Clinical Research Coordinator jobs in Concord, NH
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
Clinical Research Coordinator II
- Dartmouth-Hitchcock Health
-
Lebanon, NH
FULL_TIME
-
Overview
**SIGN ON BONUS ELIGIBLE** Clinical Research Unit
This is available to external hires only for full time 40 hour positions only and certain conditions apply.
In order to qualify for a level II position you must have a Bachelors or equivalent years of experience, AND 2 years of post-college research experience, OR equivalent years of relevant experience. SOCRA or ACRP preferred.
Requires BLS certification within 30 days of hire. These positions are on site in Lebanon, NH.
Clinical Research Coordinator II performs a full range of clinical research duties at a skilled level and has a working knowledge of the clinical research process and the regulations that govern it. The expectation is to perform progressively more complex and comprehensive clinical research duties with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the supervision of and at the direction of the PI or their designee. They cannot perform any tasks that state or local law require a license to perform.
Responsibilities
- Research Operations – Occasionally requiring tasks outside of defined operating hours
- May arrange and/or schedule required tests and other appointments.
- Understands and supports all of aspects of the study operations (including subject management/regulatory) with oversight from the investigator or their designee.
- Primarily supports subject management, such as data entry in the Clinical Trial Management System(CTMS), scanning informed consents into EMR, and supporting data entry needs of the study.
- May carry out study visit tasks such as administering Quality of Life (QoL) questionnaires under supervision of investigator.
- May interview study participants about medical history, medications, adverse events, demographics, and quality of life issues depending on complexity with review by PI with collection of source data directly informed by medical records.
- May communicate with participants throughout the course of the study.
- May provide education and support to study participants and their families.
- Prepares and submits regulatory documents to study sponsors and applicable regulatory agencies.
- Maintains study and regulatory documentation.
- May manage study tasks primarily related to working with Institutional Review Boards (IRBs) and study sponsors as well as Dartmouth-Hitchcock Medical Center (DHMC) regulatory committees.
- Ethics & Participant Safety
- Applies and implements Good Clinical Practice (GCP)/Human Subjects Protection (HSP) practices.
- Maintains familiarity with the ethical conduct of research and safeguards needed when conducting research.
- May assist in the design of studies so they include specific safeguards to ensure ethical conduct and protect vulnerable populations.
- May develop or assist with the development of documents related to safety and security.
- May communicate with research participants regarding the difference between clinical activities and research activities, and the risks and benefits of study participation.
- Data and Informatics
- Utilizes the Electronic Data Capture (EDC) systems, technologies, and software necessary for study operations
- Scores tests, enter data, and completes Case Report Forms (CRFs, eCRFs) accurately and according to protocol.
- Develops or assists with the development of data collection documents and instruments and procedures for data quality assurance.
- Monitors for and identifies potential issues related to data capture, collection or management and suggests solutions. Investigates incomplete, inaccurate or missing data/documents to ensure accuracy and completeness of data.
- Adheres to processes and runs queries, summaries and reports to monitor the quality of data.
- May be responsible for recognizing trends related to data quality and escalating as appropriate.
- Uses required processes, policies and systems to ensure data security.
- Leadership and Professionalism
- Understands and employs the professional guidelines and code of ethics related to the conduct of clinical research and Dartmouth-Hitchcock (D-H) and project specific training requirements.
- May travel to investigator meetings or protocol specific training.
- May participate in new employee mentoring/training under the guidance of a supervisor or senior team member.
- Site and Study Management
- Organizes and manages clinical trials and research studies.
- Conducts protocol reviews to assess the feasibility of potential studies. Seeks out new research opportunities.
- Participates in study site selection activities.
- Collaborates with study investigators to develop recruitment and screening procedures.
- Designs and develops recruitment documentation.
- Composes informed consent forms and protocol abstracts.
- Maintains other study documents and study management tools.
- May participate in manuscript/abstract development.
- Communication and Team Science
- Serves as a liaison between principal investigators, regulatory agencies, D-H stakeholders and study participants to resolve problems.
- Identifies and recognizes the respective roles of team members.
- Understands and upholds the importance of an interdisciplinary team and the value each member can bring to clinical studies.
- Bachelors 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
- BLS certification required within 30 days of hire
- 11 Days Ago
Performs other duties as required or assigned.
Qualifications
Required Licensure/Certifications
Clinical Research Coordinator III
- Dartmouth-Hitchcock Health
-
Lebanon, NH
FULL_TIME
- Overview SIGN ON BONUS ELIGIBLE The Clinical Research Coordinator III performs a full range of clinical research duties at an advanced level and plans, organizes, leads, and performs comprehensive cli...
