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Southgate Medical Group, LLP

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Clinical Research Study Coordinator

West Seneca, NY · On-site

$54K - $84K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Clinical Research Study Coordinator to work as part of our research team. We provide 401k with match, free skin center services, scrubs, generous paid time off, 6 paid holidays ...

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How much do medical research study jobs pay per year?

As of Aug 12, 2026, the average yearly pay for medical research study in the United States is $53,326.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $58,000.00 per year, depending on experience, location, and employer.
Infographic showing various Medical Research Study job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.

Research Study Coordinator 1-Research Center (Knoxville)

The University of Tennessee

Knoxville, TN • On-site

$21.69/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description


Market Range: 08
Hiring Range: $21.69/Hourly
Under the direction of the GSM Director of Research, the Research Study Coordinator 1 performs as the Research Study Coordinator for Investigator-Initiated Cancer Research. This position assists the faculty with clinical research study activities including but not limited to the development, submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, and preparation and maintenance of study files and essential trial documents.
Responsibilities
  1. Assists investigators with the development of design studies by reviewing and/or writing proposals to determine best-suited methods for study objectives.
  2. Assists investigators with the collection and submission process for initial Institutional Review Board (IRB) submissions including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, Investigational New Drug (IND) information, Drug(s)/Device(s) specifics, and IRB application completion and upload into iMedRIS.
  3. Assists investigator with the IRB Continuing Review process that includes the completion of study status reports.
  4. Prepares study-specific protocols, source documents/spreadsheets, drafts of required study logs and essential trial documents, and prepares files.
  5. Assists investigator with the execution and coordination of GSM Investigator-Initiated Cancer Research.
  6. Assists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication lists, obtaining informed consent from patients, coordinating study visits and procedures to be completed on campus, collecting study data, and performing study assessments if needed (lab draws, questionnaires, vital signs, etc.) for Investigator-Initiated Studies.
  7. Establishes and maintains contact with study participants and families, community agencies, and health care providers.
  8. Assists investigator with the management and maintenance of Subject Source Documents.
  9. Identifies funding opportunities and assists with reviewing and/or writing grant proposals.
  10. Performs other duties assigned

Qualifications
EDUCATION: Bachelor's Degree in relevant health field. (TRANSCRIPT REQUIRED)
EXPERIENCE: One (1) year of relevant experience; OR Associate's Degree and three (3) years of relevant experience, OR an equivalent combination of education, training, and experience to equal five (5) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
  • Ability to create and maintain extensive medical records on clinical research subjects.
  • Understanding of hospital policies and procedures, medical records and documentation, and HIPAA regulations.
  • Knowledge of research protocol with an understanding of Basic Research Principles and Federal Code of Regulations for Clinical Research Studies.
  • Ability to manage multiple priorities.
  • Ability to interact with a diverse population.
  • Intermediate-level computer skills with the ability to learn new software applications for various electronic data capture programs.
  • Ability to exhibit strong interpersonal and communication skills.

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