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


  • Dallas, United States Wake Research Full time

    Job DescriptionJob DescriptionCompany DescriptionM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the...


  • Dallas, United States TEN20Clinical Trials Full time

    Company Description We suggest you enter details here. Role Description This is a full-time on-site role as a Clinical Trial Coordinator located in Dallas, TX. The Clinical Trial Coordinator will be responsible for coordinating and managing all aspects of clinical trials, including participant recruitment, data collection and analysis, documentation, and...


  • Dallas, United States TEN20Clinical Trials Full time

    Company Description We suggest you enter details here. Role Description This is a full-time on-site role as a Clinical Trial Coordinator located in Dallas, TX. The Clinical Trial Coordinator will be responsible for coordinating and managing all aspects of clinical trials, including participant recruitment, data collection and analysis, documentation, and...


  • dallas, United States TEN20Clinical Trials Full time

    Company Description We suggest you enter details here. Role Description This is a full-time on-site role as a Clinical Trial Coordinator located in Dallas, TX. The Clinical Trial Coordinator will be responsible for coordinating and managing all aspects of clinical trials, including participant recruitment, data collection and analysis, documentation, and...


  • Dallas, United States DALLAS VA RESEARCH CORPORATION Full time

    Job DescriptionJob DescriptionEducation and Experience Requirements: Must be eligible to work in the U.S.; H1b visa holders are ineligible More than 4 years of research experience; or 3+ years of research experience and a Bachelor Degree in a relevant area; or 3+ years of research experience and an LVN; or Greater than 1 year of research experience and a...


  • Dallas, Texas, United States ALLIANCE CLINICAL LLC Full time

    Position OverviewJob Summary: The Clinical Research Assistant plays a crucial role in supporting clinical studies by ensuring compliance with protocols and maintaining high standards of patient interaction.Key Responsibilities:1) Adhere to all organizational policies and ethical guidelines.2) Maintain strict confidentiality and compliance with regulatory...


  • Dallas, Texas, United States TEN20Clinical Trials Full time

    Job SummaryTEN20Clinical Trials is seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team. As a Clinical Trial Coordinator, you will be responsible for coordinating and managing all aspects of clinical trials, including participant recruitment, data collection and analysis, documentation, and compliance with regulatory...


  • Dallas, United States Baylor Scott & White Health Full time

    JOB SUMMARYThe Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementation through study closure per federal, state and Institutional guidelines. This position will learn to assist Principal Investigators on more complex...


  • Dallas, United States Baylor Scott White Health Full time

    JOB DESCRIPTION Shift: 8AM-5PM Mon-Fri in office Location: Baylor University Medical Center, 3500 Gaston Ave Dallas, TX Department: Trauma Research Center JOB SUMMARY This position will be part of a research team focused on the psychological experiences of a variety of medical conditions including those admitted to critical care...


  • Dallas, United States Baylor Scott & White Healthcare Full time

    JOB SUMMARY Regulatory Affairs Specialist provides regulatory guidance, monitoring and administrative help to the Institutional Review Board, Institutional Animal Care and Use Committee and Data and Safety Monitoring Board and other people involved in the conduct of research at all Baylor Scott & White Health ESSENTIAL FUNCTIONS OF THE ROLEReview all IRB...


  • Dallas, Texas, United States TEN20Clinical Trials Full time

    About TEN20Clinical TrialsTEN20Clinical Trials is a leading provider of clinical research services, dedicated to delivering high-quality results in a timely and cost-effective manner.Job SummaryWe are seeking a highly motivated and organized Clinical Trial Coordinator to join our team. The successful candidate will be responsible for coordinating and...


  • Dallas, Texas, United States Wake Research Full time

    Job OverviewThe Clinical Trial Coordinator (CTC) is a dedicated research professional who collaborates closely with the clinical research site management and the Principal Investigator (PI). While the PI holds the primary responsibility for the overall execution of the clinical trial, the CTC oversees, supports, facilitates, and organizes the daily...


