Precision Medicine Group

Precision Medicine

PrincipalClinicalScientist

Mexico, Mexico Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Principal candidates.

The Brief

“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.

Precision Medicine
Problems you'll solve

critical thinking; decision making; analytical &conflict management skills; ability to strategically plan & apply effective risk management

Eligibility Requirements

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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