Clinical Research Operations Associate
New
I
IndeedClinical Research
Bogota, Colombia; Brasilia, Brazil; Buenos Aires, Argentina; Cairo, Egypt; Mexico City, Mexico, Central Time Zone alignment requiredFull-TimeMiddle
Salary not disclosed
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Job Details
- Experience
- Minimum 5 years
- Required Skills
- Project ManagementMicrosoft Office Suite
Requirements
- Minimum 5 years of clinical research experience, with direct knowledge of clinical research coordinator duties, patient recruitment, and contracting.
- Experience with e-source design and implementation (CRIO, Clinical Conductor, RealTime strongly preferred).
- Strong understanding of clinical trial operations from startup through closeout.
- Demonstrated ability to manage projects independently and deliver results without extensive supervision.
- Excellent organizational, communication, and problem-solving skills.
- Adaptability to thrive in a fast-paced startup environment.
- Ability to work full-time, remote, aligned to Central Time Zone.
- Proficiency in Microsoft Office Suite and project management tools.
Responsibilities
- Act as the right hand to the VP of Operations, providing day-to-day operational support and workload relief.
- Manage and execute operational projects, ensuring timelines and deliverables are consistently met.
- Leverage expertise in clinical research operations to support patient recruitment, contracting, and study execution.
- Support the development and design of e-source templates and workflows.
- Provide oversight and input on contracts, budgets, and site-level processes.
- Serve as a subject matter expert across the clinical research lifecycle, including coordinator-level responsibilities.
- Anticipate needs and proactively resolve issues to keep projects moving forward.
- Develop documentation, SOPs, and best practices to support continuous improvement initiatives.
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