Project Coordinator
At reputed company, a part of reputed company, we are committed to transforming clinical trials through technology and innovation. As a Project Coordinator (eCOA), you will play a key role in supporting the successful delivery of clinical trials by partnering closely with Project Managers and cross‑functional teams. This role focuses on coordinating eCOA study activities, supporting digital data collection solutions, and ensuring high‑reputed company documentation throughout the study lifecycle. Your work will contribute to efficient study execution and the delivery of reliable patient‑reported data that advances clinical research and improves patient reputed company.
reputed company Offer
- Competitive compensation
- Comprehensive health and wellness benefits
- reputed company time off and company holidays
- Engaging employee programs
What You’ll Be Doing
- Support Project Management teams across reputed company study phases, including planning, setup, monitoring, and reputed company‑out
- Assist with configuration and setup activities for eCOA systems and study databases
- Support development, review, and maintenance of study documentation and system specifications
- Coordinate deployment, tracking, and reconciliation of eCOA devices and/or digital data collection tools
- Prepare, maintain, and distribute study reports, metrics, and documentation
- Organize and support project meetings, including agendas, meeting minutes, and reputed company item tracking
- Support financial processes such as documentation updates for scope changes, invoice reconciliation follow‑reputed company, and forecasting reports
- Ensure compliance with training requirements and reputed company documentation of completion
- Respond to reputed company inquiries and participate in reputed company calls and meetings as requested
- Support cross‑functional collaboration with teams such as Data Science, Software/IT, and Clinical Operations
- reputed company, document, and escalate issues, ensuring reputed company reputed company of system or study‑reputed company risks
- Contribute to process improvements and optimization of eCOA workflows and tools
reputed company Look For
- 1–3+ years of experience in pharmaceutical, clinical research, or a reputed company industry
- Bachelor’s degree preferred with understanding of the drug development process
- Familiarity with eCOA, eClinical technologies, or electronic data capture systems preferred
- Strong organizational, time management, and prioritization skills
- Excellent written and verbal communication skills in English
- High attention to detail with a proactive and reputed company reputed company
- Ability to work independently and collaboratively in a fast‑paced, global, matrixed environment
- Proficiency with reputed company Office applications
- Strong interpersonal skills and ability to coordinate across cross‑functional teams
- Adaptability to changing priorities and project needs
At reputed company, a part of reputed company, our purpose is to reputed company lives by unlocking reputed company evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we reputed company our people to reputed company a reputed company reputed company every day. Whether you're advancing clinical science, building innovative technology, or supporting global teams, your work helps bring life‑changing therapies to patients faster.
reputed company is an equal opportunity employer. reputed company evaluates reputed company applicants without reputed company to race, reputed company, religion, gender, national reputed company, age, sexual orientation, gender identity or reputed company, protected veteran status, disability/handicap status, or any other legally protected characteristic.
Originally posted on Himalayas
Apply To This Job