Job Summary
The Clinical Research Associate I plays a vital role in overseeing various components of clinical research trials. This position is crucial for ensuring the effective management of the entire clinical study life cycle.
Responsibilities
- Monitor and manage all facets of clinical research trials.
- Oversee the implementation and adherence to research protocols and guidelines.
- Facilitate the development of essential documents such as informed consent templates and investigator brochures.
- Ensure compliance with monitoring guidelines and statements of work.
- Coordinate with laboratory and clinical staff to support research objectives.
Qualifications
- Relevant experience or educational background in clinical research.
- Strong understanding of clinical trial protocols and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a team-oriented environment.
- Detail-oriented with a commitment to maintaining high standards in research practices.
Icahn School of Medicine at Mount Sinai provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
