Clinical Research Coordinator jobs in Newark, NJ
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 III
- DM Clinical Research
-
Jersey, NJ
FULL_TIME
-
Clinical Research Coordinator III
A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES- Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
- Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- Sponsor-provided and IRB-approved Protocol Training
- All relevant Protocol Amendments Training
- Any study-specific Manuals Training, as applicable
- Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
- Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
- Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
- Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
- Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
- Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
- Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
- Ability to train and mentor site staff, as needed
- Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
- Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
- Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
- Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
- Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
- Being prepared for and available at all required company meetings.
- Submitting required administrative paperwork per company timelines.
- Occasionally attending out-of-town Investigator Meetings
- Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
- Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
- Facilitate effective communication between patients, healthcare providers, and research staff
- Any other matters as assigned by management
KNOWLEDGE & EXPERIENCE
Education:- High School Diploma or equivalent required
- Bachelor's degree preferred
- Foreign Medical Graduates preferred
- Minimum of 5 years experience in Clinical Research
- Supervisory experience preferred
- Wide therapeutic range of clinical trials experience preferred
- Regulatory research experience is a plus
- ACRP or equivalent certification is preferred
- Goals-driven while continuously maintaining quality.
- Must be detailed-oriented, proactive, and able to take initiative.
- Must have strong written and communication skills.
- Must have excellent customer service skills.
- Proficient communication and comprehension skills both verbal and written in the English language are required.
- Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
- Just Posted
Travel Clinical Research Coordinator
- Care Access
-
Newark, NJ
FULL_TIME
- What We Do Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physici...
- 27 Days Ago
Jr. Clinical Research Coordinator
- SGS
-
Union, NJ
FULL_TIME
- Company DescriptionWe are SGS – the world’s leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 97,000 emplo...
- 1 Month Ago
CRC III
- DM Clinical Research
-
Jersey, NJ
FULL_TIME
- Clinical Research Coordinator III The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regu...
- 1 Month Ago
Clinical Research Coordinator - Florham Park NJ
- 5PY US Quintiles, Inc.
-
Florham Park, NJ
PART_TIME
- Are you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression? If so...
- 24 Days Ago
Nurse Coordinator - Trauma Program
- Clinical Management Consultants
-
Bayonne, NJ
FULL_TIME
- Are you ready to take your nursing career to the next level while making a meaningful impact in one of New York's premier healthcare systems? A highly reputable 400 bed acute care hospital system in t...
- 16 Days Ago
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0 Clinical Research Coordinator jobs found in Newark, NJ area
Clinical Research Coordinator
- NYU Langone Health
-
New York, NY
- NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
- 4/24/2024 12:00:00 AM
Clinical Research Coordin
- PRISM Vision Group
-
Teaneck, NJ
- Summary: The Clinical Research Coordinator reports to the Manager of Clinical Research and will aid in the coordination ...
- 4/24/2024 12:00:00 AM
Clinical Research Coordinator
- Schwarzman Animal Medical Center
-
New York, NY
- Department: Clinical Services Clinical Research Coordinator Clinical Research Coordinator Summary The Schwarzman Animal ...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator - 224988
- Medix™
-
Elizabeth, NJ
- Medix is hiring a contract Clinical Research Coordinator in Elizabeth, NJ to support decentralized research trials! This...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator
- Emerson Clinical Research Institute
-
Passaic, NJ
- Job Description Job Description Our clinical research company is looking to hire a qualified candidate for the full-time...
- 4/22/2024 12:00:00 AM
Clinical Research Coordinator
- Insight Global
-
Newark, NJ
- Insight Global is looking for a Clinical Research Coordinator for our higher education healthcare client in Newark, NJ. ...
- 4/22/2024 12:00:00 AM
Clinical Research Coordinator
- Northwell Health
-
New Hyde Park, NY
- Job Description Coordinates and monitors research trials; actively oversees the recruitment of study participants. May b...
- 4/22/2024 12:00:00 AM
Senior Clinical Research Coordinator
- Us Tech Solutions
-
Elizabeth, NJ
- Duration: 12 months contract, Full-Time Employment Type: W-2 Job Description: The Senior Clinical Research Coordinator (...
- 4/20/2024 12:00:00 AM
About Newark, New Jersey
Newark (/ˈnjuːərk/,[24] locally /njʊərk/)[25] is the most populous city in the U.S. state of New Jersey and the seat of Essex County.[26] As one of the nation's major air, shipping, and rail hubs, the city had a population of 285,154 in 2017, making it the nation's 70th-most populous municipality, after being ranked 63rd in the nation in 2000.
Settled in 1666 by Puritans from New Haven Colony, Newark is one of the oldest cities in the United States. Its location at the mouth of the Passaic River (where it flows into Newark Bay) has made the city's waterfront an integral part of the Port of New...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$67,893 to $91,545
Newark, New Jersey area prices
were up 1.6% from a year ago
were up 1.6% 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