
51 - 200 employees
Founded 1996
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
Healthcare • Consulting • Logistics
ProTrials Research Inc. is a clinical research organization (CRO) headquartered in the United States, offering a wide range of services to the pharmaceutical, biotechnology, and medical device industries. The company provides quality-driven site management, clinical monitoring, project management, data management, and supportive clinical development services. With a focus on therapeutic areas such as oncology, ophthalmology, central nervous system, infectious diseases, women's health, and medical devices & diagnostics, ProTrials is dedicated to delivering high-quality clinical research. Their services include project management, clinical operations, quality assurance, medical and regulatory support, and they also act as a functional service provider, emphasizing virtual trials and remote monitoring capabilities.
đź•’ October 1
🇺🇸 United States – Remote
đź’µ $128k - $182k / year
⏰ Full Time
🟡 Mid-level
đźź Senior
🏥 Clinical Operations
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51 - 200 employees
Founded 1996
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
Healthcare • Consulting • Logistics
ProTrials Research Inc. is a clinical research organization (CRO) headquartered in the United States, offering a wide range of services to the pharmaceutical, biotechnology, and medical device industries. The company provides quality-driven site management, clinical monitoring, project management, data management, and supportive clinical development services. With a focus on therapeutic areas such as oncology, ophthalmology, central nervous system, infectious diseases, women's health, and medical devices & diagnostics, ProTrials is dedicated to delivering high-quality clinical research. Their services include project management, clinical operations, quality assurance, medical and regulatory support, and they also act as a functional service provider, emphasizing virtual trials and remote monitoring capabilities.
• Lead clinical study operations, including strategic and tactical planning, organization, and direction of study projects • Oversee clinical project timelines, reports, budgets, monitoring, site and vendor management, clinical supplies, and data collection • Facilitate communication between sponsors, study teams, and functional groups • Manage, motivate, and mentor study team members • Provide financial oversight of study budgets, including out-of-scope tracking • Collaborate with senior management on study updates, progress, resourcing, sponsor issues, and health status • Develop, maintain, and distribute project plans throughout the study lifecycle • Manage studies in compliance with GCP, SOPs, regulatory requirements, and project-specific plans • Assess resourcing and training needs and implement appropriate training plans • Delegate responsibilities and ensure team members have necessary tools and resources • Track study risks, escalate issues, and adjust timelines as needed • Oversee outside vendor activities and deliverables
• RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training and previous CRA experience • Outstanding interpersonal, oral, and written communication skills • Proven effectiveness as a team leader • Prior experience successfully managing multifaceted studies from inception through implementation and completion • Outstanding organizational and time management skills • Experience managing projects in a virtual environment • Demonstrated ability to lead by example and encourage team members to seek solutions independently • Proficiency in Microsoft Word, Excel, and PowerPoint required • Experience with MS Project and OneNote a plus
• Full medical, dental, and vision insurance options for you and your family • Flexible PTO • 401(k) plan with a company match • Support and opportunities for skills expansion and career advancement • Collaborative coworkers
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