Clinical Research Coordinator II

4 days ago


Houston, Texas, United States DM Clinical Research Full time
Job Description

Clinical Research Coordinator II

The Clinical Research Coordinator II will be responsible for ensuring the successful execution of clinical trials at assigned investigative sites. This role will involve ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines, as well as providing high-quality data to sponsors.

Key Responsibilities:

  • Study Execution: Conduct study subject visits, complete protocol-required procedures, and document these in a timely manner.
  • Documentation and Data Management: Adhere to ALCOA-C standards, complete data entry, and resolve queries in a timely manner.
  • Communication and Collaboration: Liaise with laboratory teams, data teams, administrative staff, clinical investigators, research participants, and sponsor/CRO representatives.
  • Administrative Tasks: Submit required administrative paperwork, participate in subject recruitment and retention efforts, and engage with research participants.

Requirements:

  • Education: High School Diploma or equivalent required; Bachelor's degree a plus; Foreign Medical Graduates preferred.
  • Experience: At least one year 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 preferred; Registered Medical Assistant certification or equivalent preferred.

Preferred Qualifications:

  • Language Skills: Bilingual in Spanish preferred.
  • Skills: Energetic, goal-driven, detail-oriented, and able to multi-task.


  • Houston, Texas, United States DM Clinical Research Full time

    Job OverviewThe Clinical Training Coordinator II (Travel) is pivotal in ensuring that high-quality research is executed at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. This role is dedicated to enhancing the performance and skills of the research staff through effective training programs....


  • Houston, Texas, United States DM Clinical Research Full time

    Job OverviewThe Clinical Training Coordinator II (Travel) is responsible for ensuring that high-quality research is conducted at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. This role is pivotal in delivering superior quality data to sponsors and enhancing the performance and skills of site staff...


  • Houston, Texas, United States DM Clinical Research Full time

    Job OverviewThe Clinical Training Coordinator II (Travel) plays a crucial role in ensuring that high-quality research is conducted at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. This position is essential for delivering superior quality data to sponsors and enhancing the performance and skills of...


  • Houston, Texas, United States Houston Methodist Academic Institute Full time

    Position OverviewAt Houston Methodist, the Clinical Research Coordinator II role is pivotal in managing the daily operations of research protocols while evaluating and determining patient eligibility for various research studies.With minimal oversight, this position ensures precise data collection, thorough documentation, and the safety of research...


  • Houston, Texas, United States UTHealth Full time

    Do you want to be a part of a team that can influence the direction of neurocognitive disorders? Full-time, nonexempt role available with our Neurosciences Neurocognitive Disorders Center (NCDC) clinical research team Responsibilities: The Research Coordinator II will work independently, with minimal supervision, to manage investigator-initiated clinical...


  • Houston, Texas, United States Houston Methodist Full time

    Clinical Research Specialist II - Oncology Trials At Houston Methodist, the Clinical Research Specialist II role is pivotal in orchestrating the daily operations of clinical research protocols while evaluating and determining patient eligibility for various studies. This position operates with a degree of autonomy, ensuring precise data collection,...


  • Houston, Texas, United States DM Clinical Research Full time

    Job OverviewPosition Summary:A Study Manager plays a crucial role in ensuring that high-quality research is executed at designated investigative sites, adhering to sponsor protocols, FDA regulations, and ICH/GCP guidelines. The objective is to deliver the highest quality data to the sponsor while meeting or exceeding enrollment expectations and achieving...


  • Houston, Texas, United States Houston Methodist Full time

    Position OverviewAt Houston Methodist, the Clinical Research Coordinator role is pivotal in assisting various initiatives under the guidance of the Clinical Trial Manager. This includes the management of clinical research protocols, collection of patient data as outlined in study protocols, and preparation of study reports.This role is essential in ensuring...


  • Houston, Texas, United States MD Anderson Cancer Center Full time

    OVERVIEWThe University of Texas M. D. Anderson Cancer Center is dedicated to the mission of eradicating cancer through exceptional programs that merge patient care, research, and prevention, alongside educational initiatives for students, professionals, and the community.POSITION SUMMARYThe primary role of the Clinical Research Coordinator is to oversee the...


