We have other current jobs related to this field that you can find below

  • Clinical Research Coordinator III

    2 months ago

    Irving, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinical Research Coordinator IIIA 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...

  • Clinical Research Coordinator Assistant

    5 days ago

    Irving, Texas, United States NEXT Oncology Full time

    Position Overview:As a vital member of the NEXT Oncology team, the Clinical Research Coordinator Assistant plays a crucial role in supporting patients throughout their clinical journey. This position is designed to assist patients by managing referral appointments and ensuring seamless communication between various stakeholders involved in clinical...

  • Sr. Clinical Research Coordinator

    3 days ago

    Irving, United States Kelly Services Full time

    Kelly Science & Clinical® is working with a Clinical Research Site Network with an immediate need for an experienced Clinical Research Coordinator with site leadership experience for the Dallas Metro area.  Position: Clinical Research Coordinator III (Full-Time/Non-Exempt): On-Site Responsible for the overall management the studies assigned to you...

  • Clinical Pharmacy Specialist II

    6 days ago

    Irving, Texas, United States CHRISTUS Health Full time

    Position Overview: In this clinical capacity, the Clinical Pharmacy Specialist II plays a vital role in the medication management system, delivering tailored pharmaceutical care to patients within designated areas. Key Responsibilities: Provide comprehensive pharmaceutical care services, which encompass evaluating patient requirements, integrating age and...

  • Clinical Research Project Associate

    6 days ago

    Irving, Texas, United States Medpace Full time

    Position Overview:Medpace, a prominent Contract Research Organization (CRO) dedicated to supporting Biotech firms, is on the lookout for individuals with advanced degrees (PhDs or Post-Doctoral experience) to fill the role of Clinical Research Project Associate (CRPA). This full-time, office-based position is integral to our Clinical Trial Management...

  • Clinical Study Recruiter

    5 days ago

    Irving, Texas, United States ALLIANCE CLINICAL LLC Full time

    Job OverviewSUMMARY: The Clinical Study Recruiter plays a crucial role in expanding our research participant database by identifying and evaluating potential candidates for clinical trials. This position demands exceptional communication skills to effectively engage with individuals from diverse backgrounds.KEY RESPONSIBILITIES: The following duties are...

  • Clinical Study Recruiter

    6 days ago

    Irving, Texas, United States ALLIANCE CLINICAL LLC Full time

    Job OverviewSUMMARY: The Clinical Study Recruiter plays a vital role in enhancing our research database by identifying and evaluating potential participants for clinical trials. This role demands exceptional communication skills, enabling effective interaction with individuals from diverse backgrounds.KEY RESPONSIBILITIES: The following duties are essential...

  • Central Services Coordinator JR

    1 month ago

    Irving, United States ALLIANCE CLINICAL LLC Full time

    Job DescriptionJob DescriptionESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Comply with all company policies, procedures, and conduct.Strictly adhere to confidentiality and compliance standards.Virtually communicate effectively and courteously with study patients via tele-health platform.Demonstrate a caring and...

  • Clinical Informatics Systems Analyst II

    2 days ago

    Irving, Texas, United States Christus Health Full time

    About the Role:We are seeking a highly skilled Clinical Informatics Systems Analyst II to join our team at Christus Health. This position involves supporting the operation and administration of clinical information systems, collaborating with both clinical and technical colleagues to enhance workflow processes and tools.Key Responsibilities:Collaborate with...

  • Regulatory Affairs Coordinator II

    5 days ago

    Irving, Texas, United States Christus Health Full time

    Overview:In this role, you will serve as the key regulatory liaison for researchers and team members. Your primary duties will involve facilitating the flow of information and supporting researchers in the development of Institutional Review Board (IRB) submissions. You will oversee the preparation of applications for review by the IRBs and will...

  • Information Services Developer II

    2 months ago

    Irving, United States Catapult Staffing Full time

    Information Services Developer II Department: Information Services Location: Irving, TX Role Type: Full-time About Our Client Our client is a forward-thinking organization in the information services sector, leveraging cutting-edge technology to deliver innovative solutions. With a strong focus on customer service and technological advancement, the...

  • Clinical Pharmacy Specialist II

    6 days ago

    Irving, Texas, United States CHRISTUS Health Full time

    Overview:The Clinical Pharmacy Specialist is entrusted with the responsibility of ensuring the safe, effective, and timely administration of medication therapy. In this role, Clinical Pharmacy Specialists deliver expert patient-focused care within a decentralized healthcare environment. They engage in all critical components of the medication-use process...

