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Principal Investigator
Job in
Overland Park, Johnson County, Kansas, 66213, USA
Listed on 2026-10-08
Listing for:
Altasciences
Full Time
position Listed on 2026-10-08
Job specializations:
-
Science
Clinical Research, Medical Science
Job Description & How to Apply Below
Chez Altasciences, nous travaillons tous à l'unisson pour contribuer à la découverte, au développement et à la fabrication de nouvelles thérapies médicamenteuses afin qu'elles parviennent plus rapidement aux personnes qui en ont besoin. Quel que soit votre rôle, nous jouons tous un rôle important et vous aurez un impact significatif sur la santé et le bien-être des personnes dans le monde entier.
En respectant nos valeurs de développement du personnel, d'orientation client, de qualité et d'excellence, de respect et d'intégrité, nous cherchons à favoriser un environnement de travail passionné et collaboratif et nous sommes à la recherche de personnes talentueuses et enthousiastes, comme vous, pour rejoindre notre équipe en pleine croissance ! Que vous soyez un récent diplômé de l'université ou à la recherche de votre prochaine opportunité de carrière, il est temps de découvrir votre avenir chez Altasciences.
Nous sommes meilleurs ensemble et c'est ensemble que nous sommes Altasciences.
About
The Role The Principal Investigator is responsible for the supervision and delegation of the tasks related to the clinical trial they are Principal Investigator of. The Principal Investigator will promote Good Clinical Practices (GCP) during the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to regulation/guidance and standard operating procedure (SOP).You'll
Do Here Supervise the clinical activities for the clinical trial they are Principal Investigator.
Delegation of trial related tasks and the review of employees on the Delegation of Authority and Signature Log per job title/training record.
Perform protocol training.
Provide documentation for the Sub-Investigators.
Ensure subject safety at all times, this may include but is not limited to: review of clinical laboratory results and/or other test results. Review and/or performance of vital signs, ECGs or other safety tests.
Perform critical trial related tasks and/or make trial related decisions during the course of the trial.
Ensure subject eligibility is met based on protocol inclusionary/exclusionary criteria and that the subject continues to meet eligibility criteria throughout the course of a clinical trial.
Ensure requirements related to obtaining informed consent are met.
Perform physical examinations and medical history intake and on-site for surveillance as required by protocol and remain available on-call for medical events.
Record and follow-up on adverse events and determine causality.
Report serious adverse events to appropriate parties.
Participate in sponsor visits and regulatory audits.
Document study related events incompliance with GCP.Review study protocols and SOPs.Complete and/or review regulatory documents as applicable.
Participate in sponsor visits and regulatory audits.
May act as Sub-Investigator on studies not assigned to them as Principal Investigator.
What You'll Need to SucceedMD degree from an accredited Physician Program and Advanced Cardiac Life Support (ACLS) certification required.
Previous experience with similar responsibilities; ideally related to the industry.
What We Offer Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences’ Benefits Package Includes:
Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match Paid Vacation and Holidays Paid Sick and Bereavement Leave Employee Assistance & Telehealth Programs Altasciences’ Incentive Programs Include:
Training & Development Programs Employee Referral…
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