Clinical Project Coordinator

Benefits

Qualifications

• •Bachelor’s Degree in related field with a Minimum 3 years of experience in clinical research, biotech/pharma, or academic research environment
• •Experience with data interpretation, abstract/manuscript preparation, or project management tools
• •General knowledge and basic application of business concepts, procedures and practices
• •Minimal independent decision making
• •Strong organizational and communication skills with the ability to manage multiple tasks
• •2 more items(s)

Responsibilities

• •The Clinical Project Coordinator contributes to the coordination and execution of externally sponsored research projects
• •The role bridges scientific and operational functions, ensuring that project deliverables align with organizational objectives while maintaining compliance with internal standards and external regulations
• •Assist in planning, coordinating, and monitoring research project activities, including timelines, deliverables, and risk management
• •Support the preparation, review, and organization of scientific content such as study protocols, abstracts, presentations, and manuscripts
• •Facilitate communication across cross-functional teams (scientific, clinical, regulatory, and operational) to ensure smooth information flow
• •Contribute to data collection, interpretation, and internal reporting of research outcomes
• •Maintain project documentation, tracking tools, and support use of project management systems
• •Participate in special initiatives and process improvement activities
• •Independently manages own workload by balancing multiple tasks/projects, prioritizing work based on criticality and urgency, and completing takes on time
• •Will perform this job in a quality system environment
• •Failure to adequately perform tasks can result in noncompliance with government regulations
• •Learns to use professional concepts and company policies and procedures to solve routine problems
• •Works on problems of limited scope
• •10 more items(s)