Clinical Project Manager
New
A
AlimentivClinical research
Philadelphia, Pennsylvania; Cincinatti, Ohio; Houston, Texas; Dallas, Texas; Toronto, Ontario; Vancouver, British Columbia; Montreal, Quebec; Raleigh-Durham, North CarolinaFull-TimeMiddle
Salary$95,500 - $159,000 a year
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Job Details
- Languages
- Fluency in English, including reading, writing, and speaking.
- Experience
- 1–3 years of experience in clinical study management
- Required Skills
- Project ManagementBudget management
Requirements
- Hold a bachelor's degree in a relevant field, preferably Health Sciences, Clinical Research, or a related discipline.
- Have 1–3 years of experience in clinical study management, including exposure to clinical research project coordination and execution.
- Demonstrate a strong understanding of clinical research processes, regulatory requirements, quality standards, and study documentation practices.
- Bring project management and organizational skills to coordinate multiple tasks, track deliverables, and meet deadlines.
- Communicate effectively in writing and verbally with sponsors, clients, investigators, and cross-functional teams.
- Build collaborative working relationships and coordinate interdisciplinary project activities.
- Maintain accuracy, compliance, attention to detail, and high-quality project outcomes.
- Use problem-solving skills to identify and address project challenges proactively.
- Demonstrate self-motivation, results orientation, and commitment to continuous learning and adapting to evolving requirements.
- Be fluent in English, including reading, writing, and speaking.
- Work effectively in a home-based environment and travel occasionally as required.
Responsibilities
- Plan, execute, monitor, and complete assigned clinical research projects, delivering project objectives and deliverables.
- Coordinate cross-functional project teams to meet applicable regulations, industry guidelines, corporate policies, and quality standards.
- Oversee project operations, budgets, regulatory requirements, and patient safety throughout the project life cycle.
- Manage the development, maintenance, and disposal of study documents, data, equipment, and tools, including protocols, SOPs, informed consent forms, and CRFs.
- Assign and track interdisciplinary activities such as site monitoring, database development, data collection, adverse event management, statistical analysis, and clinical study reporting.
- Serve as the primary contact for sponsors and clients, managing expectations and resolving project issues.
- Organize project meetings, prepare investigator updates, and report progress and status to stakeholders.
- Support site and patient recruitment, stakeholder training, and study-related communication materials.
- Participate in regulatory submissions, audits, and third-party vendor selection.
- Monitor team performance, project milestones, and deliverable quality against sponsor expectations, project requirements, and regulatory standards.
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