Support the successful execution of clinical research studies from start to finish, involving participant recruitment, data collection, sample processing, and documentation.
Responsibilities
Conduct study activities in compliance with GCP, SOPs, and protocols
Monitor participant safety
Perform scheduled visits and assessments (e.g., vitals, ECGs)
Support recruitment efforts and screen participants
Obtain informed consent and maintain accurate documentation
Requirements
Degree in a health, science, or research-related field
Equivalent hands-on experience in a healthcare or clinical setting
Oversee and conduct clinical research of consumer products involving healthy paid volunteers, ensuring compliance with SOPs, good clinical practice, and FDA regulations.
Compensation
Salary: $90,000 - $120,000 USD
Responsibilities
Develop research studies and protocols
Collect and review data, prepare progress reports
Analyze results and write summaries
Develop, maintain and review SOPs
Conduct and supervise studies per protocol
Requirements
PhD
MD
DO
post-graduate degree in Science, Medicine, or Engineering
Assist in the daily activities of clinical research studies, obtain informed consent, collect and maintain study data, prepare grant applications, and support research operations.
Compensation
The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $58661 - $73530 Annually.
Responsibilities
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 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
The Ophthalmic Assistant conducts measurements and tests that provide the Physician with the information needed to arrive at a diagnosis and to prescribe treatment.
Compensation
Compensation Range: $18.00-$34.68/hr (Dependent on Experience)
Responsibilities
Reviews patient charts to ensure completeness and accuracy of information.
Takes an ocular and systemic history and accurately records visual acuity.
Performs testing required by type of exam scheduled, patient complaint and history, including but not limited to OCT, automated visual fields, photography, pachymetry, biometry.
Performs lensometry, automated refractometry, slit lamp exam including applanation tonometry and anterior chamber angle assessment, basic muscle balance testing, assesses pupils, confrontation visual fields and gross external exam.
Performs advanced ophthalmic procedures.
Requirements
High School Graduate or General Education Degree (GED).
Bachelor’s degree in relevant discipline preferred.
The Research Assistant 1 HSS will be working in the Division of Family Planning in the Department of Obstetrics, Gynecology, and Reproductive Sciences supporting multiple clinical and translational research projects in reproductive health, including contraception and abortion.
Compensation
Hourly Range $28.43
Responsibilities
Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for designated research assignments
Records and compiles information related to research data
Codes data accordingly to research specifications
Uses a computer terminal to input and retrieve data and to generate reports
Processes and summarizes data using scientific or statistical techniques
Requirements
High school level education
Associate's degree
Bachelor's degree in a related field
Nice to have: Family planning research methodologies
As a Research Study Coordinator I, you will play a vital role in coordinating research projects within regulatory compliance guidelines. You will provide technical support to Principal Investigators, oversee recruitment, and manage day-to-day study operations.
Responsibilities
Reviews, interprets, and maintains knowledge of study protocols, procedures, timelines, and project requirements
Utilizes and maintains study-specific databases and tracking systems
Organizes and maintains study files, regulatory binders, source documentation, and research records
Coordinates research-related site visits, sponsor tours, and study meetings
Provides training, guidance, and operational support to research staff and study team members
Requirements
Bachelor's degree in a scientific discipline, Psychology, Sociology, Anthropology, Public Health, Healthcare Administration, or a related field
The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information.
Responsibilities
Obtain informed consent
Collect, maintain and organize study information
Assist in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office)
Collect and record study data
Input all information into database
Requirements
Bachelors or Masters degree in Science or closely related field
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