Top 29 Clinical research Jobs in Hanover, Nh

Research Coordinator I - Dermatology
Dartmouth-Hitchcock —Lebanon, NH
- $19.20 - $29.76 an hour
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- Entry level
- Disability insurance
- Health insurance
6d
Research Clinical Coordinator (CONFIRM) - White River Junction, VT
US Department of Veterans Affairs —White River Junction, VT
- $57,150 - $90,882 a year
- Full-time
- Microsoft Excel
- Microsoft Access
- Microsoft Outlook
- Health savings account
- Health insurance
Quick Apply
9d
Research Assistant I
Dartmouth College —Hanover, NH
- $20 - $23 an hour
- Full-time
- Background check
- Writing skills
- Laboratory experience
Research Coordinator I - Surgery
Dartmouth-Hitchcock —Lebanon, NH
- $19.20 - $29.76 an hour
- Full-time
- Surgery
- BLS Certification
- Bachelor's degree
- Disability insurance
- Health insurance
Research Coordinator II - Gastroenterology
Dartmouth-Hitchcock —Lebanon, NH
- $46,321.60 - $71,780.80 a year
- Full-time
- Mid-level
- Bachelor's degree
- Quality control
- Disability insurance
- Health insurance
13d
Research Project Coordinator
Dartmouth College —Hanover, NH
- $57,100 - $71,570 a year
- Full-time
- Background check
- 5 years
- Writing skills
- COVID-19 protective measures
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Lebanon, NH
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification
Undergraduate HTE Research Co-op (January - June 2027)
Adimab —Lebanon, NH
- Weekends as needed
- Research
- Entry level
Quick Apply
Project Manager
Dartmouth College —Hanover, NH
- $75,700 - $94,700 a year
- Full-time
- Background check
- Computer science
- Computer Science
Research PostDoctoral Fellow
Dartmouth-Hitchcock —Lebanon, NH
- Full-time
- Management
- English
- Doctor of Philosophy
- Disability insurance
- Health insurance
10d
Postdoctoral Fellow Molecular Diagnostics
Dartmouth-Hitchcock —Lebanon, NH
- Full-time
- Senior level
- Disability insurance
- Health insurance
Pediatric Registered Nurse (RN), Research Nurse I - Cancer Center
Dartmouth-Hitchcock —Lebanon, NH
- $78,520 - $110,760 a year
- Full-time
- Nursing
- RN License
- Hospital
- Disability insurance
- Health insurance
Staff Fellow, Wilderness and Austere Medicine
Dartmouth-Hitchcock —Lebanon, NH
- Full-time
- Medicine
- Hospital
- BC/BE
Anesthesiologist - Dartmouth-Hitchcock Medical Center
Dartmouth-Hitchcock —Lebanon, NH
- Full-time
- Pediatrics
- Pediatrics
- Senior level
- Disability insurance
- Relocation assistance
Mobile Clinical & Life Insurance Phlebotomist
APPS Paramedical Services —South Royalton, VT
- $20 - $23 an hour
- Part-time
- Bilingual
- RN License
- Driver's License
- Life insurance
Quick Apply
Weight Center Obesity Medicine Fellow 2027
Dartmouth-Hitchcock —Lebanon, NH
- Full-time
- Medicine
- Mid-level
- Analysis skills
- Disability insurance
- Health insurance
Medical Oncologist
Dartmouth-Hitchcock —Lebanon, NH
- $2,080 - $475,000 a year
- Full-time
- Medicine
- Hospital
- BC/BE
- Disability insurance
- Health insurance
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —United States
- $103,326 - $133,200 a year
- Full-time
- Research
- Mid-level
- Bachelor's degree
MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years

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Part-Time Endocrinology Research Physician Opportunity in Columbus, Ohio
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Comprehensive research infrastructure and operational support provided at no cost to your practice. Continue your regular patient schedule while identifying…
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State of Ohio - Medicaid —Columbus, OH
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Research Coordinator I - Dermatology

Dartmouth-Hitchcock -
Lebanon, NH

Apply Now

Job Details

Full-time
$19.20 - $29.76 an hour
6 days ago

Benefits

Disability insurance
Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance
Retirement plan

Qualifications

ICH guidelines

Full Job Description

Overview

Clinical Research Coordinator I works closely with other research staff and is involved at a fundamental level to support basic administrative clinical trial tasks. The Clinical Research Coordinator I has no supervisory responsibilities and works under direct supervision of the Principal Investigator or designee. They cannot perform any tasks that by state or local law require a license to perform.

