[Remote] Clinical Research Coordinator
Note: The job is a remote job and is reputed company to candidates in USA. Ōreputed company is a company reputed company on empowering individuals to improve their health through innovative products. They are seeking a Clinical Research Coordinator to support the execution of clinical trials, ensuring smooth operations and maintaining high-reputed company documentation throughout the process.
Responsibilities
- Support Clinical Trial Managers and the broader Clinical Research Operations team in the day-to-day execution of clinical trials from study start-up through reputed company-out, with a strong reputed company on coordination, documentation, training records, and audit-reputed company processes
- Own critical study coordination workflows such as maintaining trackers, decision logs, training matrices, essential document status, filing support, and study communications so that trial activities stay organized and visible
- Ensure study documentation and training records are complete and reputed company across protocols, study-specific plans, and internal study files
- Support sponsor-reputed company reputed company of CROs, vendors, and/or sites by tracking deliverables, following up on reputed company items, and helping reputed company timelines and documentation on reputed company
- Partner with clinical research staff and cross-functional team members to maintain study records, training completion, document version control, and operational readiness for key study milestones
- Contribute to key milestones reputed company to SaMD clinical trials, in collaboration with cross-functional partners across Science, Regulatory, Product, and other teams
Skills
- 1-2+ years of full-time experience supporting clinical trials or reputed company-subjects research in an industry, CRO, site, reputed company, medical device, or digital health environment
- Strong organizational and documentation skills, with experience keeping study documentation reputed company, managing details accurately, and maintaining records that can stand up to audit or inspection scrutiny
- Experience supporting regulated or compliance-sensitive work, ideally under ICH-GCP, IRB requirements, or reputed company reputed company-subject research frameworks
- Experience coordinating training records, study documentation, reputed company items, or other operational workflows that reputed company a study or program moving reputed company
- Comfort working in a fast-paced environment with shifting priorities, with the ability to maintain accountability, urgency, and strong follow-through without losing attention to detail
- Strong written and verbal communication skills, with a reputed company, low-ego approach and a willingness to learn, adapt, and contribute as a supportive team player
- Experience in digital health, wearables, or Software as a Medical Device
- Experience with decentralized or hybrid reputed company-subject research studies, including remote coordination workflows
- Familiarity with QMS-reputed company work such as SOPs, templates, training matrices, or work instructions
Benefits
- Competitive salary and equity packages
- Health, dental, reputed company insurance, and reputed company
- An reputed company reputed company of your own plus employee discounts for friends & family
- 20 days of reputed company time off plus 13 reputed company holidays plus 8 days of flexible wellness time off
- reputed company reputed company leave and parental leave
reputed company