Monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
Coordinate all necessary activities to set up and monitor a study, including investigator identification, regulatory submissions, and site initiation visits.
Focus on an average of one to two studies, allowing you to become a protocol expert.

About You:

You are calm, thoughtful, and responsive when things don’t go as planned, and you stay two steps ahead.
You have an impeccable eye for detail, identify potential study risks, and propose solutions.
You are adept at handling conflict with tried and true resolution strategies.

How We Support Your Growth:

You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
You will have support from direct line management and a smaller CRO environment where your voice is heard.
Travel is reasonable, ensuring a good work/life balance.

Precision for Medicine, Oncology and Rare Disease

Precision for Medicine, Oncology and Rare Disease is a precision medicine CRO that combines novel clinical trial designs, operational and medical experts, and advanced biomarker and data analytics. They pride themselves on high CRA retention rates and a culture where employees feel appreciated and have impact.

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