Clinical Research Coordinator II- Pulmonary

Mount Sinai; United States; On-site; USD 55,000 - 85,000; Full time

Job summary

Mount Sinai seeks a Clinical Research Coordinator to coordinate the clinical assessments of study subjects and support data analysis and grant-related submissions. The role involves assisting with IRB submissions and ensuring comprehensive documentation.

Under supervision, you will screen and evaluate participants, manage consent processes, and collaborate with PI and regulatory staff on protocol amendments and ongoing trials. Training and mentorship are available.

Qualifications

• Bachelor's degree in sciences or related field.
• Minimum 2 years of clinical research experience.

Responsibilities

• Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
• Analyzes moderately complex clinical research data and assists in interpretation of results.
• Prepares and ensures grant applications and associated documents are submitted (IRB/GCO).
• Ensures accurate compilation of subject data through chart reviews.
• Assists PI and regulatory staff with protocol submissions, amendments, and renewals.
• Obtains informed consent under supervision and independently for studies.
• Mentors Clinical Research Coordinators in training.
• Performs other related duties.

Skills

Clinical research coordination

Data analysis

Grant preparation

Education

Bachelor's degree

Tools

IRB submissions

Job description

Under minimal supervision, 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).

• 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.

• Bachelors degree in sciences or related field.
• 2 years of clinical research