Clinical Research Coordinator- The Mindich Child Health and Development Institute
Mount Sinai Health System
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- Location
- United States
- Job type
- Full time
- Posted
- Oct 6
- 14 days ago
Career path
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About the company
Mount Sinai Health System
Hospital & health care · 10,001+ employees
What you'll do
- Conducts and assists with clinical research, including obtaining consent, screening and registering participants, administering questionnaires, and collecting and reviewing data.
- Maintains study documents and files, assists with grant and regulatory submissions, and may handle clinical specimens.
What you need
- Bachelors degree in science or related field preferred or a combination of relevant research experience and education.
- 0-2 years of research/human subjects experience.
- Education: a bachelor's degree
Key skills
Informed consentHuman subjects researchResearch techniquesInterview techniquesClinical research
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Read the full posting here
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and organizes study information. Assists in the preparation and submission of grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office).
Bachelors degree in science or related field preferred or a combination of relevant research experience and education.
0-2 years of research/human subjects experience.
Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff.
Assists in the activities related to clinical research including, but not limited to: obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering questionnaires and answering telephone calls.
Assists in the collection, analysis and review of experimental data for publication and presentation.
Maintains source documents and subject files in accordance with Mount Sinai policies and procedures. Ensures accurate, confidential and complete compilation of data.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Performs other related duties.