Feasibility Manager evaluating clinical trial sites to advance pipeline and create strategic partnerships. Play a pivotal role in bringing clinical trials to life in Argentina.
About the role
- Clinical Research Project Coordinator overseeing administrative aspects of human subjects research projects. Implementing daily operations and ensuring compliance with research protocols and budgets.
Responsibilities
- Provides oversight and support in the research and non-clinical administrative aspects of projects involving human subjects.
- Implements and oversees the daily operations of the study, including monitoring participant recruitment and implementing protocols.
- Manages research data and samples, and supervises staff.
- Assists with administrative functions including IRB compliance, maintaining supplies, writing proposals, and ensuring compliance with grant criteria.
- Aids in preparing and reviewing submissions to sponsors, including budgeting, and maintaining project budgets.
Requirements
- Bachelor's Degree Required
- Minimum 3 to 5 Years of Experience
- CCRP, CCRA, or ACRP-CP preferred
- Excellent communication skills and analytic abilities
- Basic computer skills, e.g. familiarity with Microsoft software, completing spreadsheet/data entry
- Ability to work with diverse populations and support an inclusive, culturally responsive environment.
Benefits
- Health insurance
- Retirement plans
- Paid time off
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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