Clinical Research Coordinator II: Independent Study Operations & Data

Dartmouth-Hitchcock Health

Lebanon (NH)

On-site

USD 60,000 - 90,000

Full time

8 days ago
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Job summary

Dartmouth-Hitchcock Health in Lebanon, NH seeks a Clinical Research Coordinator II to perform a full range of clinical research duties under PI supervision. You'll manage data entry in CTMS, handle regulatory documents, and support study visits.

You will ensure compliance with GCP/HSP, assist with ethics submissions, and interact with participants, investigators, and sponsors. A bachelor's degree and related experience are required; travel may be needed.

Qualifications

  • Bachelor's degree and 2 years of relevant research experience OR equivalent years of experience.
  • Ability to travel as required.
  • SOCRA/ACRP Certification or eligible for certification preferred.

Responsibilities

  • Schedule required tests and appointments.
  • Support subject management and regulatory activities with oversight from PI.
  • Data entry in CTMS and CRFs; maintain study data accuracy.
  • Administer QoL questionnaires under supervision.
  • Interview study participants about medical history, medications, adverse events, demographics, and QoI issues as applicable.
  • Communicate with participants throughout the study.
  • Provide education and support to participants and families.
  • Prepare and submit regulatory documents to sponsors and regulators.
  • Maintain study and regulatory documentation.
  • Assist with IRB and regulatory committee tasks as needed.

Skills

Travel ability
Interpersonal skills
Attention to detail

Education

Bachelor's degree or equivalent experience

Tools

CTMS

Job description

Dartmouth-Hitchcock Health in Lebanon, NH seeks a Clinical Research Coordinator II to perform a full range of clinical research duties under PI supervision. You'll manage data entry in CTMS, handle regulatory documents, and support study visits.

You will ensure compliance with GCP/HSP, assist with ethics submissions, and interact with participants, investigators, and sponsors. A bachelor's degree and related experience are required; travel may be needed.

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