Attiva gli avvisi di lavoro via e-mail!
Aumenta le tue possibilità di ottenere un colloquio
Crea un curriculum personalizzato per un lavoro specifico per avere più probabilità di riuscita.
An innovative company is seeking an experienced Clinical Research Associate or Senior CRA to join their remote team in Italy. This role offers the chance to work on impactful oncology studies while enjoying a supportive work environment that values your input. With a focus on work-life balance and reasonable travel, you'll be able to influence clinical trial execution and mentor junior staff. This position is perfect for those looking to grow their career in a collaborative setting that prioritizes quality and results.
Social network you want to login/join with:
col-narrow-left
Other
-
Yes
col-narrow-right
dd23877e8309
1
06.05.2025
20.06.2025
col-wide
Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.
We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result.
Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
We are looking for an experienced CRA or Senior CRA to join our team in Italy. You will have previous monitoring experience for Oncology clinical Studies in Italy.
This is a remote based position (homebased anywhere in Italy), with travel to sites for monitoring visits.
About you:
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.
Requirements:
Preferred: