Clinical Research Associate I - Rheumatology

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Title:

Clinical Research Associate I - Rheumatology

Job ID:

93985

Location:

NJ 

Classification:

Administration, Education & Training, Healthcare & Community, I.T. & T., Manufacturing/Operations

Salary:

38-42

Salary Type:

per hour

Posted By:

The Veritas Healthcare Solutions LLC
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Job Type:

Full time

Posted:

10/07/2019

Start Date:

-

Telephone:

646-907-4086
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Job Description:

The Veritas Healthcare Solutions LLC is a rapidly growing E-Verified training and consulting company and we are currently looking for aspiring individuals to be trained and placed in Validation/DSA/PV/CRA/CDM/CDA/BA/QA. We offer Free online trainings and placement in respective fields. 

Visa Benefits provided for H1B, OPT, STEM OPT, CPT candidates.

Clinical Research Assoc I - Rheumatology

Essential duties and responsibilities:
  • Works with a Clinical Research Coordinator, Research Program Administrator, Research Nurse or Principal Investigator to coordinate/implement study.
  • Evaluates and abstracts clinical research data from source documents.
  • Ensures compliance with protocol and overall clinical research objectives.
  • Completes Case Report Forms (CRFs).
  • Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
  • Provides supervised contact with research participants or contact for long term follow-up research participants only.
  • Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
  • Schedules patients for research visits and research procedures.
  • Responsible for sample preparation and shipping and maintenance of study supplies and kits.
  • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
  • Maintains research practices using Good Clinical Practice (GCP) guidelines.
  • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • Participates in required training and education programs.
Department and/or unit specific essential job responsibilities:
  • Enters data from research subject charts into electronic data capture systems.
  • Assists with regulatory sponsor paperwork for clinical trials.
  • Chart abstraction for chart review studies.
  • Pre-screens potential subjects for various clinical trails.
  • Maintaining organization of various databases.
  • Tracks research participants for periodic required follow-up.
  • Maintains current addresses, contact info, phone numbers.
  • Attends internal research meetings, takes meeting minutes, maintains and distributes accurate minutes.
  • Maintaining organized files, and e-files.
  • Relaying/running documents between various offices.
  • Obtaining needed signatures on various research documents.
  • Organizing/scheduling/rescheduling research meetings.
  • Frequent communication with collaborating institutions; and other departments within the institution.
  • Maintain current contact information for research collaborators.

BENEFITS:

E-verification and initial OPT & STEM extension assistance.

H1b & GC sponsorship.

Relocation benefits.

Health benefits.

 

Interested candidates kindly send us your most recent resume.

Company Info
The Veritas Healthcare Solutions LLC 469 7th Ave
New York, NY, United States

Email: careers@theveritashealthcare.com
Phone: 646-907-4086
Web Site: http://www.theveritashealthcare.com/

Company Profile