Research Study Coordinator jobs in Jersey City, NJ

Recently Added Research Study Coordinator jobs

D
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
    Experience:
    • 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
    Credentials:
    • ACRP or equivalent certification is preferred
    Knowledge and Skills:
    • 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.
  • 4 Days Ago
Apply this Job
C
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...
  • 1 Month Ago
Apply this Job
S
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
Apply this Job
S
Elementary ELA Tutor
  • Study Evolution Edtech
  • Newark, NJ FULL_TIME
  • Join ClassUp, the premiere online tutoring platform that connects K12 students with our tutors from the top US Universities and Colleges. As a tutor for ClassUp, you will have a flexible schedule and ...
  • 3 Days Ago
Apply this Job
R
Research Coordinator-Stroke Center-Full Time, Day
  • RWJBarnabas Health
  • Livingston, NJ FULL_TIME
  • JOB SUMMARY:The Research Coordinator in Stroke Center is responsible for initiating, coordinating and managing research studies conducted.Other Duties:Please note this job description is not designed ...
  • 15 Days Ago
Apply this Job
5
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...
  • 28 Days Ago
Apply this Job
View All Research Study Coordinator Jobs
Salary Company Skills Job Openings
Filters

Clear All
  • Filter Jobs by companies
  • More
Salary Company Skills Job Openings

0 Research Study Coordinator jobs found in Jersey City, NJ area

F
Pharmacy Technician
  • Frontage Lab
  • Secaucus, NJ
  • Pharmacy Technician Company: Frontage Labs., Inc. Division/Department: Reports to: Pharmacy Supervisor Full-time/ Part-t...
  • 4/27/2024 12:00:00 AM
Apply this job
R
Nuclear Medicine Technologist
  • RWJ Barnabas
  • Jersey City, NJ
  • Job Overview: Performs a wide spectrum of both diagnostic and therapeutic nuclear medicine procedures that require the s...
  • 4/27/2024 12:00:00 AM
Apply this job
C
Big Data Engineer
  • Citigroup, Inc.
  • Jersey City, NJ
  • About Citi Citi, the leading global bank, has approximately 200 million customer accounts and does business in more than...
  • 4/26/2024 12:00:00 AM
Apply this job
C
Sr. Full Stack Engineer (NICE CXone Studio)
  • City National Bank
  • Jersey City, NJ
  • **SENIOR FULL STACK ENGINEER** **WHAT IS THE OPPORTUNITY?** As a member of the Digital Technologies Group, the Full Stac...
  • 4/26/2024 12:00:00 AM
Apply this job
C
Senior Full Stack Engineer
  • City National Bank
  • Jersey City, NJ
  • **SENIOR** **FULL STACK ENGINEER** **WHAT IS THE OPPORTUNITY?** As a member of the Operations Technologies Group, the Fu...
  • 4/26/2024 12:00:00 AM
Apply this job
H
ESL Tutor (In-Person) (PT)
  • Hudson County Community College
  • Jersey City, NJ
  • For COVID-related Information and Vaccination Requirements, please view the Return to Campus Task Force page. College Ov...
  • 4/26/2024 12:00:00 AM
Apply this job
O
Director, Pharmacometrics and Biopharmaceutics Lead - REMOTE
  • Organon & Co
  • Jersey City, NJ
  • Job Description The Position The Director, Pharmacometrics & Biopharmaceutics Lead is responsible for devising the progr...
  • 4/25/2024 12:00:00 AM
Apply this job
O
Director, Pharmacometrics and Biopharmaceutics Lead - REMOTE
  • Organon
  • Jersey City, NJ
  • Job Description The Position The Director, Pharmacometrics & Biopharmaceutics Lead is responsible for devising the progr...
  • 4/24/2024 12:00:00 AM
Apply this job
View All Research Study Coordinator Jobs

About Jersey City, New Jersey

Jersey City is the second most populous city in the U.S. state of New Jersey, after Newark.[29] It is the seat of Hudson County as well as the county's largest city.[30] As of 2017, the Census Bureau's Population Estimates Program calculated that Jersey City's population was 270,753,[22] with the largest population increase of any municipality in New Jersey since 2010,[31] an increase of about 9.4% from the 2010 United States Census, when the city's population was at 247,597.[21][32] ranking the city the 75th-most-populous in the nation.[33] Part of the New York metropolitan area, Jersey City ...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Research Study Coordinator jobs
$70,176 to $94,624
Jersey City, New Jersey area prices
were up 1.6% from a year ago
View detail