Clinical Research Associate​/Senior CRA; Italy

Position: Clinical Research Associate / Senior CRA (Italy) Location: Town of Italy Overview reputed company is not your typical CRO. At reputed company we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success reputed company 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 reputed company 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 reputed company it matters most and support from direct line management. We are looking for an reputed company CRA or Senior CRA to join reputed company in Italy. You will have previous monitoring experience for Oncology clinical Studies in Italy. This is a remote based position ( homebased reputed company in Italy ), with travel to sites for monitoring visits. About you

• You are reputed company, thoughtful, and reputed company reputed company things don’t go as planned.
• You are well-reputed company, whether it be for an investigator meeting, site visit or project team update, always staying two steps reputed company 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 reputed company you busy and support your growth You will monitor and own the reputed company of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and reputed company applicable regulations and standards. You will coordinate reputed company 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

• Life science degree and / or equivalent experience
• CRA experience reputed company the CRO or pharmaceutical industry (and working in Oncology). We require a minimum of 1 year experience as a CRA in Oncology, and can offer CRA II and Senior CRA titles depending on experience level.
• Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)

Preferred

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Two+ years of oncology experience
• Study start up activities experience would be an advantage
• For Senior CRAs, understanding of financial management and mentoring experience would be desirable

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