QPS Holdings, LLC Jobs Hiring Now
QPS Holdings, LLC is hiring for 22 open roles on Migrate Mate as of July 16, 2026, concentrated in biotech & life sciences and clinical support, with listed salaries up to about $150,000. Migrate Mate updates QPS Holdings, LLC's live openings daily. QPS Holdings, LLC is a contract research organization that conducts clinical trials and bioanalytical research for pharmaceutical and biotechnology clients.
Find QPS Holdings, LLC JobsOverview
QPS Holdings, LLC hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 22
- Top team
- Biotech & Life Sciences
- Seniority
- Across all levels
- Work type
- 5% remote or hybrid
- Top location
- Miami
- Salary range
- $45,000–$150,000
Listed salaries for QPS Holdings, LLC roles on Migrate Mate range from about $45,000 to $150,000 per year across 22 open roles, as of July 16, 2026. One role lists an hourly contract rate.
Open Roles at QPS Holdings, LLC
Showing 22 of 22+ QPS Holdings, LLC jobs
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 incumbent’s 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
Benefits package:
- Medical, dental, vision, LTD, and life insurance
- Paid holidays
- PTO and sick time
- Bonuses dependent on personal and company success
- Promotion of work/life balance
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 incumbent’s 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
Benefits package:
- Medical, dental, vision, LTD, and life insurance
- Paid holidays
- PTO and sick time
- Bonuses dependent on personal and company success
- Promotion of work/life balance
Job Roles at QPS Holdings, LLC
Working at QPS Holdings, LLC
QPS Holdings, LLC's 22 open roles are across all levels, and about 5% are remote or hybrid. The most active teams are biotech & life sciences, clinical support, and nursing. QPS Holdings, LLC is a contract research organization providing clinical research, bioanalytical laboratory services, and drug development support to pharmaceutical and biotechnology companies. The work spans early-phase clinical trials, data management, pharmacokinetics, and regulatory science across research and operations functions. Most QPS Holdings, LLC roles are based in Miami, with some in Newark and Springfield.
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Browse jobs by roleQPS Holdings, LLC Jobs: Frequently Asked Questions
How many jobs is QPS Holdings, LLC hiring for right now?
QPS Holdings, LLC is hiring for 22 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in biotech & life sciences and clinical support. Roles span clinical operations, laboratory science, data management, and business development functions across multiple research sites.
What kinds of roles does QPS Holdings, LLC hire for?
The most active teams are biotech & life sciences, clinical support, and nursing. QPS Holdings hires across clinical operations, bioanalytical and pharmaceutical science, data management, and administrative support. Sample titles include Clinical Operations Specialist, Associate Scientist, Mass Spectrometry Technician, Clinical Pharmacist, and Research Coordinator. Most postings are across all levels.
Are QPS Holdings, LLC jobs remote or in-person?
Mostly on-site. About 5% of QPS Holdings, LLC's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Miami. Each QPS Holdings, LLC listing shows its work location so you can filter before applying.
How do I apply to a job at QPS Holdings, LLC?
Find a QPS Holdings, LLC role on Migrate Mate and follow the listing through to QPS Holdings' own careers page to submit your application directly. QPS Holdings manages its own hiring process, including screening and interviews. Migrate Mate keeps listings current so the roles shown are actively being filled.
What do QPS Holdings, LLC jobs pay?
Listed salaries for QPS Holdings, LLC roles on Migrate Mate range from about $45,000 to $150,000 per year as of July 16, 2026, with most postings at across all levels. One role lists an hourly contract rate. Exact pay is set by QPS Holdings, LLC and shown on each listing.
Does QPS Holdings, LLC hire entry-level?
Most of QPS Holdings, LLC's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual QPS Holdings, LLC listings for stated experience requirements.
Where is QPS Holdings, LLC hiring?
Most QPS Holdings, LLC roles are based in Miami, with some in Newark and Springfield, and about 5% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.