Clinical Research Technician
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QPS, LLC
Springfield, MO, US
Summary
The Clinical Research Technician monitors study volunteers to ensure compliance with protocols and safety requirements. They are also responsible for recording clinical data, performing vitals, and maintaining the cleanliness of study areas.
Job Description
The Clinical Research Technician position offers flexible hours and a rewarding work environment in the drug research field. This position is primarily responsible for monitoring the study volunteers and ensuring the clinical study is being recorded, conducted, and reported in agreement with the study requirements. This position offers variety, and no two days are alike. The hours are scheduled on an as needed basis and can range from 0-29 hours per week. The essential duties are:
- Read and understand study documents, time and events, study restrictions and expectations of sponsor.
- Check in/out study volunteers and monitor their behavior for study compliance, safety, adverse events and concerns.
- Perform essential study duties such as recording mealtimes, performing vitals and recording results.
- Review raw data to ensure accuracy.
- Help to supervise events to ensure studies are done on time and in accordance with SOPs and Protocols.
- Maintain cleanliness of the clinics and all study-related areas.
Experience
- High school diploma or equivalent
- Outstanding customer service skills
- High attention to detail
- Ability to work weekends is desirable
- Ability to work flexible hours
Please visit Recruitment (adp.com) to apply for this position through the company website.
QPS Bio-Kinetic (BKCA) provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, QPS Bio-Kinetic (BKCA) complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
QPS is a GLP/GCP-compliant contract research organization (CRO) delivering the highest grade of discovery, preclinical, and clinical drug development services. An award-winning leader focused on bioanalytics and clinical trials, QPS is known for proven quality standards, technical expertise, a flexible approach to research, client satisfaction and turnkey laboratories and facilities. We are passionate about our work, creating value for patients and customers while generating opportunities for employees to thrive.
Since 1995, it has rapidly expanded from a tiny bioanalysis shop to a full-service CRO with 1100+ employees in the US, Europe, India and Asia. Today, it offers expanded pharmaceutical contract R&D services with special expertise in Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, and Clinical Development.
Through continual enhancements in capacities and resources, QPS stands tall in its commitment to deliver superior quality, skilled performance and trusted service to its valued customers.
Founded
1995
Company size
1,001-5,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Newark, DE
QPS is a GLP/GCP-compliant contract research organization (CRO) delivering the highest grade of discovery, preclinical, and clinical drug development services. An award-winning leader focused on bioanalytics and clinical trials, QPS is known for proven quality standards, technical expertise, a flexible approach to research, client satisfaction and turnkey laboratories and facilities. We are passionate about our work, creating value for patients and customers while generating opportunities for employees to thrive.
Since 1995, it has rapidly expanded from a tiny bioanalysis shop to a full-service CRO with 1100+ employees in the US, Europe, India and Asia. Today, it offers expanded pharmaceutical contract R&D services with special expertise in Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, and Clinical Development.
Through continual enhancements in capacities and resources, QPS stands tall in its commitment to deliver superior quality, skilled performance and trusted service to its valued customers.
Founded
1995
Company size
1,001-5,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Newark, DE