Project Manager – Cardiac Safety

🔥 0 minutes ago

🇨🇷 Costa Rica – Remote

⏰ Full Time

🟢 Junior

👷‍♀️ Project Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 Private Equity Round on 2019-10

Healthcare • Consulting • Logistics

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• Lead the planning, setup, monitoring, and closeout phases of clinical study management, ensuring delivery of high-quality services • Gather and translate customer requirements into actionable plans for internal teams • Develop and maintain study documentation, reports, and data archiving processes • Coordinate equipment distribution and tracking to support study execution • Monitor study timelines and manage financial components, including budgets, revenue forecasting, scope changes, and invoice reconciliation • Identify study risks, propose mitigation strategies, and escalate issues as appropriate • Manage internal and external stakeholder communications, negotiations, and relationships to ensure alignment and collaboration • Promote a positive team environment through effective communication and resource coordination • Apply structured problem-solving approaches to resolve client issues and maintain issue tracking for timely resolution • Represent study services in client meetings, including investigator and site initiation meetings, as needed • Support onboarding and training of new Project Management team members

🎯 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, time management, and prioritization skills • Excellent interpersonal and communication skills, with the ability to communicate effectively in English • Proficiency in Microsoft Office applications • Detail-oriented with demonstrated responsiveness and accountability • Ability to manage multiple priorities in a fast-paced environment • Valid passport and willingness to travel up to approximately 20%

🏖️ Benefits

• Competitive compensation • Health and wellness programs • Flexible work arrangements • Paid time off and holidays