7 Results for

Clinical Research Associate Jobs in New Hampshire

Jobs

NH18 days ago

p>Research Operations - Occasionally requiring tasks outside of defined operating hours:

Mentors, onboards, trains and oversees new clinical research coordinator staff on Good Clinical Practice (GCP), Human Subjects Protection (HSP) practices, the ethical conduct of research and a full range of clinical research duties including regulatory compliance.

The Clinical Research Coordinator III performs a full range of clinical research duties at an advanced level and plans, organizes, leads, and performs comprehensive clinical trial duties for multiple or complex clinical trials, focusing on the overall productivity and success of the program.

Lebanon, New Hampshire19 days ago

Responsibilities: Research Operations - Occasionally requiring tasks outside of defined operating hours: Mentors, onboards, trains and oversees new clinical research coordinator staff on Good Clinical Practice (GCP), Human Subjects Protection (HSP) practices, the ethical conduct of research and a full range of clinical research duties including regulatory compliance. Overview: The Clinical Research Coordinator III performs a full range of clinical research duties at an advanced level and plans, organizes, leads, and performs comprehensive clinical trial duties for multiple or complex clinical trials, focusing on the overall productivity and success of the program.

NH18 days ago

Tracks all required essential regulatory documents according to International Council on Harmonization (ICH) Good Clinical Practice (GCP) guidelines including but not limited to: investigators' Curriculum Vitae (CVs), medical licenses, Collaborative Institutional Training Initiative (CITI), clinical laboratory certifications, etc. Primarily supports subject management, such as subject visit preparation, performs data entry in the Clinical Trial Management System (CTMS), scans informed consents into Electronic Medical Record (EMR) and supports data entry needs of the study.

Lebanon, New Hampshire19 days ago

li>Tracks all required essential regulatory documents according to International Council on Harmonization (ICH) Good Clinical Practice (GCP) guidelines including but not limited to: investigators’ Curriculum Vitae (CVs), medical licenses, Collaborative Institutional Training Initiative (CITI), clinical laboratory certifications, etc.

Primarily supports subject management, such as subject visit preparation, performs data entry in the Clinical Trial Management System (CTMS), scans informed consents into Electronic Medical Record (EMR) and supports data entry needs of the study.

Manchester, New Hampshire30+ days ago

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Competencies and Personal Traits:

What We Do:
- Execution Excellence: Ability to set goals, create structure and maintain a focused and collaborative approach to the delivery of timely and high-quality work.
- Why We Do It:
  - Seek Meaning and Purpose and a Desire to be Part of Something Bigger than Yourself: Crave being part of a team that works together under shared values to achieve significant positive impact in the wider world.

NH18 days ago

Lebanon, New Hampshire19 days ago

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Clinical Research Associate Jobs in New Hampshire

Research Coordinator III Clinical Research Units Dartmouth-Hitchcock Medical Center

Research Coordinator III - Clinical Research Units Dartmouth-Hitchcock Health

Research Coordinator I Clinical Research Units Dartmouth-Hitchcock Medical Center

Research Coordinator I - Clinical Research Units Dartmouth-Hitchcock Health

Clinical Research Coordinator I Ora

Research Coordinator I Ortho Dartmouth-Hitchcock Medical Center

Research Coordinator I - Ortho Dartmouth-Hitchcock Health

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