Intern – Clinical Operations
About The Position
Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. We are seeking a highly motivated Intern to join our Clinical Operations group at Cytokinetics. Job Description: The intern will support clinical trial operations for the CY 1033 COMET study by working closely with study team members to assist with study-related activities, including documentation, coordination, and data support, while gaining hands-on experience in clinical research. The intern may also provide support across additional clinical trials as needed to ensure smooth study execution and compliance.
Requirements
- The position requires a motivated individual with the ability to work independently and in a team environment.
- Currently enrolled at an accredited college/university as a rising senior or higher.
- Effective oral and written communication skills.
- Able to communicate effectively with members of other departments and with study-site personnel (physicians, study coordinators, nurses, etc.) as needed.
- Ability to troubleshoot problems with team members
- Proficiency with computer applications such as Word, Excel, and PowerPoint and able to learn other applications with appropriate training.
- Significant attention to detail, time management, and organizational skills.
- When applying, please provide your spring break and summer availability.
Responsibilities
- Support day-to-day clinical trial activities for the CY 1033 COMET study under guidance of study team members
- Assist with preparation, review, and maintenance of study documentation (e.g., trial master file, study trackers, meeting minutes)
- Help coordinate study-related activities, including site communications, study meetings, and follow-ups
- Support data collection, entry, and quality checks in clinical trial systems
- Assist with tracking study milestones, timelines, and deliverables
- Support compliance with study protocols, GCP guidelines, and regulatory requirements
- Participate in study team meetings and contribute to action item follow-up
- Provide administrative and operational support to ensure smooth study execution
- Assist with audit or inspection readiness activities as needed
- Provide cross-study support for other clinical trials when required
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What This Job Offers
Career Level
Intern
Education Level
No Education Listed
Number of Employees
251-500 employees
