Full-Time Clinical Trial Project Manager
Paradigm Health is hiring a remote Full-Time Clinical Trial Project Manager. The career level for this job opening is Experienced and is accepting USA based applicants remotely. Read complete job description before applying.
Paradigm Health
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Paradigm is rebuilding the clinical research ecosystem by enabling equitable access to trials for all patients. Our platform enhances trial efficiency and reduces the barriers to participation for healthcare providers.
Job Overview:
We are seeking an experienced Clinical Trial Project Manager to join our Operations team.
Responsibilities:
- Manage and oversee contracted clinical trials from inception to completion.
- Ensure all projects are completed on time, within budget, and compliant with regulations.
- Coordinate with cross-functional teams and stakeholders (study sponsors, CROs).
- Establish standard project management templates and processes.
- Track project progress and KPIs, identify blockers, and coordinate resources.
- Communicate effectively with internal and external stakeholders.
- Coordinate Execution of Sponsored Trials: Plan, initiate, lead, and manage clinical trials. Develop comprehensive project plans.
- Regulatory Compliance: Ensure all trials comply with regulations, GCP guidelines, and SOPs.
- Communication: Serve as a primary point of contact between sponsors and internal teams.
- Support of Sales: Develop client relationships, generate new business.
- Operational Excellence: Establish best practices for project management, quality assurance.
Qualifications:
- BA/BS degree or equivalent work experience.
- 3+ years client-facing experience.
- Experience managing relationships with enterprise clients.
- CRO/Pharmaceutical experience preferred.
- Strong knowledge of GCP/ICH guidelines.
- Strong project and program management skills.
- Proactive problem-solving skills.
- Excellent communication skills across various teams.
- Comfort with data and reporting systems.
- Understanding of digital health technologies.
- Strict confidentiality.
- Previous clinical trial experience a plus.