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University of New Mexico
Albuquerque, NM | Full Time
$255k-418k (estimate)
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University of New Mexico
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Lovelace Biomedical (LBERI)
Albuquerque, NM | Full Time
$54k-72k (estimate)
3 Days Ago
Lovelace Biomedical (LBERI)
Albuquerque, NM | Full Time
$54k-72k (estimate)
3 Days Ago
University of New Mexico
Albuquerque, NM | Full Time
$56k-74k (estimate)
3 Months Ago
University of New Mexico
Albuquerque, NM | Full Time
$56k-74k (estimate)
3 Months Ago
Lovelace Biomedical Research Institute
Albuquerque, NM | Full Time
$56k-74k (estimate)
4 Months Ago
University of New Mexico
Albuquerque, NM | Full Time
$64k-85k (estimate)
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University of New Mexico
Albuquerque, NM | Full Time
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DM Clinical Research
Albuquerque, NM | Full Time
$56k-74k (estimate)
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University of New Mexico
Albuquerque, NM | Full Time
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University of New Mexico
Albuquerque, NM | Full Time
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unm
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unm
Albuquerque, NM | Full Time
$52k-69k (estimate)
3 Months Ago
Research Coordinator
$54k-72k (estimate)
Full Time | Business Services 3 Days Ago
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Lovelace Biomedical (LBERI) is Hiring a Research Coordinator Near Albuquerque, NM

Overview
  • The Research Coordinator will work with a research team on several federally-funded studies designed to evaluate the behavioral and physiological effects of nicotine and tobacco use in human research participants, as well as other studies as needed. Responsibilities include:
    • Oversees, organizes, and executes daily activities for research studies including the recruitment, screening, and scheduling of study participants.
    • Administers research questionnaires and assessments.
    • Performs blood and urine specimen collection and processing.
    • Performs data collection, analysis and interpretation in order to ensure data integrity, quality control and protocol compliance. Manages data and tracking of participants.
    • Reviews and comprehends each research protocol including study procedures and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections.
    • Coordinates with PI to help ensure that clinical research and related activities are performed consistently with the organization’s standard procedures and applicable regulations.
    • Utilizes established physiological, psychological, socio-behavioral and/or neurobiological research methods, techniques and procedures in performing research.
    • Ensures proper compliance with Institutional Review Board (IRB) and other regulatory agencies to include: preparation and maintenance of regulatory binder information and all IRB correspondence with regards to study submissions.
    • Maintains research records in a confidential manner according to organizational policies, sponsor confidentiality agreements, human subjects protection regulations, and other applicable regulations.
    • Maintains research participant screening logs and protocol deviation logs.
    • Assists with study materials such as informed consent documents, recruitment materials, case report forms, test article logs, and enrollment logs.
    • Orders and maintains research supplies, compiles research charts, prepares source documents, and related duties.
    • Organizes data for the preparation of project progress reporting and for proposals for new funding.
    • Contributes to the design of current and upcoming research projects using scientific approaches and methodologies.
    • Assists in the planning of data presentations, preparation of papers for publication, presentations and conferences and in the writing of project reports, articles and other documents. Provides analytic and narrative input for abstracts, manuscripts and presentations.
    • Performs other related duties as assigned.
QualificationsRequires a bachelor’s degree in a scientific discipline or related field and a minimum of 2 years of directly-related expertise in human/clinical research studies; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained.
The Research Coordinator position requires specialized knowledge and comprehensive research, administrative, organizational, and operational skills, along with experience in a clinical research setting.
Must have a sound and fundamental knowledge of federal and state laws and regulations pertaining to human subject research.
Requires a professional demeanor, strong analytical, time management, and organizational skills, meticulous attention to detail, and excellent verbal/written communication and interpersonal skills.
Must have demonstrated success in working independently as well as a part of a team, and the ability to work against firm deadlines.
Must have professional-level computer skills and advanced experience with Microsoft Office and Google systems and the ability to learn department-specific computer systems as needed.
Preferred/Additional Qualifications
  • Knowledge of FDA and OHRP regulations and guidance as well as training in research ethics, HIPAA, and GCP are preferred.
  • Experience with REDCap is preferred
  • Expertise in scientific protocol and consent form writing/editing, as well as working with IRBs for protocol management across the study lifecycle are preferred.
  • CCRP, CCRC, or similar clinical research certification is strongly preferred. If applicant does not have a current clinical research certification, applicant must meet requirements to apply for certification upon hire, and obtain the certification (at company's cost) within a year.
Physical RequirementsWork is performed in a dry laboratory environment. Will operate standard office equipment and will frequently stand, walk, sit, perform desk-based computer tasks, use a telephone, perform repetitive motions and occasionally lift objects that weigh up to 20 pounds. May interact with research participants.
The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position.
Salary Salary is commensurate with experience.
EEO, including disability/vets

Job Summary

JOB TYPE

Full Time

INDUSTRY

Business Services

SALARY

$54k-72k (estimate)

POST DATE

06/27/2024

EXPIRATION DATE

07/25/2024

WEBSITE

lovelacebiomedical.org

HEADQUARTERS

Albuquerque, NM

SIZE

50 - 100

INDUSTRY

Business Services

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The job skills required for Research Coordinator include Clinical Research, Presentation, Data Collection, Planning, Scheduling, HIPAA, etc. Having related job skills and expertise will give you an advantage when applying to be a Research Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Research Coordinator. Select any job title you are interested in and start to search job requirements.

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The following is the career advancement route for Research Coordinator positions, which can be used as a reference in future career path planning. As a Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Research Coordinator. You can explore the career advancement for a Research Coordinator below and select your interested title to get hiring information.

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If you are interested in becoming a Research Coordinator, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Research Coordinator for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Research Coordinator job description and responsibilities

Research coordinator administers clinical trials under following good clinical practice guidelines.

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These coordinators work at clinical research sites where they will study their subjects to ensure the successful operation of the clinical trial.

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Research coordinators (CRC) prepare, direct, and coordinate clinical trail projects.

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Research coordinators would also collaborate with other representatives that offer equipment or software for the trial to ensure all requirements are met.

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Research coordinators carefully organize clinical studies to produce the most accurate results possible.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Research Coordinator jobs

Learn about current research programs.

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Research up-to-date guidelines and regulations.

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Research Coordinators guide their subjects through every aspect of the trials and distribute questionnaires after the study to help researchers gauge their viability.

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Familiarity with scientific research standards and practices.

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Research coordinator also performs various administrative tasks required for whichever study they are currently administrating.

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