Clinical Research Coordinator jobs in Oklahoma

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)

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Clinical Research Coordinator
  • EmVenio Research
  • Oklahoma, OK FULL_TIME
  • ABOUT EMVENIO RESEARCH:

    EmVenio Research delivers localized trial access to diverse and underserved communities. We empower patients and embrace communities on their terms. Our research solutions cultivate a sustainable local ecosystem that benefits all stakeholders. Removing barriers and unlocking doors to innovation reduces risk and time associated with clinical research, while improving ROI.

    EmVenio Research offers competitive pay, a comprehensive benefits program and opportunities for learning and career development. We promote a diverse and inclusive workplace, and our team members have a voice in their work through surveys and town halls.

    POSITION SUMMARY:
    As a Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations site teams at one or multiple of our permanent community Mobile Research Units (MRU), or occasionally through home visits management. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. The CRC is responsible for ensuring participant safety, data integrity, data quality, and maintenance of protocol standards in various therapeutic areas. As a CRC, you will assist various virtual Principal Investigators (vPIs), through delegated authority, with conducting clinical trials per federal, state, and institutional guidelines, while learning the responsibilities during all phases of trials from pre-study implementation through study closure. This role is all encompassing to ensure efficient study conduct and site procedures from a remote position.

    ESSENTIAL FUNCTIONS
    Reasonable Accommodations Statement
    To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
     
    Essential Functions:

    • Study coordination:
      • Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
      • Maintains CTMS, eISF, participant scheduling management, QC, and review.
      • Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).
      • Helps ensure that all study related activities are complete including returning supplies, returning unused stock of study drug/devices, and confirming that all queries are complete.
    • Data management:
      • Ensures timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects.
      • Follows ALCOA C good documentation practices.
    • Remote monitoring:
      • Conduct remote monitoring activities to ensure compliance with study protocols and regulatory requirements, with full patient documentation available.
      • Address and resolve issues identified during remote monitoring visits.
      • Perform clinical duties (e.g. drug preparation and administration, phlebotomy, ECG, lab processing) within scope or delegation if and when on-site.
    • Regulatory Compliance:
      • Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
      • Reviews new protocols and other materials provided by study sponsors and gives input to the Principal Investigators (PIs), site leadership, and site staff, as applicable, regarding study conduct and research issues in order to resolve financial and clinical feasibility.
      • Assists in conducting quality checks and audits of research studies to check the accuracy, integrity, and consistency of the research studies.
      • Maintains compliance with OSHA HIPPA, GCP and ICH.
    • Communication and Collaboration:
      • Works collaboratively with internal and external stakeholders such as physicians, nurse practitioners, physician assistants, clinical research specialists, leaders, family members, key care givers and any ancillary medical personnel as appropriate.
      • Performs other duties as assigned including but limited to recruitment, and community engagement activities, which may occur after hours and/or on weekends.
      • Coordinates team conference calls and distribution of meeting minutes.
    • Training and Support:
      • Ensure staff are delegated, trained appropriately and documented.
      • Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
      • Support sites with daily temperature monitoring and inventory management.
      • Regular and reliable attendance with the ability to work after hours/weekends as needed as well as rotating on-call shifts that may include weeknights, weekends, and holidays. 

    Supervisory Responsibilities:
    • None.

    POSITION QUALIFICATIONS

    SKILLS AND ABILITIES
    Education:  Associate or Bachelor’s degree or equivalent experience.

    Experience:  At least two (2) years or more of recent clinical research experience required. Two (2) years of experience performing phlebotomy, subcutaneous injections, collecting vital signs, ECG, and urine collection preferred.

    Computer Skills:  Excellent computer Skills, including Microsoft Office.

    Certificates & Licenses:  Current BLS, CITI, GCP, and IATA preferred.

    Other Requirements:
    • Excellent verbal and written communication.
    • Use of considerable judgment/critical thinking in application of procedures, practices, and policies to work problems, organization, and administration of research or outpatient clinic.
    • Working knowledge of federal, state, and local laws and regulations governing research.
    • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
    • Ability to provide patient-centric focus.
    • Adaptability/flexibility to react positively to changes in work environment. Initiative to improve productivity and quality of work.
    • Experience collecting, processing, and shipping lab specimen(s).
    • Ability to plan and organize work in logical and efficient manner.
    • Ability to manage time delicate projects to meet deadlines.
    • Strong attention to detail.
    • Excellent ability to establish and maintain effective working relationships.
    • Prolonged periods of sitting at a desk and working on a computer.
    • Prolonged periods of standing, bending, and reaching.
    • Must be able to lift up to 50 pounds at times.
    • Have the ability to travel regionally by car or nationally by plane, a valid state driver license, proof of adequate automobile insurance coverage for the state of residence.


