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Director Antimicrobial Resistance Jobs (NOW HIRING)

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Monitor and synthesize the scientific literature in clinical microbiology, antimicrobial resistance ... g., medical director, clinical microbiologist) or in a scientific/medical affairs role at a ...

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Director Antimicrobial Resistance information

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How much do director antimicrobial resistance jobs pay per year?

As of Aug 10, 2026, the average yearly pay for director antimicrobial resistance in the United States is $186,382.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,500.00 and $249,500.00 per year, depending on experience, location, and employer.
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What cities are hiring for Director Antimicrobial Resistance jobs? Cities with the most Director Antimicrobial Resistance job openings:
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Infographic showing various Director Antimicrobial Resistance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $186,382 per year, or $89.6 per hour.

Microbiologist II Antimicrobial Resistance

nLeague

Indianapolis, IN • On-site

Contractor

Re-posted just now


Job description

Job ID: 804995             

Position: Microbiologist II Antimicrobial Resistance

Client: IDOH

Location: 550 W 16th St Ste B, Marion County, Indianapolis, IN 46202

Duration:6 + Months

  • This position is part of the Indiana Department of Health Laboratory, Antimicrobial Resistance Lab Network.’

Purpose of Position/Summary:

  • Incumbent is responsible for coordinating and performing the full range of microbiological examinations and analyses including culture, biochemical tests, PCR, and WGS of clinical specimens for isolation and identification of bacteria and yeast including but not limited to E.coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumanii, and Candida auris.
  • Incumbent will also be responsible for the documentation of all quality control and quality assurance activities according to CLIA regulations.
  • In addition, this position may cross-train in other areas of the lab that may include molecular, microbiological, viral, serological, and other techniques to support routine testing and provide backup capacity.
     

Essential Duties/Responsibilities:

  • Incumbent will have in-depth knowledge and ability in the area of microbiology and molecular biology and is able to perform laboratory associated assays or the ability to learn these techniques upon successful completion of proficiency testing.  Representative duties include:
  • Conducting examinations of samples and/or reference samples for analyses such as but not limited to, molecular detection or isolation and identification of microorganisms or their nucleic acids.
  • Strictly follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results.
  • Extraction of nucleic acids from specimens, isolates, and samples via a variety of manual and automated methods;
  • Utilize molecular techniques such as, but not limited to, PCR, sequencing, MALDI-TOF, and WGS;
     Evaluate, interpret, and validate laboratory results and reports findings.
  • Maintain laboratory record system of submitted samples and specimens and their possible referral.
  • Conduct quality control checks on laboratory methods, materials, and equipment in strict adherence to the laboratory's quality control policies.
  • Maintain an inventory of laboratory supplies and order as needed to ensure testing needs are met.
    Assist in preparations of epidemiological and/or statistical reports from data compiled on a daily, weekly, monthly, or annual basis.
  • Maintain competency in all trained areas.
  • Perform all related work as required.
  • Testing personnel responsibilities (493.1495 Standard):
  • The testing personnel are responsible for specimen processing, test performance and for reporting test results.
        (a)    Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill       commensurate with the individual’s education, training or experience, and technical abilities.
        (b)    Each individual performing high complexity testing must—
            (1)    Follow the laboratory’s procedures for specimen handling and
                processing, test analyses, reporting and maintaining records of patient
                test results;
            (2)    Maintain records that demonstrate that proficiency testing samples are
                tested in the same manner as patient specimens;
            (3)    Adhere to the laboratory’s quality control policies, document all quality
                control activities, instrument and procedural calibrations and
                maintenance performed;
            (4)    Follow the laboratory’s established policies and procedures whenever
                test systems are not within the laboratory’s established acceptable levels
                of performance;
            (5)    Be capable of identifying problems that may adversely affect test
                performance or reporting of test results and either must correct the
                problems or immediately notify the general supervisor, technical
                supervisor, clinical consultant, or director;
            (6)    Document all corrective actions taken when test systems deviate from
                the laboratory’s established performance specifications; and
            (7)    Except as specified in paragraph (c) of this section, if qualified under §
                493.1489(b)(5), perform high complexity testing only under the onsite,
                direct supervision of a general supervisor qualified under § 493.1461.
        (c)    Exception. For individuals qualified under § 493.1489(b)(5), who were performing
            high complexity testing on or before January 19, 1993, the requirements of
            paragraph (b)(7) of this section are not effective, provided that all high complexity
            testing performed by the individual in the absence of a general supervisor is
            reviewed within 24 hours by a general supervisor qualified under § 493.1461.
    Job Requirements:
  • Extensive knowledge of the principles, theories and practices of microbiology and related sub- specialties;
  • Specialized knowledge of current scientific methods and testing procedures and the ability to apply them when seeking solutions to public health laboratory problems;
  • Specialized knowledge of and ability to use a full range of standard technical equipment, complex scientific apparatus, and automated techniques of analysis;
  • Extensive knowledge of laboratory safety practices and principles;
  • Aware of state and federal laws, rules, regulations, and policies concerning the program area (i.e. CLIA);
  • Ability to meet requirements for personnel certification as a technologist pursuant to the Clinical Laboratory Improvement Act (CLIA)
  • Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships;
  • Ability to satisfactorily participate in proficiency testing programs and recognize QA problems;
  • Ability to compile, analyze, evaluate, and prepare laboratory reports.