  • Clinical Pharmacy Specialist II

    5 days ago

    Irving, Texas, United States CHRISTUS Health Full time

    Job Description Description Overview: The Clinical Pharmacy Specialist is entrusted with ensuring the safe, effective, and timely administration of medication therapies. In this role, Clinical Pharmacy Specialists deliver expert patient-centered care within a decentralized clinical environment. They engage in all essential components of the medication-use...

  • Accountant II

    2 months ago

    Irving, United States Talencia LLC Full time

    Job DescriptionJob DescriptionPosition: Accountant II- OnsiteBachelors Degree in Accounting is required Shift: Mon-Fri - 8am to 5pmDuration: 3 MonthsCST Local candidates onlyPay:USD $31.03/hrFacility: Christus System OfficeAddress: 5101 N. O\'Connor Blvd, Irving TX 75039SummaryThe Accountant II is responsible for preparing general ledger month-end...

  • Clinical Trial Navigator

    1 month ago

    Irving, United States NEXT Oncology Full time

    Position Description: POSITION SUMMARY:Under the direction and supervision of the Research Coordinator Manager, this position is responsible assisting patients by coordinating referral appointments. The CTN performs general clerical tasks such as answering phone calls and emails, maintains patient records, and verifies insurance information. The position...

  • Registered Nurse Care Coordinator

    5 days ago

    Irving, Texas, United States Christus Health Full time

    Position Overview: RN Care Manager IIAs a dedicated and empathetic RN, you have the opportunity to significantly impact patient health outcomes. In the role of RN Care Manager II, you will collaborate with physicians and a diverse healthcare team to create and execute tailored care strategies for each patient, ensuring they achieve optimal health results.Key...

  • Clinical Review Nurse II

    5 days ago

    Irving, Texas, United States Impresiv Health Full time

    Título: Clinical Review Nurse IIDescripción: El Clinical Review Nurse II es responsable de evaluar la adecuación clínica de la atención brindada a los pacientes y asegurar la utilización adecuada de los recursos hospitalarios. Este profesional de enfermería se encarga de realizar una variedad de revisiones y funciones relacionadas con la gestión de...

  • Financial Analyst II

    5 days ago

    Irving, Texas, United States Sigma Full time

    Financial Analyst II Sigma Inc is seeking a Financial Analyst II to contribute to our finance team. Work Schedule: Monday - Friday, 8 AM to 5 PM Position OverviewThis role is accountable for comprehensive financial reporting related to Client Health Information Management, Clinical Engineering, and TechSource.A solid grasp and extensive knowledge of...

  • Registered Nurse Care Coordinator

    5 days ago

    Irving, Texas, United States Christus Health Full time

    Position Overview: RN Care Manager IIAs a dedicated and empathetic RN, you have the opportunity to significantly impact patient health outcomes. In the role of RN Care Manager II, you will collaborate with a team of healthcare professionals to design and execute tailored care strategies for each patient, ensuring they receive the highest quality of care....

  • Registered Nurse Care Coordinator

    4 hours ago

    Irving, Texas, United States Christus Health Full time

    Position Overview: RN Care Manager IIAs a dedicated and experienced RN, you will play a vital role in enhancing patient care within our organization. In the capacity of RN Care Manager II, you will collaborate with healthcare providers and a diverse team to craft and execute tailored care strategies for each patient, ensuring they achieve optimal health...

Clinical Research Coordinator II

2 months ago

Irving, United States DM Clinical Research Full time
Job DescriptionJob Description

Clinic Research Coordinator II
 
The Clinical Research Coordinator II, will ensure that quality research is conducted at the 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. The CRC I will also 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:
    • a. Sponsor-provided and IRB-approved Protocol Training
    • b. All relevant Protocol Amendments Training
    • c. Any study-specific Manuals Training, as applicable
    • d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting 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 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 and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
  • Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
  • Submitting required administrative paperwork per company timelines.
  • Participating in subject recruitment and retention efforts.
  • Engaging with Research Participants and understanding their concerns.
  • Any other matters, as assigned by management.

Knowledge & Experience:

Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a plus
  • Foreign Medical Graduates preferred 
Experience:
  • At least one years of experience as a CRC,  preferably with practice coordinating industry-sponsored vaccines in a private setting.
  • At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting
Credentials:
  • ACRP or equivalent certification is preferred 
  • Registered Medical Assistant certification or equivalent  is preferred 
  • Knowledge and Skills:
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Bilingual in Spanish is preferred

Powered by JazzHR

MIIma2WIZt