    WORK ENVIRONMENT
    Work is performed primarily in a mobile clinical environment, and the incumbent may be exposed to body fluids and infectious diseases. The noise level in the work environment is usually quiet in office settings and moderate in other situations. There is potential that you may be exposed to infectious diseases including but not limited to: Influenza, COVID-19, RSV, etc. Each clinician is equipped with proper PPE and/or supplies to ensure their safety when handling such potential subjects and/or samples.

    The preceding functions may not be comprehensive in scope regarding work performed by an employee assigned to this position classification.  Management reserves the right to add, modify, change or rescind the work assignments of this position.  Management also reserves the right to make reasonable accommodations so that a qualified employee(s) can perform the essential functions of the position.
     

    Location1301 N Portland Ave, Oklahoma City, OK 73107 (potential of some remote work) 

    Amount of Travel Required: up to 10%

    Schedule: Monday – Friday 8am - 4:30pm, may vary

    Compensation: $60,000 - $80,000. The actual rate offered will carefully consider a wide range of factors, including your skills, qualifications, experience, and location.

  • Just Posted

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Clinical Research Coordinator - Temp to Hire
  • Delricht Research
  • Tulsa, OK FULL_TIME
  • Why DelRicht Research? Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a posi...
  • 19 Days Ago

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Clinical Research Coordinator - Experienced Clinician
  • Delricht Research
  • Tulsa, OK FULL_TIME
  • Why DelRicht Research? Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a posi...
  • 1 Month Ago

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Clinical Research Coordinator
  • Rivus Wellness and Research Institute
  • Oklahoma, OK FULL_TIME
  • Rivus Wellness and Research Institute is growing and we are looking for individuals who are passionate about delivering exceptional patient care. In this position, you will be responsible for the over...
  • 1 Month Ago

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Clinical Research Coordinator
  • Actalent
  • Tulsa, OK OTHER
  • Description:This position will help identify patients for enrollment through chart review, patient follow-up and pre-screening. This individual will be speaking with potential patients over the phone ...
  • 4 Days Ago

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Limited Term Clinical Research Injector
  • Delricht Research
  • Tulsa, OK TEMPORARY
  • Why DelRicht Research? Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a posi...
  • 4 Days Ago

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Clinical Research Coordinator
  • Apex Systems
  • Burlingame, CA
  • Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. This role will work with ...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Danbury Health Systems
  • Poughkeepsie, NY
  • Full Time Clinical Research Coordinator Opportunity - Poughkeepsie, NY (75 Miles from New York City) Nuvance Health has ...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Sanford Health
  • Fargo, ND
  • Create Your Career With Us! Sanford Health is one of the largest and fastest-growing not-for-profit health systems in th...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Mayo Clinic Health System
  • Rochester, MN
  • Why Mayo Clinic Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & Worl...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Methodist Healthcare
  • San Antonio, TX
  • Description Introduction Are you looking for a work environment where diversity and inclusion thrive? Submit your applic...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • University of Miami Miller School of Medicine
  • Miami, FL
  • Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click he...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Beth Israel Lahey Health
  • Boston, MA
  • When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. Job Typ...
  • 3/27/2024 12:00:00 AM

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Clinical Research Coordinator
  • CARLE
  • Peoria, IL
  • Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
  • 3/26/2024 12:00:00 AM

Oklahoma is the 20th-largest state in the United States, covering an area of 69,899 square miles (181,040 km2), with 68,595 square miles (177,660 km2) of land and 1,304 square miles (3,380 km2) of water. It lies partly in the Great Plains near the geographical center of the 48 contiguous states. It is bounded on the east by Arkansas and Missouri, on the north by Kansas, on the northwest by Colorado, on the far west by New Mexico, and on the south and near-west by Texas. Much of its border with Texas lies along the Southern Oklahoma Aulacogen, a failed continental rift. The geologic figure defi...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$55,555 to $74,895

Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019