  • Dallas, Texas, United States Baylor Scott & White Healthcare Full time

    Clinical Research Operations ManagerOverview: This role entails the daily oversight of flow cytometry core operations and personnel. The successful candidate will possess extensive knowledge and practical experience in flow cytometry sample handling, specimen evaluation, and cell sorting under BSL2+ conditions, coupled with exceptional leadership and...


  • Dallas, United States WILLIAM R LUMRY MD PA Full time

    Job DescriptionJob DescriptionSeeking experienced Clinical Research Coordinator to assist with ongoing clinical trials in the asthma and allergy space. Experience witn regulatory, patient recruitment and assessment, electronic data capture and conduct of clinical trial required.Company DescriptionWe are a Allergy & Immunology office, we study allergies, low...


  • Dallas, Texas, United States University of Texas Southwestern Medical Center Full time

    Clinical Research Nurse - Magnet Program and Research Department Why University of Texas Southwestern Medical Center?With a legacy of over 75 years in the Dallas-Fort Worth area, the University of Texas Southwestern Medical Center is dedicated to excellence, innovation, collaboration, and compassion. We prioritize your growth by offering career advancement...


  • Dallas, Texas, United States ALLIANCE CLINICAL LLC Full time

    Position OverviewJob Summary: The Clinical Research Assistant plays a vital role in the execution of clinical trials, ensuring adherence to protocols and regulatory standards.Key Responsibilities:1) Uphold all organizational policies and ethical standards.2) Maintain strict confidentiality and compliance with all regulations.3) Engage effectively and...


  • Dallas, Texas, United States ALLIANCE CLINICAL LLC Full time

    Job OverviewPosition Summary: The Clinical Research Assistant plays a crucial role in supporting clinical trials and ensuring compliance with study protocols.Key Responsibilities:1) Adhere to all organizational policies and ethical standards.2) Maintain confidentiality and compliance with regulations.3) Engage professionally with study participants.4) Gather...


  • Dallas, United States Clinitiative Health Research Full time

    Clinitiative Health Research is a pioneering force in the clinical trial industry. Based in the United States with a global reach, we are at the forefront of connecting top-tier pharmaceutical companies and Clinical Research Organizations (CROs) with the most distinguished principal investigators and clinical research sites. Our mission is to significantly...


  • Dallas, 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.Communicate effectively and courteously with study patients.Collect patient medical history and conditions.Obtain...


  • Dallas, United States Wake Research Full time

    Job DescriptionJob DescriptionCompany DescriptionM3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake...

Submission for the position: Clinical Research Coordinator

3 months ago


Dallas, United States Baylor Scott & White Healthcare Full time
JOB SUMMARY

The Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementation through study closure per federal, state and Institutional guidelines. This position will learn to assist Principal Investigators on more complex studies and seek guidance from more senior roles when needed.

ESSENTIAL FUNCTIONS OF THE ROLE

  • Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors.
  • Creates, facilitates, and/or executes a variety of different project workflows based on the needs of the clinical trial protocol.Examples of workflows include, providing in-service education for healthcare professionals and working with Pharmacy to ensure a smooth project flow.
  • Ensures that appropriate billing or charging mechanisms are in place for research charges related to research studies. Requires familiarity with research study budgets and provides feedback on budgets for new clinical trials.
  • Performs research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
  • Partners and coordinates with regulatory compliance including preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms. Ensures that all study documents are complete and that records are retained per federal, state and institutional standards.
  • Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.
  • Conducts and coordinates study-monitoring visits. Conducts audits and quality checks of research studies to check the accuracy, integrity and consistency of research studies.
KEY SUCCESS FACTORS
  • Research certification or other certifications per specialty area preferred.
  • Proven written and oral communication skills.
  • Exceptional computer skills, including Microsoft Office.
  • Ability to manage time reactive projects in order to meet deadlines.
  • Exceptional ability to establish and maintain effective working relationships.
BENEFITS

Our competitive benefits package includes the following.
  • Immediate eligibility for health and welfare benefits
  • 401(k) savings plan with dollar-for-dollar match up to 5%
  • Tuition Reimbursement
  • PTO accrual beginning Day 1


Note: Benefits may vary based upon position type and/or level

QUALIFICATIONS

- EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification

- EXPERIENCE - Less than 1 Year of Experience