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Working Towards Quality Medical Care for the Future

Careers

Become a part of the Quality Clinical Research team

Join Our Team

Quality Clinical Research is seeking a highly motivated and individual to join the research operations group as a Clinical Research Coordinator. The coordinator will play a key role in coordinating all clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include GCP proficiency, logical thinking, ability to prioritize, can-do attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.

The Coordinator, working closely with study team members under the moderate direction of a Study Investigator, will have overall responsibilities for coordinating efforts with other study team members in order to achieve study objectives and corporate goals, including:

  • Develop strong working relationships and maintain effective communication with study team members.
  • Track key study metrics using tracking tools (creating and maintaining documents, tables, databases, spreadsheets, and files), providing timely and quality updates to management.
  • Adhere to an IRB approved protocol.
  • Coordinate protocol related research procedures, study visits, and follow-care.
  • Maintain study source documents. Report adverse events.
  • Educate subjects protocol, study intervention, study drug, etc.
  • Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities.
  • Advertise, and conduct telephone screening to recruit potential subjects.
  • Phlebotomy, Injections, ECG

QUALIFICATIONS AND EDUCATION REQUIREMENTS

  • Former Combat Medics, LPN, Paramedics. MA, Pharmacy Tech
  • Requires experience in phlebotomy and injections
  • Strong interpersonal skills with attention to detail a must. Demonstrated ability in positive relationship building, with strong verbal and written skills required.
  • Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
  • Ability to travel for Clinic activities, attend investigator meetings or vendor visits/audits, as required
  • Must be flexible with their schedule, and willing to work one weekend day every month.

Excellent attendance history and punctuality is a must

Email resume to Seneca@qcromaha.com

Quality Clinical Research is seeking a highly motivated and individual to join the research operations group as a Regulatory Specialist. The regulatory specialist will play a key role in maintaining all required documentation for all clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include GCP proficiency, logical thinking, ability to prioritize, can-do attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.

The regulatory specialist, working closely with study team members under the moderate direction of a Study Investigator, will have overall responsibilities for completion and maintenance off all study documents in order to achieve study objectives and corporate goals, and GCP and FDA compliance

  • Develop strong working relationships and maintain effective communication with study team members.
  • Prepare all study start up documents
  • Maintain and file all study documents during the study
  • Submit to the IRB
  • Coordinate protocol related research procedures, study visits, and follow-care.
  • Advertise, and conduct telephone screening to recruit potential subjects.

QUALIFICATIONS AND EDUCATION REQUIREMENTS

  • Strong interpersonal skills with attention to detail a must. Demonstrated ability in positive relationship building, with strong verbal and written skills required.
  • Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
  • Excellent attendance history and punctuality is a must.

Email resume to Seneca@qcromaha.com

Quality Clinical Research is seeking a highly motivated individual to join the research operations group as a Clinical Research Assistant. The clinical research assistant will play a key role in coordinating all clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include GCP proficiency, logical thinking, ability to prioritize, can-do attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.

The Research Assistant, working closely with study team members under the moderate direction of a Study Investigator, with responsibilities to support clinical research coordinators in conducting clinical trials from pre-study planning through successful completion of all subject visits and documentation.

DUTIES AND RESPONSIBILITIES
● Responsible for the collection, processing, and shipment of laboratory samples in accordance with site, protocol, laboratory and Good Clinical Practice (GCP) specifications.
● Obtain vital signs, perform ECGs and other clinical procedures according to the site, protocol, and Good Clinical Practice (GCP) specifications.
● Perform administrative duties and other duties as needed.
● Develop knowledge about how procedures are conducted in compliance with the clinical protocol and enhance clinical research knowledge.
● Comply with Good Clinical Practices (GCPs) at all times.
● Behave in a cooperative and constructive manner
● Perform other duties as assigned or needed.

QUALIFICATIONS AND EDUCATION REQUIREMENTS

  • Former Combat Medics, LPN, Paramedics. MA, Pharmacy Tech
  • Lab processing experience
    ● Experience as a phlebotomist and able to administer injection
  • Must be flexible with their schedule, and willing to work one weekend day every month.
  • Excellent attendance history and punctuality is a must.

