Qualifications
About You:
You remain composed, thoughtful, and proactive when facing challenges.
You come prepared for every meeting, site visit, or project update, consistently staying ahead of the curve.
You devise innovative solutions to overcome obstacles efficiently.
Your attention to detail is exceptional.
You recognize potential study risks and offer practical solutions to mitigate them.
You take accountability for the quality and results of your work.
You navigate conflicts effectively using established resolution strategies.
What You Will Do:
You will oversee and drive the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and all relevant regulations. This includes coordinating essential activities for study setup and monitoring such as identifying investigators, assisting with regulatory submissions, and conducting pre-study and initiation visits.
About the job
At Precision for Medicine, we redefine the role of a Contract Research Organization (CRO). Our commitment to fostering a vibrant culture is reflected in our notably high retention rates for Clinical Research Associates (CRAs), significantly surpassing industry norms.
Our CRAs enjoy fulfilling careers here, drawn not only by the passionate team but also by the exceptional quality of life we offer. With a manageable number of protocols, you will become a subject matter expert in your field. Travel commitments are reasonable, enhancing your work-life balance. Most importantly, your insights and contributions are valued; being part of a smaller CRO allows for greater influence and support from leadership.
We are seeking a Clinical Research Associate II, fully remote based in the UK.
About Precision for Medicine
Precision for Medicine is an innovative CRO dedicated to transforming the landscape of clinical research through a culture of collaboration, excellence, and commitment to scientific advancement.