Mount Sinai Medical Center New York , NY 10007
Posted 4 days ago
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). Duties and Responsibilities: 1.
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data. 2. Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects. 3. Prepares and ensures grant applications, IRB/GCO documents are submitted. 4.
Ensures accurate and complete compilation of subject data through chart reviews. 5. Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials. 6. 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. 7.
Independently obtains informed consent for other clinical studies. 8. Mentors Clinical Research Coordinators in training. 9. Performs other related duties.
Job Qualifications Education: Bachelor's degree in sciences or related field. Experience: 2 years of clinical research Excellent verbal, written & interpersonal skills.
Knowledge of standard concepts, practices and procedures in directly related field. Exceptional attention to detail and accurac Responsibilities 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). Duties and Responsibilities: 1.
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data. 2. Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects. 3. Prepares and ensures grant applications, IRB/GCO documents are submitted. 4.
Ensures accurate and complete compilation of subject data through chart reviews. 5. Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials. 6. 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. 7.
Independently obtains informed consent for other clinical studies. 8. Mentors Clinical Research Coordinators in training. 9. Performs other related duties.
Job Qualifications Education: Bachelor's degree in sciences or related field. Experience: 2 years of clinical research Excellent verbal, written & interpersonal skills.
Knowledge of standard concepts, practices and procedures in directly related field. Exceptional attention to detail and accurac Qualifications Compensation Statement The Mount Sinai Health System (MSHS) provides a salary range to comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for this role is $58,661.00 - $74,250.00 Annually.
Actual salaries depend on a variety of factors, including experience, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. Non-Bargaining Unit, BIJ - Medicine Admin.
Compensation Statement The Mount Sinai Health System (MSHS) provides a salary range to comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for this role is $58,661.00 - $74,250.00 Annually.
Actual salaries depend on a variety of factors, including experience, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. Non-Bargaining Unit, BIJ - Medicine Admin.
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). Duties and Responsibilities: 1.
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data. 2. Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects. 3. Prepares and ensures grant applications, IRB/GCO documents are submitted. 4.
Ensures accurate and complete compilation of subject data through chart reviews. 5. Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials. 6. 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. 7.
Independently obtains informed consent for other clinical studies. 8. Mentors Clinical Research Coordinators in training. 9. Performs other related duties.
Job Qualifications Education: Bachelor's degree in sciences or related field. Experience: 2 years of clinical research Excellent verbal, written & interpersonal skills.
Knowledge of standard concepts, practices and procedures in directly related field. Exceptional attention to detail and accurac
Mount Sinai Medical Center