R&D Partners is seeking a Senior Clinical Project Manager to join their team. In this role, you will oversee clinical research studies, ensuring they are conducted efficiently, within budget, and in compliance with regulatory guidelines.
Responsibilities:
- Manage clinical research studies to meet timelines, budgets, and regulatory standards
- Act as the main point of contact for sponsors and lead study-related activities
- Oversee various clinical functions, such as data management, investigational supply, and pharmacovigilance
- Prepare and present study updates and reports to stakeholders
- Support and supervise clinical team members, including training and guidance
- Create and review essential study documents like protocols, budgets, and manuals
- Facilitate teamwork and communication to ensure project goals are met
- Monitor subject enrollment, retention, and compliance
- Assist with document management and prepare for audits or inspections
- Ensure adherence to industry regulations and company procedures
Requirements:
- Background in life sciences or a related field (or equivalent experience)
- Experience in clinical project management within the pharmaceutical, biotechnology, or CRO industry
- Strong organizational skills and attention to detail
- Ability to manage multiple tasks in a fast-paced environment
- Excellent problem-solving, leadership, and communication skills
- Proficiency in MS Office tools, especially Word and Excel
- Permanent authorization to work in the U.S