Email resume to Seneca@qcromaha.com

Quality Clinical Research is seeking a highly motivated and individual to join the Research Operations group as a Lab Technician. The lab technician will play a key role in processing all specimens in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include GCP proficiency, logical thinking, ability to prioritize, can-do attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.

The lab technician, working closely with study team members under the moderate direction of a Study Investigator, with responsibilities to processing and shipment of all urine, stool and blood specimens, perform vitals, ECG, phlebotomy and injections.

DUTIES AND RESPONSIBILITIES

  • Typical tasks include receiving patients for office visits, taking their vital signs, administering injections, phlebotomy, processing lab samples
  • reviewing medical records, ordering medical supplies, etc.
  • Processing all specimen samples
  • Shipment of IATA specimen samples

 

QUALIFICATIONS AND EDUCATION REQUIREMENTS

  • Former Combat Medics, LPN, Paramedics. MA, Pharmacy Tech
  • Lab processing experience
    ● Experience as a phlebotomist and able to administer injection
  • A candidate with strong writing and computer skills is a must. Grammar and speaking skills must be above average.
  • Lab processing experience will be a plus
  • Must be flexible with their schedule, and willing to work one weekend day every month.
  • Excellent attendance history and punctuality is a must.

Email resume to Seneca@qcromaha.com

The Research Recruiter will be responsible for recruiting best-in-class candidates for openings that span multiple levels of research studies in Omaha Nebraska. The successful Recruiter will be considered a trusted advisor and strategic partner and work closely with recruiting eligible patients for currently enrolling studies.

Our Recruiter must have extensive experience working with outside sales representatives, particularly in the medical or pharmacological industries. The successful candidate will have a keen eye when reviewing protocol criteria and conducting patient interviews. If you’re sharp, professional and sales-oriented, we would like to speak with you about this opportunity.

DUTIES AND RESPONSIBILITIES

  • Develop creative sourcing strategies for hard to fill studies including direct sourcing, internet recruiting, networking, utilization of external research, etc. Proactively create a talent pipeline of patients.
  • Responsible for recruiting subject for all current enrolling studies. This includes, but not limited to, phone screening, radio, television, newspaper and other printed advertising
  • Increase patient flow and develop strategic sourcing solutions that will attract and acquire highly qualified patients.
  • Support full-life cycle recruitment needs including direct sourcing techniques, and consultative skills, and adhere to best clinical practice principles.
  • Develop a detailed understanding and awareness of each research area and its organization in order to improve the quality and alignment of recruitment support with the needs of the area.
  • Responsible to define and implement a standard and consistent process, define service guidelines and metrics as needed.
  • Responsible for developing phone screening form per protocol specifics.
  • Will be on call to speak with potential subjects and schedule appointments for screening visits.
  • Assist with all literature and equipment needed for health expo’s
  • Participate in health fairs to recruit subjects for clinical trials
  • Complete all paperwork associated with recruitment
  • Organize and maintain all records required for recruitment for all clinical research studies
  • Attend Clinical Research startup meetings when required
  • Establish a working relationship with the Clinical Research Coordinator’s

QUALIFICATIONS

  • 1 or more year(s) of recruitment experience
  • Ability to prioritize and work on multiple projects at a time.
  • Strong written and verbal communication skills.
  • Must have experience working with Excel, PowerPoint, and social media/networking sites.
  • In-depth knowledge of the pharmaceutical industry is desired from concept to pre-clinical.
  • Excellent interpersonal and communication skills

Email resume to Seneca@qcromaha.com

Quality Clinical Research is always looking for qualified Investigators to join our team.  QCR brings together expert physicians who share a passion for clinical research. Our team is comprised of forward-thinking professionals who execute phase I- IV clinical trials with the highest regard for patient safety and data quality. Quality Clinical Research’s culture allows for continuous collaboration between Investigator teams and sponsor.
DUTIES AND RESPONSIBILITES

  • Serving as an investigator (Principal Investigator or Sub-Investigator)
  • Conducting informed consent process
  • Evaluating potential participants for inclusion/exclusion criteria
  • Reviewing medical history
  • Reviewing laboratory results
  • Conducting study assessments
  • Overseeing all aspects of the clinical study

Contact Seneca at Seneca@qcromaha.com to learn more