- 1 Month Ago
Clinical Research Coordinator I
- Dartmouth-Hitchcock Health
-
Lebanon, NH
FULL_TIME
- 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 Coor...
- 1 Month Ago
Research Coordinator
- Dartmouth College
-
Hanover, NH
FULL_TIME
- Position Information Posting date 03/27/2024 Closing date Open Until Filled Yes Position Number 1128821 Position Title Research Coordinator Department this Position Reports to Center for Technology an...
- 26 Days Ago
Clinical Research Assistant
- NH Oncology-Hematology, P.A.
-
Concord, NH
FULL_TIME,PART_TIME
- Full-time (40 hrs/wk), Clinical Research Associate position available at a regional medical oncology practice. We are looking for a highly motivated individual to complete data collection and provide ...
- 15 Days Ago
Clinical Research Nurse II
- Dartmouth-Hitchcock Health
-
Lebanon, NH
FULL_TIME
- Overview Clinical Research Nurse II performs a full range of clinical and non-clinical research duties, and has a working knowledge of the clinical research process and the regulations that govern it....
- 1 Month Ago
Filters
- Current Active Filter
- Concord, NH
Clear All
- Filter Jobs By posted time
- Within 1 Day
- Within 2-7
- Within 1 Month
- Within 3 Months
0 Clinical Research Coordinator jobs found in Concord, NH area
Clinical Nurse Leader
- DMC Primary Care
-
Derry Village, NH
- Job Description Job Description Join our Team! DMC Primary Care, a physician-owned, independent practice, with offices t...
- 4/25/2024 12:00:00 AM
Clinical Nurse Coordinator Emergency Room
- Hiring Now!
-
Derry, NH
- Description Introduction Parkland Medical Center is committed to investing in the latest technology enabling nurses to w...
- 4/25/2024 12:00:00 AM
Clin Nurse Coordinator Free Standing ED Plaistow
- Hiring Now!
-
Derry, NH
- Description Introduction Parkland Medical Center is committed to investing in the latest technology enabling nurses to w...
- 4/25/2024 12:00:00 AM
Travel MRI Technologist - $2,880 per week
- Hiring Now!
-
Concord, NH
- LeaderStat is seeking a travel MRI Technologist for a travel job in Concord, New Hampshire. Job Description & Requiremen...
- 4/25/2024 12:00:00 AM
Patient Safety Coordinator
- HCA
-
Portsmouth, NH
- Introduction Do you want to be appreciated daily? Our nurses are celebrated for being on the front line, empathetic for ...
- 4/24/2024 12:00:00 AM
NH Inpatient RN Care Manager
- HexaQuEST Health, Inc.
-
Concord, NH
- Summary The Inpatient Nurse Care Manager, in collaboration with the multidisciplinary team is responsible for assessing,...
- 4/24/2024 12:00:00 AM
Travel CT Technologist - $3,556 per week
- Hiring Now!
-
Concord, NH
- LeaderStat is seeking a travel CT Technologist for a travel job in Concord, New Hampshire. Job Description & Requirement...
- 4/24/2024 12:00:00 AM
Travel Pharmacist - $3,009 per week
- Hiring Now!
-
Concord, NH
- MedPro Healthcare Allied Staffing is seeking a travel Pharmacist for a travel job in Concord, New Hampshire. Job Descrip...
- 4/24/2024 12:00:00 AM
About Concord, New Hampshire
Concord is located at 43°12′24″N 71°32′17″W / 43.20667°N 71.53806°W / 43.20667; -71.53806 (43.2070, −71.5371).
According to the United States Census Bureau, the city has a total area of 67.5 square miles (174.8 km2). 64.2 square miles (166.4 km2) of it is land and 3.2 square miles (8.4 km2) of it is water, comprising 4.79% of the city. Concord is drained by the Merrimack River. Penacook Lake is in the west. The highest point in Concord is 860 feet (260 m) above sea level on Oak Hill, just west of the hill's 970-foot (300 m) summit in neighboring Loudon.
Concord lies fully within the Merrima...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$62,005 to $83,606
Concord, New Hampshire area prices
were up 1.4% from a year ago
were up 1.4% from a year ago
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Monterey, CA
Coordinators often become the front line for patients because they feel more comfortable with us.
November 07, 2019
Clinical Research Coordinator in Bakersfield, CA
If you have a medical experience you may need a certificate program to work as a CRC bt if there is none then you will need an education program that covers all the required medical and research coursework in clinical research.
October 27, 2019
Clinical Research Coordinator in New Bedford, MA
If you’re looking for a job you can complete at home that lets you use your organizational and leadership skills, a career in clinical research coordination could be for you.
October 09, 2019