Pharmacy Tech for Clinical Research
Job descriptionJob OverviewCoordinate and execute activities related to the Investigational Product (IP).
Participate in clinical research studies ensuring that clinical trial tasks are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential FunctionsoProvides clinical research support to investigators to prepare for and execute all tasks related to the investigational productoReviews study protocols and study documents and instructions related to the investigational productoComplete all required sponsor trainingoFollow and maintain all blinding procedures with study volunteers and blinded team membersoEnsure appropriate receipts of all investigational productoMaintains source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principlesoMaintain responsibility for the management of inventory/IP accountability:
i.
e.
, orders, replacements, return of IP study materialsoRecord and maintain appropriate temperature of the IP per study protocoloPreparation and administration of IP to clinical research patientsoCorresponds with research subjects to troubleshoot study-related questions or concernsoParticipates in routine meetings with site study staff and Investigators to confirm study tasks are assigned and are executed to the expected standardsoActively involved in study data quality checking and query resolutionoUpdates and maintains site staff skills, training and knowledge of current best nursing practices and topics related to clinical researchoAssists the investigators to safeguard the well-being of subjects and maintain standards required of clinical research sitesoMaintains a safe environment in accordance with site policiesoReports any deviations from normal research practices to senior staff and implement agreed changes in the study care programoAssists investigator in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standardsoAssists in providing training to new investigator site staff members on study-specific topics and requirementsoProvides guidance and supervision to lower-level site staff to help provide that processes are carried out in line with protocols and SOP's, where applicableoParticipates in study process reviews and enhancement efforts to support control of site unit budget, development of the research facilities and site services and the culture towards a high performing research study teamoPrepares for and attend study monitoring visits, study audits and regulatory inspections with clinical research regulatory agenciesoAdheres to standard operating procedures (SOPs) and other directives throughout this processoAssists research site with coverage planning related to staffing and scheduling for research projectsQualificationsoCurrent, clean Pharmacy Technician License in applicable stateo2
years Pharmacy Technician experience o2
years' experience administering vaccines oExcellent patient care experience oBasic knowledge of medical terminologyoProficient in the use of technologyoAbility to work independently, prioritize actively, seek input, problem solve and work in a team environment.
oAbility to maintain confidentiality.
oAbility to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
Learn more athttps:
//jobs.
iqvia.
comWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
https:
//jobs.
iqvia.
com/eoe />As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status.
https:
//jobs.
iqvia.
com/covid-19-vaccine-status />Colorado/California/Washington state Pay Transparency :
The salary range for this role is $64,300 - $80,400.
The actual salary will vary based on factors like candidate qualifications and competencies.
Certain roles are eligible for annual bonus, sales incentives and/or stock.
Benefits may include healthcare, retirement, paid time off, and more.
Recommended Skills Administration Auditing Clinical Research Clinical Trials Confidentiality Data Quality Estimated Salary: $20 to $28 per hour based on qualifications.
Participate in clinical research studies ensuring that clinical trial tasks are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential FunctionsoProvides clinical research support to investigators to prepare for and execute all tasks related to the investigational productoReviews study protocols and study documents and instructions related to the investigational productoComplete all required sponsor trainingoFollow and maintain all blinding procedures with study volunteers and blinded team membersoEnsure appropriate receipts of all investigational productoMaintains source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principlesoMaintain responsibility for the management of inventory/IP accountability:
i.
e.
, orders, replacements, return of IP study materialsoRecord and maintain appropriate temperature of the IP per study protocoloPreparation and administration of IP to clinical research patientsoCorresponds with research subjects to troubleshoot study-related questions or concernsoParticipates in routine meetings with site study staff and Investigators to confirm study tasks are assigned and are executed to the expected standardsoActively involved in study data quality checking and query resolutionoUpdates and maintains site staff skills, training and knowledge of current best nursing practices and topics related to clinical researchoAssists the investigators to safeguard the well-being of subjects and maintain standards required of clinical research sitesoMaintains a safe environment in accordance with site policiesoReports any deviations from normal research practices to senior staff and implement agreed changes in the study care programoAssists investigator in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standardsoAssists in providing training to new investigator site staff members on study-specific topics and requirementsoProvides guidance and supervision to lower-level site staff to help provide that processes are carried out in line with protocols and SOP's, where applicableoParticipates in study process reviews and enhancement efforts to support control of site unit budget, development of the research facilities and site services and the culture towards a high performing research study teamoPrepares for and attend study monitoring visits, study audits and regulatory inspections with clinical research regulatory agenciesoAdheres to standard operating procedures (SOPs) and other directives throughout this processoAssists research site with coverage planning related to staffing and scheduling for research projectsQualificationsoCurrent, clean Pharmacy Technician License in applicable stateo2
years Pharmacy Technician experience o2
years' experience administering vaccines oExcellent patient care experience oBasic knowledge of medical terminologyoProficient in the use of technologyoAbility to work independently, prioritize actively, seek input, problem solve and work in a team environment.
oAbility to maintain confidentiality.
oAbility to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
Learn more athttps:
//jobs.
iqvia.
comWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
https:
//jobs.
iqvia.
com/eoe />As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status.
https:
//jobs.
iqvia.
com/covid-19-vaccine-status />Colorado/California/Washington state Pay Transparency :
The salary range for this role is $64,300 - $80,400.
The actual salary will vary based on factors like candidate qualifications and competencies.
Certain roles are eligible for annual bonus, sales incentives and/or stock.
Benefits may include healthcare, retirement, paid time off, and more.
Recommended Skills Administration Auditing Clinical Research Clinical Trials Confidentiality Data Quality Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
