DescriptionThe Milton and Carroll Petrie Department of Urology has long been a leader in clinical practice education and research. Faculty in our Department which is housed within the Icahn School of Medicine at Mount Sinai perform complex procedures using robotics laparoscopy and endoscopy all as a part of our minimally invasive urologic surgery program. We remain equally committed to engaging in breakthrough research while training the next generation of leaders in the field.
Under minimal supervision the Clinical Research Coordinator II coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g. Institutional Review Board Grants and Contracts Office).
Responsibilities- Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
- Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
- Prepares and ensures grant applications IRB/GCO documents are submitted.
- Ensures accurate and complete compilation of subject data through chart reviews.
- Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions protocol amendments and renewals of ongoing clinical trials.
- Obtains informed consent under supervision of the Principal Investigator Clinical Research Manager or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects and for studies involving genetic tests.
- Independently obtains informed consent for other clinical studies.
- Mentors Clinical Research Coordinators in training.
- Performs other related duties.
Qualifications- Bachelors degree in sciences or related field.
- 2 years of clinical research
Required Experience:
IC
DescriptionThe Milton and Carroll Petrie Department of Urology has long been a leader in clinical practice education and research. Faculty in our Department which is housed within the Icahn School of Medicine at Mount Sinai perform complex procedures using robotics laparoscopy and endoscopy all as a...
DescriptionThe Milton and Carroll Petrie Department of Urology has long been a leader in clinical practice education and research. Faculty in our Department which is housed within the Icahn School of Medicine at Mount Sinai perform complex procedures using robotics laparoscopy and endoscopy all as a part of our minimally invasive urologic surgery program. We remain equally committed to engaging in breakthrough research while training the next generation of leaders in the field.
Under minimal supervision the Clinical Research Coordinator II coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g. Institutional Review Board Grants and Contracts Office).
Responsibilities- Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
- Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
- Prepares and ensures grant applications IRB/GCO documents are submitted.
- Ensures accurate and complete compilation of subject data through chart reviews.
- Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions protocol amendments and renewals of ongoing clinical trials.
- Obtains informed consent under supervision of the Principal Investigator Clinical Research Manager or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects and for studies involving genetic tests.
- Independently obtains informed consent for other clinical studies.
- Mentors Clinical Research Coordinators in training.
- Performs other related duties.
Qualifications- Bachelors degree in sciences or related field.
- 2 years of clinical research
Required Experience:
IC
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