Clinical Research Coordinator - Part Time (Dr Gold's Lab) - Gastroenterology
Mount Sinai Health System
Invite-only right now: save jobs, track applications, build tailored resumesAlready have an account? Log in
- Location
- United States
- Job type
- Part time
- Posted
- Oct 15
- 5 days ago
Career path
See where this role leads
Jigup maps the next three moves from a job like this one, with the titles and the skills each step asks for.
About the company
Mount Sinai Health System
Hospital & health care · 10,001+ employees
What you'll do
- Conducts and assists with clinical research, including obtaining informed consent, screening and registering participants, and administering questionnaires.
- Collects and reviews data, maintains study records, and assists with grant and regulatory submissions.
What you need
- Bachelors degree in science or related field preferred or a combination of relevant research experience and education
- 0-2 years of research/human subjects experience
- Education: a bachelor's degree
Key skills
human subjects researchinformed consentresearch or interview techniques
Keywords for your resumePro
The words this employer's screening is likely to look for.
This job lists resume keywords
The terms this posting uses, pulled out so you can mirror them in your resume. Jigup Pro members see the list on the job board.
See full description on company page, apply now
Read the full posting here
The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and organizes study information. Assists in the preparation and submission of grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office).
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff.
Assists in the activities related to clinical research including, but not limited to: obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering questionnaires and answering telephone calls.
Assists in the collection, analysis and review of experimental data for publication and presentation.
Maintains source documents and subject files in accordance with Mount Sinai policies and procedures. Ensures accurate, confidential and complete compilation of data.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Performs other related duties