Since its inception QPS has been assisting pharmaceutical biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology DMPK Toxicology Bioanalysis Translational Medicine Early Stage Clinical and Phase I IV Clinical Research services. We welcome individuals who want to be part of our growing organization. QPS is an innovative dynamic organization that strives to employ talented caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity innovation and accountability. Employees are encouraged to take responsibility and achieve their best both as individuals and as team members.
Description:
The Data Entry Specialist performs duties within the functions of the Data Entry Department including the maintenance of study related documents the timely reporting of clinical data to clients and/or regulatory authorities. The Data Entry Specialist must possess strong time management skills in order to effectively compile and manage documents perform data entry QC documents participate in client interaction and requests and perform short term or long-term projects as required by the department manager and/or department supervisor within contractual timelines.
Responsibilities:
Develop a full understanding of Standard Operating Procedures study protocols and data entry guidelines for multiple clinical trials and effectively organize study specific information for efficient recall.
Perform all department tasks within pre-defined contractual timelines and according to Standard Operating Procedures study protocols and data entry guidelines.
Compile and interpret data gathered from clinical trials in order to accurately transcribe the data into paper or electronic case report forms.
100 % review of all source documents and case report forms in order to analyze identify query and resolve data issues and inconsistencies ensuring quality reporting standards are met through an established Quality Control process.
Customer service including effective communication with other staff and/or clients regarding client visit preparation client requests and assisting with the completion of both internal and external queries in a timely manner.
Audit the contents of all source document folders after trial completion to ensure completeness and accuracy assisting with resolution of any issues prior to archiving the study files.
Source document organization management and filing.
Qualifications:
Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbents success in this role such as:
High School diploma or equivalent
Previous data management and Microsoft Office experience desired (at least 6 months)
Good time management organizational and interpersonal skills
Good written and oral communication
Ability to work independently and as a team
Consistency in delivering positive results following through with tasks from start to finish
Duties may include more than what is listed and are subject to change without prior notice. Physical requirements for all responsibilities may/do include bending lifting of papers and files prolonged sitting and use of stairs
QPS is an equal opportunity accordance with anti-discrimination law it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race color religion sex sexual orientation gender identity or expression pregnancy age national origin disability status genetic information protected veteran status or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.
Required Experience:
IC
Since its inception QPS has been assisting pharmaceutical biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology DMPK Toxicology Bioanalysis Translational Medicine Early Stage Clinical and Phase I IV Clinical Research services. W...
Since its inception QPS has been assisting pharmaceutical biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology DMPK Toxicology Bioanalysis Translational Medicine Early Stage Clinical and Phase I IV Clinical Research services. We welcome individuals who want to be part of our growing organization. QPS is an innovative dynamic organization that strives to employ talented caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity innovation and accountability. Employees are encouraged to take responsibility and achieve their best both as individuals and as team members.
Description:
The Data Entry Specialist performs duties within the functions of the Data Entry Department including the maintenance of study related documents the timely reporting of clinical data to clients and/or regulatory authorities. The Data Entry Specialist must possess strong time management skills in order to effectively compile and manage documents perform data entry QC documents participate in client interaction and requests and perform short term or long-term projects as required by the department manager and/or department supervisor within contractual timelines.
Responsibilities:
Develop a full understanding of Standard Operating Procedures study protocols and data entry guidelines for multiple clinical trials and effectively organize study specific information for efficient recall.
Perform all department tasks within pre-defined contractual timelines and according to Standard Operating Procedures study protocols and data entry guidelines.
Compile and interpret data gathered from clinical trials in order to accurately transcribe the data into paper or electronic case report forms.
100 % review of all source documents and case report forms in order to analyze identify query and resolve data issues and inconsistencies ensuring quality reporting standards are met through an established Quality Control process.
Customer service including effective communication with other staff and/or clients regarding client visit preparation client requests and assisting with the completion of both internal and external queries in a timely manner.
Audit the contents of all source document folders after trial completion to ensure completeness and accuracy assisting with resolution of any issues prior to archiving the study files.
Source document organization management and filing.
Qualifications:
Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbents success in this role such as:
High School diploma or equivalent
Previous data management and Microsoft Office experience desired (at least 6 months)
Good time management organizational and interpersonal skills
Good written and oral communication
Ability to work independently and as a team
Consistency in delivering positive results following through with tasks from start to finish
Duties may include more than what is listed and are subject to change without prior notice. Physical requirements for all responsibilities may/do include bending lifting of papers and files prolonged sitting and use of stairs
QPS is an equal opportunity accordance with anti-discrimination law it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race color religion sex sexual orientation gender identity or expression pregnancy age national origin disability status genetic information protected veteran status or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.
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