Clinical Research Coordinator jobs in Wilmington, DE
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
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, 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
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0 Clinical Research Coordinator jobs found in Wilmington, DE area
Clinical Research Coordinator
- Nemours Foundation
-
Wilmington, DE
- The Center for Healthcare Delivery Science (CHDS) at Nemours Children's Health is seeking a full-time Bilingual Research...
- 4/24/2024 12:00:00 AM
Clinical Research Coordinator A
- The University of Pennsylvania
-
Philadelphia, PA
- University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned le...
- 4/24/2024 12:00:00 AM
Clinical Research Coordinator
- Nemours Children's Health
-
Wilmington, DE
- Job Description Nemours Children's Hospital Delaware is seeking a Clinical Research Coordinator to support clinical rese...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator - Oncology
- Tower Health
-
Philadelphia, PA
- Responsibilities: The Oncology Research Coordinator at the St. Christopher's Hospital for Children will be a crucial add...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator
- The University of Pennsylvania
-
Philadelphia, PA
- University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned le...
- 4/22/2024 12:00:00 AM
Clinical Research Coordinator
- Proclinical Staffing
-
Philadelphia, PA
- Clinical Research Coordinator - Philadelphia, PA - Permanent Proclinical is seeking a dedicated and organized Clinical R...
- 4/22/2024 12:00:00 AM
Clinical Research Coordinator 224989
- Medix™
-
Pennsauken, NJ
- We are looking for a Clinical Research Coordinator to join our growing team! This is a full time onsite role that requir...
- 4/22/2024 12:00:00 AM
Clinical Research Coordinator
- Proclinical Staffing
-
Philadelphia, PA
- Clinical Research Coordinator - Philadelphia, PA - Permanent Proclinical is seeking a dedicated and organized Clinical R...
- 4/20/2024 12:00:00 AM
About Wilmington, Delaware
According to the United States Census Bureau, the city has a total area of 17.0 square miles (44 km2). Of that, 10.9 square miles (28 km2) is land and 6.2 square miles (16 km2) is water. The total area is 36.25% water.
The city sits at the confluence of the Christina River and the Delaware River, about 33 miles (53 km) southwest of Philadelphia. Wilmington Train Station, one of the southernmost stops on Philadelphia's SEPTA rail transportation system, is also served by Northeast Corridor Amtrak passenger trains. Wilmington is served by I-95 and I-495 within city limits. In addition, the twin-s...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$62,665 to $84,497
Wilmington, Delaware area prices
were up 1.0% from a year ago
were up 1.0% 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