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Principal Investigator – Clinical Research

9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001 · Springfield, MO, US, Springfield, MO · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
Company9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001
TitlePrincipal Investigator – Clinical Research
Normalized title-
Department / team-
LocationSpringfield, MO, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-05-19 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from 9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Springfield.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001
Source23fd82d9-c7cc-4299-8499-ec8ee9834434
ATS providerADP Workforce Now Recruiting

Description

Principal Investigator - Clinical Trials Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS is seeking an experienced Principal Investigator (PI) to provide senior clinical leadership within its research unit. This role is well suited for a seasoned investigator who enjoys combining hands-on study responsibility with broader clinical oversight, continuity, and mentorship. The PI will lead assigned studies while also serving as a trusted clinical resource and back-up for PRN and Contract PIs, helping ensure consistent study conduct, regulatory compliance, and subject safety across the portfolio. This position is 100% office/lab based at QPS in Springfield, MO and offers meaningful influence over study quality and execution. QPS’ Story: 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 Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings. ________________________________________ Key Responsibilities Lead clinical trials in accordance with ICH-GCP, federal and state regulations, and approved protocols Provide senior clinical oversight and continuity across studies supported by PRN and Contract PIs Serve as back-up PI as needed to support uninterrupted study conduct Ensure subject safety, rights, and confidentiality at all times Oversee and participate in the informed consent process, ensuring clarity, compliance, and documentation integrity Confirm that all subjects meet 100% of inclusion and exclusion criteria prior to dosing Guide, mentor, and provide clinical input to PRN and Contract PIs and study staff Ensure appropriate delegation, training, and maintenance of essential trial documentation Act as a primary point of contact with sponsors, IRBs, monitors, and auditors Participate in investigator meetings, monitoring visits, audits, and inspections ________________________________________ Qualifications MD or DO (Board Certified) Strong working knowledge of ICH-GCP and clinical research regulations Experience leading clinical studies as a PI or Sub-Investigator Endocrinology expertise or therapeutic-area experience helpful Candidates with a strong endocrinology background will be considered even without prior CRO experience Comfortable operating with a high degree of autonomy while collaborating across teams Excellent written and verbal communication skills Proficiency with MS Office and standard clinical research systems Ability to work a flexible schedule, including occasional nights, weekends, and holidays ________________________________________ Why Join QPS This role offers an opportunity to apply deep clinical expertise in a setting that values judgment, continuity, and scientific rigor. You’ll remain directly involved in study conduct while helping shape how trials are executed across the unit—without the administrative weight of formal people management. For experienced PIs, QPS provides a platform to focus on quality, mentorship, and meaningful clinical impact, while working closely with sponsors and multidisciplinary teams in a collaborative, well-supported research environment. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans. #LI-DNI

Full job record

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Source ID23fd82d9-c7cc-4299-8499-ec8ee9834434
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Provider Job Key591375
TitlePrincipal Investigator – Clinical Research
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First Seen At2026-05-31 18:25:14Z
Last Seen At2026-06-06 13:18:39Z
Last Checked At2026-06-06 13:18:39Z
Last Changed At2026-06-06 13:18:39Z
Inactive At—
Source Posted At2026-05-19 15:50:00Z
Source Updated At—
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    "requisitionDescription": "<div><div><div><div><p data-pasted=\"true\"><strong><span style=\"font-size: 14px; font-family: verdana, sans-serif;\">Principal Investigator - Clinical Trials</span></strong></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! &nbsp;</strong></span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">QPS is seeking an experienced <strong>Principal Investigator (PI)&nbsp;</strong>to provide senior clinical leadership within its research unit. This role is well suited for a seasoned investigator who enjoys combining hands-on study responsibility with broader clinical oversight, continuity, and mentorship.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">The PI will lead assigned studies while also serving as a trusted clinical resource and back-up for PRN and Contract PIs, helping ensure consistent study conduct, regulatory compliance, and subject safety across the portfolio. This position is <strong>100% office/lab based at QPS in Springfield, MO</strong> and offers meaningful influence over study quality and execution.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">QPS&rsquo; Story:</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">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 Phase Clinical and Phase II &ndash; IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.&nbsp;</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">________________________________________</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>Key Responsibilities</strong></span></p><ul><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Lead clinical trials in accordance with ICH-GCP, federal and state regulations, and approved protocols</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Provide senior clinical oversight and continuity across studies supported by PRN and Contract PIs</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Serve as back-up PI as needed to support uninterrupted study conduct</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Ensure subject safety, rights, and confidentiality at all times</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Oversee and participate in the informed consent process, ensuring clarity, compliance, and documentation integrity</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Confirm that all subjects meet 100% of inclusion and exclusion criteria prior to dosing</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Guide, mentor, and provide clinical input to PRN and Contract PIs and study staff</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Ensure appropriate delegation, training, and maintenance of essential trial documentation</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Act as a primary point of contact with sponsors, IRBs, monitors, and auditors</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Participate in investigator meetings, monitoring visits, audits, and inspections</li></ul><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">________________________________________</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>Qualifications</strong></span></p><ul><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">MD or DO (Board Certified)</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Strong working knowledge of ICH-GCP and clinical research regulations</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Experience leading clinical studies as a PI or Sub-Investigator</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Endocrinology expertise or therapeutic-area experience helpful<ul style=\"font-family: initial; font-size: initial;\"><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Candidates with a strong endocrinology background will be considered even without prior CRO experience</li></ul></li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Comfortable operating with a high degree of autonomy while collaborating across teams</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Excellent written and verbal communication skills</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Proficiency with MS Office and standard clinical research systems</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Ability to work a flexible schedule, including occasional nights, weekends, and holidays</li></ul><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">________________________________________</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>Why Join QPS</strong></span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">This role offers an opportunity to apply deep clinical expertise in a setting that values judgment, continuity, and scientific rigor. You&rsquo;ll remain directly involved in study conduct while helping shape how trials are executed across the unit&mdash;without the administrative weight of formal people management.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">For experienced PIs, QPS provides a platform to focus on quality, mentorship, and meaningful clinical impact, while working closely with sponsors and multidisciplinary teams in a collaborative, well-supported research environment.</span></p><p style=\"box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; margin: 0in; line-height: 1.25; color: rgb(38, 35, 33); font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; font-size: 15px; font-family: Arial, sans-serif; text-align: justify; background: rgb(217, 217, 217);\" data-pasted=\"true\"><span style=\"box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; color: black; font-size: 11px; font-family: verdana, sans-serif;\">QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. &nbsp;In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. 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