Precision Medicine Group
Precision Medicine
PrincipalClinicalScientist
Neural analysis suggests this role is
optimal for Principal candidates.
“Principal Clinical Scientist at Precision Medicine Group. Skills: Clinical Science Analytics, oncology, medical terminology, clinical trial data, disease assessment criteria, standards of care, grading criteria, FDA & ICH-GCP, clinical trial process, data visualization software, JReview. Clinical Science Analytics. application of disease assessment criteria, standards of care, grading criteria, etc.”
What You'll Achieve.
Results oriented
Industry & Context.
critical thinking; decision making; analytical &conflict management skills; ability to strategically plan & apply effective risk management
Ability to occasionally travel domestically & internationally including overnight stays
What They're Looking For.
Must Have
Clinical trial data, FDA & ICH-GCP, clinical trial process, clinical research functional departments
Nice to Have
Medical related degree, RN, OCN, RPH, PharmD, Database build experience, On-site monitoring experience &/or data review experience, data visualization software such as JReview, solid & liquid tumors, phase I, II & III studies, global trials
What You'll Do.
Clinical Science Analytics
application of disease assessment criteria
manage the CSAI operational function in a global
cross-functional environment
How You'll Work.
Team & Collaboration
global, cross-functional environment
Communication Scope
Ability to occasionally travel domestically & internationally including overnight stays; Excellent presentation; verbal; written communications skills
Process & Methodology
strategically plan & apply effective risk management, functional area project level
Full Job Description
Position Summary: The Principal Clinical Scientist, Clinical Science Analytics both written & oral Ability to occasionally travel domestically & internationally including overnight stays Preferred: Medical related degree, RN, OCN, RPH, PharmD, etc. Database build experience On-site monitoring experience &/or data review experience Experience with data visualization software such as JReview Experience in solid & liquid tumors Experience in phase I, II & III studies Experience in global trials Skills & Competencies: Demonstrates highly advanced knowledge in oncology & medical terminology with ability to apply knowledge to clinical trial data including the application of disease assessment criteria, standards of care, grading criteria, etc. Desire to continually learn & keep up to date on medical & oncology standards of care with the ability to self-research & educate. Working knowledge of FDA & ICH-GCP, relevant SOPs & regulatory guidance with a well-rounded knowledge of the entire clinical trial process & working understanding of clinical research functional departments High level of integrity from a professional & ethical perspective Ability to independently manage the CSAI operational function in a global, cross-functional environment with awareness of appropriate escalation. Excellent time management, negotiation, critical thinking, decision making, analytical &conflict management skills with the ability to strategically plan & apply effective risk management. Exhibits self-motivation with the ability to work remotely while independently lead, support & inspire excellence. Demonstrates ability to adjust to multiple demands & shifting priorities. Results oriented, accountable, motivated, cooperative, & flexible Ability to apply financial management skills at the functional area project level. Excellent presentation, verbal, & written communications skills Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA ap
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