Responsibilities

Research Operations

May arrange/schedule required appointments.

Learns and supports all of aspects of the study operations (subject management/regulatory) with substantial oversight from the investigator or their designee.

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.

Regulatory Affairs

Assists with compiling and maintaining essential records and documents required by Dartmouth-Hitchcock Medical Center (DHMC) and various sponsor organizations in compliance with applicable standards operating procedures for the execution of clinical trial operations, including timely Institutional Review Board (IRB) submissions meeting sponsor and departmental requirements.

Provides support to supervisor and IRB with regard to regulatory and sponsor-related issues.

Assists with maintaining accurate and timely sponsor communications regarding status of research studies.

Under the direction of the supervisor, assists DMHC investigators with regulatory processes.

Maintains basic current understanding of IRB and Dartmouth-Hitchcock Health (D-HH) Institutional processes.

Maintains and tracks on-site and off-site storage of required study records and assists with data entry and accurate use of a tracking system for maintaining required essential documents.

Assists with local and commercial IRB, including initial submissions, modifications, renewal applications, and study closeout procedures.

Assists with scheduling and coordination of site visits, participates in site visits as assigned and tracks and ensures action items noted during site visits are completed and closed.

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.

Ethics & Participant Safety

Adheres to the principles for the ethical conduct of research, and safeguards for protection of human subjects especially when conducting research with vulnerable populations.

Understands and prioritizes the safety of research participants.

Data and Informatics

Utilizes Electronic Data Capture (EDC) systems, technologies and software necessary for study operations.

Completes data entry related to test results and/or measures according to protocol, and appropriate to role. Completes paper and electronic Case Report Forms (CRFs and eCRFs) accurately and according to protocol.

Assists with investigating incomplete, inaccurate or missing data and or documents to ensure accuracy and completeness of data; follows Standard Operating Procedures (SOPs) for data quality assurance.

Appropriately utilizes standard processes, policies and systems to ensure data integrity, attribution, and security.

Leadership and Professionalism

Understands and demonstrates the professional guidelines and code of ethics related to the conduct of clinical research.

Completes all D-H and project-specific training requirements.

Site and Study Management

Assists with administrative tasks associated with clinical research studies (e.g. document and supply management).

Maintains lab kits and creates and maintains regulatory and subject binders.

May participate in manuscript/abstract development.

Communication and Team Science

Communicates appropriately (written and orally) between stakeholders.

Assists with communications between principal investigators, regulatory agencies, D-H stakeholders and study participants to resolve problems.

Performs other duties as required or assigned.

Qualifications

Bachelor's degree or the equivalent combination of education and experience required.

Required Licensure/Certifications

- BLS certification within 30 days of hire date. - Human Subject Protection, Responsible Conduct of Research and Good Clinical Practice certificates required within 30 days of hire.

Area of Interest: Research/Science
Pay Range: $19.20/Hr. - $29.76/Hr.
FTE/Hours per pay period: 1.00 - 1.00 - 40 hrs/week
Shift: Day
Job ID: 40903

Dartmouth Health offers a total compensation package that includes a comprehensive selection of benefits. Our Core Benefits include medical, dental, vision and life insurance, short and long term disability, paid time off, and retirement plans. Click here for information on these benefits and more: Benefits | DHMC and Clinics Careers

Dartmouth Health is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Apply Now

Refine Your Search

clinical research jobs in hanover, nh

Research Coordinator I - Dermatology

Research Clinical Coordinator (CONFIRM) - White River Junction, VT

Research Assistant I

Research Coordinator I - Surgery

Research Coordinator II - Gastroenterology

Research Project Coordinator

Per Diem Clinical Research Nurse - Home Visits

Undergraduate HTE Research Co-op (January - June 2027)

Project Manager

Research PostDoctoral Fellow

Postdoctoral Fellow Molecular Diagnostics

Pediatric Registered Nurse (RN), Research Nurse I - Cancer Center

Staff Fellow, Wilderness and Austere Medicine

Anesthesiologist - Dartmouth-Hitchcock Medical Center

Mobile Clinical & Life Insurance Phlebotomist

Weight Center Obesity Medicine Fellow 2027

Medical Oncologist

Special Agent: Healthcare Services/Medical Background

MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA

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