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Research Assistant-MORL Genetics
$65k-87k (estimate)
Full Time | Ambulatory Healthcare Services 4 Months Ago
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The University of Iowa is Hiring a Research Assistant-MORL Genetics Near Iowa, IA

University of Iowa Health Care Department of Otolaryngology is seeking a Research Assistant to perform clinical molecular diagnostic testing in the area of genetic hearing loss and rare complement-mediated renal disease.. The Research Assistant (RA) will work with whole blood, saliva and DNA samples received into the Molecular Otolaryngology and Renal Research Laboratories – Clinical Diagnostics Services (MORL CDS). The RA will perform sample accessioning, DNA extraction and quantification, perform PCR, Sanger sequencing and MLPA testing, develop primers, perform next generation sequencing (NGS), evaluate genetic variants using computation methods, report results, maintain inventory and quality management for the CDS. Key areas of responsibilities include conducting clinical and research activities/experiments, collecting, analyzing, and summarizing data, preparing reports, contributing to manuscripts/publications, administrative and project management, facilities and equipment management, and supervision/staffing. Specifically, these responsibilities will apply within the setting of a renal and hearing clinical and research laboratory molecular biology methodologies.

KEY AREAS OF RESPONSIBILITY

Research:

Track information in MS Word and Excel spreadsheets for clinical and research purposes.

Perform data entry and correction on source documents and into electronic data capture system.

Prepare progress reports and provide support for the genetic CDS team.

Perform clinical laboratory activities based upon protocols developed by other staff or principal investigator.

Read and review articles as directed.

As individual skills develop, develop and validate genetic tests including investigation of genes, development of assays and evaluation of screening techniques.

Experiments, Investigations, Evaluations:

Read and understand protocols.

Perform a variety of assays and experimental tests involving PCR, sanger sequencing, and MLPA (multiplex ligation-dependent probe amplification).

Perform molecular biology techniques including RT-PCR, DNA extraction and quantification, and gel electrophoresis.

Perform next generation sequencing (NGS)

Calibrate and operate laboratory equipment including thermocyclers, centrifuges, and spectrophotometers.

Perform and meet proficiency and competency testing standards and maintain data and equipment records according to regulatory guidelines.

Develop primers, amplimer, and protocol optimization.

Arrange and plan daily activities to coordinate with genetic CDS team members to meet weekly deadlines.

Perform procedures assuring fidelity to protocols.

Perform varied tasks in the clinical laboratory.

Adhere to safety and compliance guidelines.

Collect, record and consolidate data as directed by the Principal Investigator.

Track progress of clinical laboratory activities.

Adhere to Quality Assurance protocols to maintain validity and integrity of the data.

As individual skills develop: troubleshoot, analyze and propose modifications to protocols; perform complex techniques per protocol; test and evaluate current procedures; develop and implement procedures for monitoring data integrity; present results at team meetings.

Collect, Analyze and Summarize Data; Prepare Reports; Contribute to Manuscripts, Publications:

Collect and track, perform data entry for reports and maintain records of methods used.

Prepare materials for reports.

As skills develop, analyze data.

Evaluate data to establish relevance to the problem or problems being evaluated.

Prepare bibliographies and abstracts for publications and may present results/finding at team, departmental and national meetings.

Administrative and Project Management:

Assist in tracking various indicators of project progress.

Assist in documenting compliance with safety and regulatory guidelines.

Provide public contact and customer service to physicians and genetic counselors requesting MORL genetic screening services.

Adhere to safety and compliance guidelines.

Facilities and Equipment Management:

Assist in the preparation, calibration, and maintenance of laboratory and facility equipment.

Assist with procurement of supplies and materials.

May initiate purchasing requests.

Supervision/Staffing:

As skills develop, may train, provide direction, assignments, feedback, coaching and counseling of employees to assure outcomes are achieved.

As skills develop, instruct assistants in laboratory procedures and techniques; requisition supplies and materials.

