Задачи:
Требования:
— Девушки и женщины в возрасте от 22 до 30 лет
— Наличие опыта работы
— Уверенное владение компьютером
— Знание русского языка
— Ответственность, вежливость и доброжелательность
— Умение работать в команде
Условия:
— Обед за счёт клиники
— График работы: понедельник–пятница с 09:00 до 18:00, суббота с 09:00 до 13:00
— Зарплата договорная
Задачи:
— Работа врачом-педиатром в ночную смену в клинике Hi-tech Laboratories.
Условия:
— Зарплата договорная.
— Работа в офисе по адресу: ул. Хусейна Байкары, Бектемирский район, Ташкент.
Требования:
— Обязательно наличие опыта работы с аппаратом EEG.
Условия:
— График работы: посменный, дневная смена.
— Время работы: с 16:30 до 22:00.
— Работа в вечернюю смену.
Зарплата обсуждается индивидуально.
ОфисТашкент
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Задачи:
— Подготовка стоматологического кабинета к приёму пациентов.
— Подготовка необходимых инструментов, материалов и оборудования.
— Ассистирование врачу-стоматологу во время приёма (работа «в четыре руки»).
— Ведение медицинской документации и заполнение журналов.
— Соблюдение санитарно-эпидемиологических норм и поддержание порядка в кабинете.
Требования:
— Среднее медицинское образование (специальность «Сестринское дело»).
— Опыт работы ассистентом стоматолога приветствуется, но не обязателен.
— Ответственность, аккуратность и внимательность к деталям.
— Доброжелательность, эмпатия и умение находить общий язык с пациентами.
— Желание обучаться, развиваться и работать в команде.
Условия:
— Прозрачная заработная плата от 5 000 ₽ за смену.
— Официальное трудоустройство по ТК РФ с выплатой заработной платы два раза в месяц.
— Гибкий сменный график: от 2–3 дней в неделю.
— Время работы с 9:30 до 20:30.
— Удобное расположение в Москве, м. Автозаводская / м. ЗИЛ.
— Помощь в прохождении необходимой аккредитации за счёт клиники.
— Обучение стандартам работы и внутренним протоколам.
— Стажировка для кандидатов без опыта: 2–4 смены.
Задачи:
— ассистирование врачу-стоматологу
— контроль стерильности пакетов
— работа с клкт
— уборка кабинета в процессе работы и после окончания смены
— отслеживание достаточности медицинских препаратов, соблюдения условий хранения и сроков годности лекарственных препаратов
— ведение журнала учета стерилизации, замены антисептических растворов
Требования:
— образование: среднее профессиональное
— специальность: «Сестринское дело»
— опыт работы по профессии минимум 1 год
Условия:
— оформление по ТК РФ
— график и зарплата обсуждаются
Задачи:
— Амбулаторный прием учащихся и ведение медицинской документации, включая работу в медицинской информационной системе (МИС);
— Выполнение назначений врача, контроль приема терапии и соблюдения рекомендаций;
— Проведение профилактических мероприятий;
— Санитарно-гигиенический контроль;
— Взаимодействие и коммуникация с родителями.
Требования:
— Среднее медицинское образование с действующим сертификатом или аккредитацией по сестринскому делу в педиатрии;
— Уверенное владение ПК и знание основных программ;
— Готовность работать на основном месте с полной занятостью и умение работать в команде.
Условия:
— Сменный график работы: смены по 12 часов или суточные по 24 часа с разными ставками;
— Оклад 100 000 рублей на руки;
— Трудоустройство по Трудовому кодексу РФ;
— Хороший социальный пакет.
Location: Brooklyn, United States; Staten Island, United States
Workplace: on-site
MUST HAVE PRIOR GASTROENTEROLOGY EXPERIENCE
Schedule:
Monday–Friday, 9:00 a.m.–5:00 p.m.
Excellent work-life balance: This is a fully office-based position with no hospital call, evenings, weekends, or holiday shifts.
A well-established gastroenterology practice is seeking an experienced Physician Assistant to join its outpatient team.
The ideal candidate will have direct GI experience in an outpatient practice or clinic setting. Candidates with hospital experience may also be considered if their background includes substantial outpatient GI clinic work.
Responsibilities
Evaluate and manage patients with gastrointestinal conditions
Conduct patient consultations, examinations, and follow-up visits
Develop treatment plans in collaboration with physicians
Review laboratory results, imaging, and other diagnostic information
Educate patients about their conditions and treatment plans
Maintain accurate and timely clinical documentation
Licensed Physician Assistant in New York State
Previous gastroenterology experience required
Outpatient or GI clinic experience required
Spanish-language skills are a plus
Strong clinical judgment and communication skills
Ability to work effectively within a collaborative practice
ОфисBrooklyn, United States; Staten Island, United States
Location: Staten Island, United States; Brooklyn, United States
Workplace: on-site
MUST HAVE PRIOR GASTROENTEROLOGY EXPERIENCE
Schedule:
Monday–Friday, 9:00 a.m.–5:00 p.m.
Excellent work-life balance: This is a fully office-based position with no hospital call, evenings, weekends, or holiday shifts.
A well-established gastroenterology practice is seeking an experienced Nurse Practitioner to join its outpatient team.
The ideal candidate will have direct GI experience in an outpatient practice or clinic setting. Candidates with hospital experience may also be considered if their background includes substantial outpatient GI clinic work.
