About You
You are calm, thoughtful, and responsive when things don’t go as planned.
You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
You find quick and creative ways of overcoming difficulties.
You have an impeccable eye for detail.
You identify potential study risks and propose solutions on how to mitigate them.
You take responsibility in the quality and outcomes of your work.
You are adept at handling conflict by using tried and true resolution strategies.
How We Will Keep You Busy and Support Your Growth
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH‑GCP, and all applicable regulations and standards.
You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre‑study and initiation visits, etc.).
Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.
You will also have the opportunity to train and mentor junior staff members.
You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Qualifications
Minimum Required:

4-year college degree or equivalent experience
Holder of CRA certificate

Other Required

CRA experience within the CRO or pharmaceutical industry; 2+ years for a CRA II and 3+ years for Senior CRAs
Oncology experience
Availability for domestic travel including overnight stays, which may constitute up to approximately 50‑60% travel commitment (international travel may be required for some senior level positions)
Fluency in English and for non‑English speaking countries the local language of country where position based

Preferred

Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
Two+ years of oncology experience
Study start up activities experience
For Senior CRAs, understanding of financial management

Please, apply in English.
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, 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.
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