Precision Medicine Group
Clinical Research Associate I/ Clinical Research Associate II
Precision Medicine Group, Sauk Trail Beach, Wisconsin, United States
Clinical Research Associate I / II
Precision for Medicine is a unique clinical research organization that combines new technologies, expertise, and operational scale to improve the speed, cost, and success of bringing life‑changing therapies to patients. We focus on oncology and rare disease and pride ourselves on high CRA retention rates, a lower‑than‑average number of protocols per CRA (allowing each CRA to become a protocol expert), and a culture where your voice is heard.
About You
You are calm, thoughtful, and responsive when things don’t go as planned.
You are well‑prepared for investigator meetings, site visits, or project team updates, always staying two steps ahead.
You find quick and creative ways of overcoming difficulties.
You have an impeccable eye for detail.
You identify potential study risks and propose mitigation solutions.
You take responsibility for the quality and outcomes of your work.
You are adept at handling conflict using tried‑and‑true resolution strategies.
Responsibilities
Monitor and own the progress of clinical studies at investigative sites.
Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH‑GCP, and all applicable regulations and standards.
Coordinate activities required to set up and monitor a study (e.g., identify investigators; prepare regulatory submissions; conduct pre‑study and initiation visits).
Qualifications Minimum Required:
Life‑science degree or equivalent experience.
At least 1 year as a CRA in a CRO or pharmaceutical/biotech environment, with site management or equivalent experience.
Experience managing oncology studies.
Availability for domestic travel, including overnight stays, and readiness for up to 50‑60% travel commitment.
Other Required:
Excellent communication and organizational skills; team player.
Evidence of a client‑focused approach.
Fluency in English, Dutch, and French.
Preferred:
Experience with study start‑up activities.
Please apply in English. Any data provided as part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, colour, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
We want to emphasize that any job offers presented by individuals or organizations claiming to be an employer are not associated with our company and may be fraudulent. Our organization will not extend a job offer without prior communication with our recruiting team, hiring managers, and a formal interview process.
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About You
You are calm, thoughtful, and responsive when things don’t go as planned.
You are well‑prepared for investigator meetings, site visits, or project team updates, always staying two steps ahead.
You find quick and creative ways of overcoming difficulties.
You have an impeccable eye for detail.
You identify potential study risks and propose mitigation solutions.
You take responsibility for the quality and outcomes of your work.
You are adept at handling conflict using tried‑and‑true resolution strategies.
Responsibilities
Monitor and own the progress of clinical studies at investigative sites.
Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH‑GCP, and all applicable regulations and standards.
Coordinate activities required to set up and monitor a study (e.g., identify investigators; prepare regulatory submissions; conduct pre‑study and initiation visits).
Qualifications Minimum Required:
Life‑science degree or equivalent experience.
At least 1 year as a CRA in a CRO or pharmaceutical/biotech environment, with site management or equivalent experience.
Experience managing oncology studies.
Availability for domestic travel, including overnight stays, and readiness for up to 50‑60% travel commitment.
Other Required:
Excellent communication and organizational skills; team player.
Evidence of a client‑focused approach.
Fluency in English, Dutch, and French.
Preferred:
Experience with study start‑up activities.
Please apply in English. Any data provided as part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, colour, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
We want to emphasize that any job offers presented by individuals or organizations claiming to be an employer are not associated with our company and may be fraudulent. Our organization will not extend a job offer without prior communication with our recruiting team, hiring managers, and a formal interview process.
#J-18808-Ljbffr