Responsibilities
Evaluate and manage patients with gastrointestinal conditions
Conduct patient consultations, examinations, and follow-up visits
Develop treatment plans in collaboration with physicians
Review laboratory results, imaging, and other diagnostic information
Educate patients about their conditions and treatment plans
Maintain accurate and timely clinical documentation
Licensed Nurse Practitioner in New York State
Previous gastroenterology experience required
Outpatient or GI clinic experience required
Spanish-language skills are a plus
Strong clinical judgment and communication skills
Ability to work effectively within a collaborative practice
ОфисStaten Island, United States; Brooklyn, United States
Location: Brooklyn, United States; Staten Island, United States
Workplace: on-site
MUST HAVE PRIOR GASTROENTEROLOGY EXPERIENCE
Schedule:
Monday–Friday, 9:00 a.m.–5:00 p.m.
Excellent work-life balance: This is a fully office-based position with no hospital call, evenings, weekends, or holiday shifts.
Open to New Graduates and Experienced Professionals
At Resourceful Talent Group, we’re passionate about helping others succeed. Our mission is to find the perfect fit for clients and candidates every single time. No matter how unique or tough the task may be, we pair quality talent with the right team, and we do it with speed.
We're currently recruiting for a
Gastroenterologist
for our client with a Private Practice in the New York City Metropolitan Area.
Job Highlights:
Client: Private Practice with locations across NYC
Salary Guarantee: $450K + INCREDIBLE INCENTIVES!!!
Incentive of 60% GI / 40% Practice - If GI generates $1M then compensation for GI is $600K - Average earnings for GI at this practice!!
Variety of locations in quality areas across NYC, and a growing practice with an excellent reputation
Tight-knit practice with over 6 GI’s and operating for 10+ years. Significant financial opportunities!
Signing bonus upon signing and start!
New York City Highlights:
Top Medical Centers: Prestigious hospitals, research facilities offer cutting-edge opportunities.
Diverse Patient Mix: Wide range of cases, cultural experiences enhance practice.
Networking Hub: Conferences, institutions foster collaboration, career advancement opportunities.
Urban Lifestyle Benefits: Access to amenities, entertainment, enriching work-life balance.
Emerging Healthcare Landscape: Growing medical centers, community-oriented care opportunities.
* Doctor of Medicine (MD) or Doctor of Osteopathy (DO)
* Active licensure to practice medicine in the state of New York
* Board certification or eligibility for certification in Gastroenterology
ОфисBrooklyn, United States; Staten Island, United States
Location: Boston, MA
Workplace: OnSite
At WHOOP, we're on a mission to unlock human performance and healthspan. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives.
As a Temporary Clinical Research Associate, you will provide monitoring and clinical operations support across WHOOP’s portfolio of clinical research studies. You will support assigned studies at various stages of the clinical lifecycle, including startup, active study conduct, monitoring, and closeout.
You will conduct monitoring activities, review study documentation, support Trial Master File quality, track study issues, and help ensure that studies are conducted in accordance with approved protocols, Good Clinical Practice, applicable regulations, and WHOOP procedures.
This role requires a detail-oriented and collaborative CRA who can independently manage assigned monitoring activities, communicate effectively with research sites and internal teams, and escalate risks or compliance concerns appropriately. Depending on study timelines and business needs, you may support one or more studies during the contract period.
This is a 6 month, temporary position with an hourly pay rate of $45/hr.
RESPONSIBILITIES:
- Conduct remote and onsite monitoring activities for assigned studies, including Site Initiation Visits, Interim Monitoring Visits, Closeout Visits, and other study-specific visits.
- Perform monitoring activities in accordance with approved protocols, monitoring plans, Good Clinical Practice, applicable regulations, and WHOOP procedures.
- Review informed consent documentation, participant eligibility, source documentation, case report forms, protocol adherence, safety documentation, and study data for accuracy and completeness.
- Prepare accurate and timely monitoring visit reports, follow-up communications, action-item trackers, and study status updates.
- Identify, document, track, and escalate protocol deviations, data quality concerns, safety issues, compliance risks, and operational challenges.
- Support site readiness activities, including review of essential documents, training completion, systems access, and operational preparedness.
- Assist with site and study team training on protocols, study procedures, documentation requirements, and clinical systems.
- Create and maintain assigned study logs, trackers, monitoring templates, and clinical operations documentation.
- Collaborate with Clinical Operations, Clinical Science, Clinical Research Coordinators, Data Management, Regulatory, Quality, investigators, research sites, and external vendors.
- Support study closeout activities, including document reconciliation, action-item resolution, final monitoring activities, and Trial Master File completion.
QUALIFICATIONS
- Bachelor’s degree in life sciences, nursing, public health, clinical research, or a related field, or equivalent relevant experience.
- 3+ years of experience in clinical research, including at least 1 year performing clinical monitoring or CRA responsibilities.
- Strong attention to detail and the ability to identify and clearly document study risks, compliance concerns, and data quality issues.
- Strong written communication skills, including the ability to prepare clear monitoring reports and site follow-up correspondence.
DESIRED:
- Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies.
- Familiarity with ISO 14155 or clinical research involving medical devices.
- Experience working in a sponsor, CRO, or research-site environment.
- Experience supporting studies related to cardiovascular health, women’s health, sleep, metabolic health, or digital biomarkers.