4 дня назад
Project Manager (Cardiac Safety)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Project Manager (Cardiac Safety) (Clinical Trials/Drug Development): Managing clinical study planning, execution, monitoring, and closeout with an accent on customer requirements, study documentation, financial oversight, and stakeholder coordination. Focus on identifying study risks, resolving client issues, tracking equipment and timelines, and supporting high-quality cardiac safety study outcomes.
Location: Remote in Costa Rica; willingness to travel up to approximately 20% is required.
Company
, part of Thermo Fisher Scientific, provides clinical trial technology and services to support better evidence and drug development.
What you will do
- Lead planning, setup, monitoring, and closeout for clinical studies.
- Translate customer requirements into actionable plans for internal teams.
- Maintain study documentation, reports, data archiving, and issue tracking.
- Coordinate equipment distribution and tracking for study execution.
- Monitor timelines, budgets, revenue forecasts, scope changes, and invoice reconciliation.
- Manage risks, client issues, stakeholder communications, negotiations, and study meetings.
Requirements
- Bachelor’s degree or equivalent practical experience in project management or a related field.
- 1–4 years of project management experience in the pharmaceutical, clinical, or related industry.
- Knowledge of the drug development lifecycle and clinical trial processes.
- Strong organizational, prioritization, communication, and problem-solving skills.
- Ability to communicate effectively in English.
- Proficiency in Microsoft Office, a valid passport, and willingness to travel up to approximately 20%.
Culture & Benefits
- Flexible work arrangements.
- Competitive compensation.
- Health and wellness programs.
- Paid time off and holidays.
- Cross-functional collaboration and opportunities to support clinical study teams.
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