от компании (организации): ООО БОСТОНДЖИН в городе (населённом пункте): Москва, Россия
в отрасли экономики "Наука, образование" → "Биотехнологии"
с заработной платой: по договоренности
Вакансия № 22712845 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Суббота, 31 августа 2024 года.
Дата обновления вакансии № 22712845 на сайте Работа в Москве и Московской области (МО, Подмосковье): Суббота, 28 сентября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 22712845 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
1–3 года
Тип занятости:
полная занятость
График работы:
гибкий график
Дополнительные сведения о вакансии: Clinical report coordinator
BostonGene Corporation is pioneering the use of biomedical software for advanced patient analysis and personalized therapy decision-making in the fight against cancer. Our unique solution continuously aggregates the latest cancer research and clinical information from around the world. BostonGene’s unique solution performs sophisticated analytics to aid clinicians in their evaluation of viable treatment options for each patient’s genetics, tumor and tumor microenvironment, clinical characteristics, and disease profile. BostonGene’s mission is to enable physicians to provide every patient with the highest probability of survival through optimal cancer treatments using advanced, personalized therapies via sophisticated analytics and integration of scientific and clinical knowledge.
Responsibilities:
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Operational support of report generation process and involved teams (MSLs, lab, bioinformatics, analytics);
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Support new case set up and case document management;
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Manage data and timeline of the entire life-cycle of all reports assigned;
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Juggle multiple reports and priorities simultaneously in a fast-paced environment;
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Liaise with sales staff to clarify report parameters;
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Communicate any issues/problems/caveats or additional information to sales and R&D teams;
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Commit to continuous quality improvement of existing workflows, processes, and documentation.
Preferred Qualifications
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1+ years of academic or professional experience in molecular biology, clinical oncology, or fundamental medicine;
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Master degree or equivalent in medicine, biology, bioinformatics or other relevant fields;
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Experience in scientific data management in various phases of project design and analysis;
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Track record of applying attention to detail and of meeting short- and long-term deadlines;
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Self-starter; motivated, and goal-oriented; demonstrates the ability to work independently and in a team environment;
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Detail-oriented and highly organized; methodical approach to process-oriented tasks;
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Ability to effectively prioritize and manage multiple projects simultaneously; works well under pressure and able to meet tight deadlines;
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Performs well in a fast-paced fluid environment; adapts quickly to change;
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Effective communicator (verbal and written); ability to professionally communicate at all levels both internally and externally with project stakeholders.
We offer:
- Full-time position, permanent contract, flexible working hours;
- Versatile professional environment: bioinformatics, biologists, physicians, and software developers who united to save people’s lives;
- The office is located in Moscow, Paveletskaya metro station;
- Competitive salary and medical insurance.
Откликнуться на эту вакансию: Clinical report coordinator
Предыдущая вакансия:
Вакансия № 22712840 на должность Ведущий юрисконсульт от компании ООО НЭМЗ в городе (населенном пункте) Красногорск