medical Monitoring Plan
Performs medical review of coded terms (e.g. adverse events, concomitant medications and medical history) for medical accuracy and consistency
Provides individual and aggregate review of clinical data as requested and specified in the Medical Data Review appendix
Reviews laboratory data as requested by sponsor and as specified in the MMP or Medical Data Review Appendix
Reviews data tables, listings, and figures as requested by sponsor
Reviews and/or writes portions of final clinical study report as requested by sponsor. Works with Business Development to actively solicit new business for IQVIA Biotech, including assistance with marketing presentations and proposal development
Interacts with clients regarding drug development programs, study design and protocol development
Reviews and provides medical and scientific input to new business proposals
Participates in feasibility discussions relating to specific project proposals
Supports business development activities with proposal development and sales presentations. Obtains literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
Assists with drafting of standard operating procedures and working practices regarding Medical Director activities
Participates in a variety of team quality improvement efforts as necessary
Performs other related duties as assigned or requested by the Vice President, Medical or designee   Skills: Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus
Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment
Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.   Внимание! Для отклика на вакансию нужен VPN

Внимание! Вакансии нет на российских job ресурсах.   А leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry IQVIA is seeking a Senior Clinical Project Management Director.   Job overview: Senior Clinical Project Management Directors are an integral part of project trial delivery liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The senior CPM Director is part of the core project team responsible for clinical delivery and oversight of complex, global full service, multi-regional studies or a program of studies to meet contractual requirements and in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The senior CPM Director focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers.   Essential functions: Contribute to the development of the project delivery strategy for RFPs. Participate in bid defense preparations. Lead bid defense presentations in partnership with business development for large, complex, multi-service, multi-region studies or programs. Understand project strategy and operationalise the agreed upon approach.
Oversee the development of integrated study management plans with the core project team.
Oversee the execution of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
Recognize systemic issues at the program or portfolio level and identify solutions with the project teams, recommend actions to improve efficiencies and oversee the implementation of best practices, address escalation items with the customer.;
Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
Oversee progress against contract and prepare/present project information proactively to all stakeholders internally and externally.
Responsible for the oversight and team management of large and complex studies or programs of studies.
Responsible for portfolio management with one customer or therapeutic area.
Manage strategic risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
Achieve project quality by identifying quality risks and issues, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.
Serve as primary project/program/portfolio contact with customer and own relationship with key customer contact(s), communicate/collaborate with IQVIA business development as necessary.;
Drive consistency of operational delivery across customer’s projects/programs/portfolio.
Build the cross-functional program/portfolio team and lead their efforts.
Responsible for ensuring the financial success of programs/portfolio.
Forecast and identify opportunities to accelerate activities to bring revenue forward.
Identify and communicate strategic lessons learned and best practices to promote continuous improvement.
Participate in, champion and adopt function and/or corporate initiatives, changes and/or special project assignments, act as a client liaison, departmental cross-functional liaison and/or change agent.   Qualifications: Bachelor’s Degree Life sciences or related field Req
Requires extensive knowledge of multiple job areas obtained through advanced education and experience.
Viewed as a leading expert within the field by peers.
Requires 15 years clinical research experience including 10 years of project management experience.
Equivalent combination of education, training and experience.
Knowledge of clinical trials — Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements, i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.;
Knowledge of clinical trials — Broad protocol knowledge, therapeutic knowledge desired.;
Knowledge of clinical trials — Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.
Communication — Strong written and verbal communication skills including good command of English language Strong presentation skills.
Problem solving — Strong problem solving skills.
Leadership — Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.;
Leadership — Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
Organisation — Planning, time management and prioritization skills.
Organisation — Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.;
Prioritisation — Ability to handle conflicting priorities.
Prioritisation — Ability to work strategically to realize project goals, identifying and developing positive and compelling visions for the successful delivery of the project.
Quality — Attention to detail and accuracy in work.
Quality — Results-oriented approach to work delivery and output Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.
IT skills — Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
Collaboration — Ability to establish and maintain effective working relationships with coworkers, managers and clients. Excellent customer management skills and demonstrated ability to understand customer needs Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.
Cross-collaboration — Ability to work across geographies displaying high awareness and understanding of cultural differences Good understanding of other IQVIA functions and their inter-relationship with Project Leadership.
Finances — Good understanding of project financials including experience managing, contractual obligations and implications.
IQVIA Core Competencies — Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).   Внимание! Для отклика на вакансию нужен VPN.