Clinical Research Coordinator jobs in New Hampshire
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
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
-
Department: Operations
Employment Type: Full Time
Location: ActivMed Practices & Research | Portsmouth, NH
Reporting To: Christopher Lenox
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
Key Responsibilities
In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
Under The Direction Of The Site Manager/Director And The Principal/Sub Investigators, Conducts The Following According To Study Protocol, Company Processes & Procedures, And In Compliance With FDA, GCP, ICH Regulations And Guidelines- Screening of patients for study enrollment;
- Patient consents;
- Patient follow-up visits;
- Documenting in source clinic charts;
- Entering data in EDC and answers queries;
- Obtaining vital signs and ECGs;
- May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
- Requesting and tracking medical record requests;
- Updating and maintaining logs, chart filings;
- Maintaining & ordering study specific supplies;
- Scheduling subjects for study visits and conducts appointment reminders;
- Building/updating source as needed;
- Conducting monitoring visits and resolves issues as needed in a timely manner;
- Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
- Filing SAE/Deviation reports to Sponsor and IRB as needed;
- Documenting and reporting adverse events;
- Reporting non-compliance to appropriate staff in timely manner;
- Maintaining positive and effective communication with clients and team
- Always practicing ALCOAC principles with all documentation;
- Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
- Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
- Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
- Assist with training of new research assistants and coordinators;
- Assist with scheduling and planning for visit capacity for assigned studies;
- May set up, train and maintain all technology needed for studies;
- May assist with study recruitment, patient enrollment, and tracking as needed;
- May handle more complex study assignments and volumes;
- May participate in community outreach / education events;
- Maintaining confidentiality of patients, customers and company information, and;
- Performing all other duties as requested or assigned.
Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential AND 2 years of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills- Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm);
- Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
- Strong organizational skills and attention to detail.
- Well-developed written and verbal communication skills.
- Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
- Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
- Must be professional, respectful of others, self-motivated, and have a strong work ethic.
- Must possess a high degree of integrity and dependability.
- Ability to work under minimal supervision, identify problems and implement solutions.
- Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
- Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
- Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
- 5 Days Ago
Clinical Research Assistant / EMT
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanza is a growing multi-site, multi-phase clinical ...
- 11 Days Ago
Clinical Research Assistant / Medical Assistant
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanza is a growing multi-site, multi-phase clinical ...
- 4 Days Ago
Medical Assistant / Clinical Research Assistant
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Medical Assistant / Clinical Research AssistantDepartment: Operations Employment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanz...
- 20 Days Ago
Clinical Research Patient Recruiter (Patient Registrar) - onsite
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Clinical Research Patient Recruiter (Patient Registrar) - onsiteDepartment: Patient Recruitment Employment Type: Full TimeLocation: ActivMed Practices & Research | Pease, NHDescriptionAlcanza is a gro...
- 26 Days Ago
Clinical Research Coordinator I
- Dartmouth Health
-
Lebanon, NH
FULL_TIME
- OverviewClinical 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 Coord...
- 9 Days Ago
Clinical Research Coordinator jobs at Popular Companies
Clinical Research Coordinator
- Advarra
-
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Clinical Research Coordinator
- Advarra
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Clinical Research Coordinator
- Sanford Health
-
Fargo, ND
- Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
- 6/10/2024 12:00:00 AM
Clinical Research Coordinator
- Danbury Health Systems
-
Norwalk, CT
- Clinical Research Coordinator, Norwalk, CT Full-time, 40 hours; 8:30 am - 5:00 pm Nuvance Health has a network of conven...
- 6/10/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Peoria, IL
- Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
- 6/9/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Urbana, IL
- The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the dail...
- 6/8/2024 12:00:00 AM
Clinical Research Coordinator
- Sanford Health
-
Sioux Falls, SD
- Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
- 6/8/2024 12:00:00 AM
Clinical Research Coordinator
- Hackensack Meridian Health
-
Nutley, NJ
- Overview: Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients liv...
- 6/7/2024 12:00:00 AM
About New Hampshire
New Hampshire is part of the six-state New England region. It is bounded by Quebec, Canada, to the north and northwest; Maine and the Atlantic Ocean to the east; Massachusetts to the south; and Vermont to the west. New Hampshire's major regions are the Great North Woods, the White Mountains, the Lakes Region, the Seacoast, the Merrimack Valley, the Monadnock Region, and the Dartmouth-Lake Sunapee area. New Hampshire has the shortest ocean coastline of any U.S. coastal state, with a length of 18 miles (29 km), sometimes measured as only 13 miles (21 km). New Hampshire was home to the rock forma...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$61,373 to $82,752
Most Popular Cities in New Hampshire for Clinical Research Coordinator Jobs
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019