Clinical Research Coordinator I-Pathology, Molecular and Cell Based Medicine
Mount Sinai Health System
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- Location
- United States
- Job type
- Full time
- Posted
- Oct 27
- 1 day ago
Career path
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About the company
Mount Sinai Health System
Hospital & health care · 10,001+ employees
What you'll do
- Collects and records study data and inputs information into database
- Obtains informed consent and educates participants regarding study requirements
- Assists with answering phone calls, screening participants, registering subjects, and questionnaires
- Assists in preparing grant applications, IRB/GCO submissions, and filings
- Maintains source documents and subject files and compiles subject data through chart reviews
- Secures, delivers, and ships clinical specimens as required by the protocol
- Prepares for monitoring visits
- Prepares samples using standard immunological techniques and maintains experiment data
What you need
- Bachelors or Masters degree in Science or closely related field.
- No experience required. One year of research experience preferred.
- 1-2 years of previous clinical research experience
- Excellent written and oral communication skills
- Exceptional attention to detail
- Education: a bachelor's degree or a postgraduate degree
Key skills
Exceptional attention to detailstandard immunological techniques
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Read the full posting here
The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Prepares tissue samples for analyses. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).
Bachelors or Masters degree in Science or closely related field.
No experience required. One year of research experience preferred.
Preferred
1-2 years of previous clinical research experience
Excellent written and oral communication skills
Exceptional attention to detail
Collects and records study data. Inputs all information into database.
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
Secures, delivers and ships clinical specimens as required by the protocol.
Prepares for monitoring visits.
Performs other related duties, including sample preparation using standard immunological techniques; maintains data/results of all experiments.