drjobs Clinical Research Coordinator I- Pulmonary

Clinical Research Coordinator I- Pulmonary

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

New York City, NY - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Description

The Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Office).



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.
  • Screens patients for eligibility through medical record review and upcoming visit in the RI.
  • Assists in the activities related to clinical research studies including but not limited to: 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.
  • Assists with data analysis as needed.
  • Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
  • Secures delivers and ships clinical specimens as required by the protocol.
  • Prepares data for management meetings.
  • Performs other related duties.
  • Manages Study Data of Ongoing Clinical research projects Under Supervision of the Principal Investigator(s).
  • Ensure Proper Compliance with Institutional and Regulatory Requirements.
  • Attends weekly ILD meeting.
  • Assists the Principal Investigator(s) and regulatory staff in the preparation of new protocol submissions protocol amendments and renewals of ongoing clinical projects.
  • Working knowledge of Good Clinical Practice guidelines and Federal Research regulations.
  • Strong organizational and communications skills.
  • Comfort with communicating clinical information to medical personnel.
  • Ability to work on a team and individually.
  • Ability to identify analyze and solve problems while working under pressure.
  • Strong computer literacy.


Qualifications
  • Bachelors or Masters degree in Science or closely related field.
  • 1-2 years of research experience




Required Experience:

IC

Employment Type

Full-Time

Company Industry

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.