UNIVERSAL COMPETENCIES

Ability to work with a variety of individuals and groups in a constructive and civil manner while appreciating the unique contribution of individuals from varied cultures, race, creed, color, national origin, age, sex, disability, sexual orientation, and gender identity.

Ability to utilize existing resources and learning to achieve or exceed desired outcomes of current and future organizational goals/needs. Able to demonstrate ethical behavior in diverse situations while producing results.

Ability to meet or exceed customer service needs and expectations and provide excellent service in a direct or indirect manner. Ability to effectively transmit and interpret information through appropriate communication with internal and external customers.

JOB FAMILY TECHNICAL COMPETENCIES

Knowledge of formal methodologies, tools and techniques for conducting research, studies and tests.

Knowledge of and the ability to locate, interpret and evaluate research findings compiled and documented by others and use this material to support empirical research.

Knowledge of and ability to utilize tools and techniques for producing well-written, meaningful and usable documentation of research findings.

Knowledge of practices, behaviors, applicable laws, rules, and regulations governing proper research conduct; ability to demonstrate ethical and compliant behavior in diverse situations.

Knowledge of the procedures and programs in place in the organization to ensure employee, student and subject safety (occupational safety, fire, patient, animal, drug, radiation, environmental safety and emergency plans); ability to train others; ability to take appropriate actions in case of emergency.

SUPERVISION RECEIVED

Supervision is received from a designated official.

SUPERVISION EXERCISED

Functional supervision may be exercised over undergraduate students.

Required Qualifications

  • A Bachelor’s degree or an equivalent combination of education and experience. Preference: Microbiology, Biology, Genetics or Similar
  • Experience with molecular biology techniques including PCR, DNA extraction and quantification, and gel electrophoresis
  • Experience managing large data sets and maintaining highly organized and detailed research records.
  • Excellent organizational, interpersonal, and communication (both verbal and written) skills
  • Willingness to learn relevant lab protocols under supervision of the principal investigator and other staff
  • Proficiency in computer software applications, including Microsoft Office Suite
  • Ability to analyze information and situations, prioritize tasks, develop solutions to challenges
  • Ability to use good judgment while working independently and in a team setting

Desirable Qualifications

  • Experience evaluating genetic variants for significance using computational methods
  • Experience developing primers, amplimer validation and protocol development
  • Experience preparing solutions and purchasing supplies
  • Understanding of clinical testing conduct as outlined in a testing protocol is desirable.
  • Demonstrated ability to resolve issues related to customer concerns or workflow changes and challenges.

Successful candidates will be subject to a criminal background check and education/credential verification. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check. Up to 5 professional references will be requested at a later step in the recruitment process.

In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission:

  • Resume
  • Cover Letter

Job openings are posted for a minimum of 14 calendar days and may be removed from posting and filled any time after the original posting period has ended.

For additional questions, please contact Lydia Messer at lydia-messer@uiowa.edu

Benefits Highlights

  • Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
  • The University of Iowa offers a generous benefits package, including paid vacation and paid sick leave. Complete information regarding the full benefits package may be viewed at: Benefits | University Human Resources - The University of Iowa (uiowa.edu)

Applicant Resource Center –

Need help submitting an application or accepting an offer? Support is available!

Our Applicant Resource Center is now open in the Fountain Lobby at the Main Hospital.

Hours:

Tuesdays & Thursdays 2:00pm – 4:00pm

Or by appointment

Contact TAHealthCareSupport@healthcare.uiowa.edu to schedule a time to visit.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Ambulatory Healthcare Services

SALARY

$65k-87k (estimate)

POST DATE

05/21/2023

EXPIRATION DATE

08/22/2024

WEBSITE

uiowa.edu

HEADQUARTERS

COUNCIL BLUFFS, IA

SIZE

7,500 - 15,000

FOUNDED

1847

TYPE

Private

CEO

KRISTA SMITH

REVENUE

$3B - $5B

INDUSTRY

Ambulatory Healthcare Services

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