Clinical Research Coordinator jobs in Delaware
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-Onsite
- Sigma Inc
-
Newark, DE
CONTRACTOR,FULL_TIME
-
FM17016 Clinical Research Coordinator,Newark, DE, 6 Months
Sigma Inc is currently looking for a Clinical Research Coordinator to work onsite in Newark, DE
Shift timings:
6 month contract with potential to convert based on performance. Onsite position. M-F but some Saturday may be needed. Typically 8am- 5pm but may need to flex earlier to meet patients.
Responsibilities:
General Administrative:
Continues to display a mastery of Senior Clinical Research Associate duties and responsibilities
Adheres to Standard Operating Procedures (SOP), GCP, all regulatory practices as established by law, and company policies and procedures
Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with Food and Drug Administration (FDA), GCP, and ICH Guidelines
In collaboration with the PI, incorporates knowledge of protocol to identify potential study participants according to inclusion/exclusion criteria
Develops processes for monitoring the status of study subjects as they progress through the study protocol assessment timeline
Maintains up-to-date knowledge for operation and use of study specific equipment and technology
Participates in the ongoing informed consent process, ensuring that human subjects, their families, and other health care providers clearly understand what is expected of them during participation in a clinical trial
Serves as an advocate for human subjects by establishing rapport with participants through open, transparent communication
Educates the subject on study protocol and procedures
Maintains the study site files according to GCP
Maintains subject participant records according to GCP
Demonstrates initiative and actively seeks new opportunities for continuous learning by attendance at educational and professional development training opportunities .
Conduct of Research:
Reviews source document templates for protocol accuracy identifying any errors or improvements needed to be made for data integrity prior to subject screening
Performs tasks required by a protocol, which may include obtaining medical history, phlebotomy, Electrocardiogram (EKG), and other required tests, assessments, or procedures
Develops in depth knowledge of study-specific requirements for reporting subject safety issues to the sponsor, institutional review board (IRB), FDA, and other regulatory agencies.
Monitors, detects, and reports adverse events per the requirements of the sponsor, regulatory bodies, and site policies. Coordinates and gathers information from a variety of sources to ensure subject safety
Prepares and submits regulatory documents in an accurate and timely manner under the supervision of the PI and appropriate management
Utilizes or acquires knowledge of disease processes to recognize -subject's change(s) in condition
Regularly evaluates the study subjects' condition and communicates concerns, with documented follow up to the PI, to ensure subject safety
Accurately documents study subject activities as it pertains to the clinical study according to the principals of ALCOA (Attributable, Legible, Contemporaneous, Original, Accurate)
Maintains environmental integrity for investigational study product, administration, accountability, and storage according to study protocol and sponsor requirements
Ensures appropriate storage, access, and maintenance of records pertaining to investigational product
Conducts routine assessments to evaluate the subject's response to and adherence to investigational product orders, and communicates observations/results to the PI, sponsor, and IRB as appropriate
Consults with PI regarding the appropriate administration of investigational product
Administers the investigational product according to the parameters of the study protocol, including local law, and under the direction of the physician
Ensures safe handling of biological specimens
Meets with the study monitor to review, verify, and correct all data entered onto the case report form and to ensure appropriate maintenance of study records
Conducts ongoing assessments of the overall study execution within the facility/practice, communicating concerns to the Director, PI, study sponsor or IRB as needed
Financial Management:
Tracks and coordinates potential site study subject stipend disbursement
Ensures appropriate billing charge documents are submitted for reimbursement
Requirements
Bachelor's Degree or an equivalent combination of education and experience.
2 years' healthcare experience with Renal experience preferred. Research experience preferred
Willing to pursue CCRC or SoCRA certification when eligible.
Current appropriate state licensure if applicable.
Proficient with PCs and Microsoft Office applications.
Good communication and organizational skills.
Ability to work independently.
- 11 Days Ago
Clinical Research Coordinator
- Aledade
-
Wilmington, DE
FULL_TIME
- Aledade, a public benefit corporation, exists to empower the most transformational part of our health care landscape - independent primary care. We were founded in 2014, and since then, we've become t...
- 12 Days Ago
Clinical Research Coordinator
- NemoursCareerSite
-
Wilmington, DE
FULL_TIME
- The Center for Healthcare Delivery Science (CHDS) at Nemours Children’s Health is seeking a full-time Bilingual Research Coordinator (RC). Bilingual (English/Spanish) communication skills are strongly...
- 1 Month Ago
Clinical Research Coordinator - Bilingual
- NemoursCareerSite
-
Wilmington, DE
FULL_TIME
- The Center for Healthcare Delivery Science (CHDS) at Nemours Children’s Health is seeking a full-time Bilingual Clinical Research Coordinator (CRC). Bilingual (English/Spanish) communication skills ar...
- 2 Months Ago
Clinical Research Coordinator, PET MRI center
- NemoursCareerSite
-
Wilmington, DE
PART_TIME
- Nemours is seeking a part-time Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE. For the Nemours Radiology Enterprise, coordinates, implements and completes c...
- 24 Days Ago
Clinical Research Coordinator-PET MRI center
- NemoursCareerSite
-
Wilmington, DE
FULL_TIME
- The Radiology Department is seeking a full-time Clinical Research Coordinator to be based in Wilmington, DE. The Research Coordinator will facilitate the growth and conduct of research in Radiology by...
- 28 Days Ago
Clinical Research Coordinator jobs at Popular Companies
Clinical Research Coordinator
- CARLE
-
Peoria, IL
- Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
- 4/25/2024 12:00:00 AM
Clinical Research Coordinator/Clinical Research Coordinator, Licensed
- Virginia Commonwealth University
-
Richmond, VA
- Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of R...
- 4/25/2024 12:00:00 AM
Clinical Research Coordinator
- Investigators Research Group, LLC
-
Brownsburg, IN
- Company Description Investigators Research Group, LLC is a growing network of Investigators and healthcare professionals...
- 4/25/2024 12:00:00 AM
Clinical Research Coordinator
- Barrington James
-
Columbia, MO
- Are you looking for an opportunity to grow in the clinical research world? Barrington James is looking for Clinical Rese...
- 4/25/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Urbana, IL
- The hEDS GENE Study is looking for a data analyst to assist in its ongoing efforts to identify genes associated with the...
- 4/24/2024 12:00:00 AM
Senior Clinical Research Coordinator
- Abbott Laboratories
-
South Portland, ME
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
- 4/24/2024 12:00:00 AM
Clinical Research Coordinator
- Nuvance Health
-
Norwalk, CT
- Clinical Research Coordinator, Norwalk, CTFull-time, 40 hours - 8:30 am - 5:00 pmNuvance Health has a network of conveni...
- 4/24/2024 12:00:00 AM
Clinical Research Coordinator
- Beth Israel Lahey Health
-
Boston, MA
- When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. Job Typ...
- 4/21/2024 12:00:00 AM
About Delaware
Delaware is 96 miles (154 km) long and ranges from 9 miles (14 km) to 35 miles (56 km) across, totaling 1,954 square miles (5,060 km2), making it the second-smallest state in the United States after Rhode Island. Delaware is bounded to the north by Pennsylvania; to the east by the Delaware River, Delaware Bay, New Jersey and the Atlantic Ocean; and to the west and south by Maryland. Small portions of Delaware are also situated on the eastern side of the Delaware River sharing land boundaries with New Jersey. The state of Delaware, together with the Eastern Shore counties of Maryland and two co...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$60,983 to $82,229
Most Popular Cities in Delaware 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