  • Houston, Texas, United States Houston Methodist Full time

    At Houston Methodist, the Clinical Research Coordinator role is pivotal in assisting various projects under the guidance of the Clinical Trial Manager. This includes the implementation of clinical research protocols, collecting patient data as outlined in the study protocol, and compiling study reports. This position is essential in ensuring precise data...


  • Houston, Texas, United States EVOLUTION RESEARCH GROUP Full time

    About the RoleWe are seeking a highly skilled and detail-oriented Clinical Research Assistant to join our team at Evolution Research Group. As a Clinical Research Assistant, you will play a critical role in the conduct of clinical trials, ensuring the highest level of quality and compliance with regulatory requirements.Key ResponsibilitiesSubject Care and...


  • Houston, Texas, United States Evolution Research Group Full time

    Position: Clinical Research Paramedic Company Overview: Evolution Research Group (ERG) is a prominent independent clinical research organization in the United States, specializing in both early and late-stage neuroscience drug development. With a network of clinical sites, ERG is dedicated to conducting comprehensive phase I-IV clinical research studies,...


  • Houston, Texas, United States DM Clinical Research Full time

    Job OverviewPosition Title: Study ManagerA Study Manager plays a crucial role in ensuring that high-quality research is conducted at designated investigative sites, adhering to the sponsor's protocol, FDA Regulations, and ICH/GCP guidelines. The objective is to deliver the highest quality data to the sponsor while ensuring that study enrollment meets or...


  • Houston, Texas, United States University of Texas MD Anderson Cancer Center Full time

    Coordinator, Clinical Research Program - GI Medical OncologyMission Statement The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through education for undergraduate and graduate students, trainees,...


  • Houston, Texas, United States Houston Methodist Academic Institute Full time

    Position Overview:At Houston Methodist, the Clinical Research Coordinator I plays a pivotal role in managing the daily operations of research protocols while evaluating and determining patient eligibility for various research studies.This role is essential in ensuring precise data collection, thorough documentation, and the safety of all research...


  • Houston, Texas, United States CHI Saint Luke's Hospital at the Vintage Full time

    Position OverviewCHI Saint Luke's Hospital at the Vintage is a distinguished institution recognized for its commitment to innovative research and clinical excellence. Our facility is dedicated to pioneering advancements in various medical fields, including cardiovascular care, neuroscience, oncology, and transplantation.Our dedicated team has established...


  • Houston, Texas, United States Houston Methodist Academic Institute Full time

    Job SummaryHouston Methodist Academic Institute is seeking a highly skilled Research Coordinator I to join our team. The successful candidate will be responsible for coordinating the day-to-day activities of research protocols, ensuring accurate data collection, documentation, and safety of research participants.Key ResponsibilitiesProtocol...


  • Houston, Texas, United States MD Anderson Cancer Center Full time

    The Clinical Research Coordinator plays a pivotal role in collaborating with the research team and principal investigator to oversee research protocols, ensuring adherence to guidelines, maintaining quality assurance, and facilitating communication among staff regarding protocol details. Key Responsibilities Develops, executes, monitors, and reports on...


  • Houston, Texas, United States Pinnacle Clinical Research, LLC Full time

    Job SummaryPinnacle Clinical Research, LLC is seeking a highly skilled and organized Administrative Assistant to provide support to our senior leadership team. As a key member of our team, you will be responsible for ensuring the effective use of senior leadership's time and facilitating productive interactions with staff and key stakeholders.Key...


  • Houston, Texas, United States aQua Dialysis Full time

    Job OverviewKEY RESPONSIBILITIES INCLUDE:· Evaluate potential participants for eligibility in clinical trials and effectively communicate trial details.· Facilitate the informed consent process and ensure patient enrollment in accordance with protocols.· Oversee patient care while adhering to protocol specifications.· Collaborate with physicians to...