Clinical Trials Leader

יקנעם עילית |
1-2 שנים |
משרה מלאה
| לפני 13 שעות
תיאור משרה

About Medtronic
Bold thinking. Bolder actions. We are Medtronic.
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world.
In everything we do, we are engineering the extraordinary.
A Day in the Life
In this position, you will be managing clinical R&D trials as part of our Clinical Affairs team.
You will design and write protocols and amendments for assigned clinical studies
· You will prepare ICF, investigator brochures, patient information sheet, CRF, study plans, etc.
· You will prepare applications for ethics committee/worldwide IRB submissions
· You will organize investigator meetings
· You will train clinical study staff on all study procedures
· You will execute clinical studies from initiation to COV till the final report is obtained (including publications)
· You will review interim/final reports
· You will be attending international conferences to improve scientific knowledge and network.
r Careers that Change Lives
We’re a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Join our team in Clinical Affairs and help shape policies that change lives.
Work with us to incentivize better patient care, and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.

Come strengthen your specialized skills and enhance your expertise. We’ll support you with the training, mentorship, guidance, and networks you need to advance and empower you to work in the way that’s best for you.

דרישות התפקיד

Must Haves
· B.A/Bsc in relevant life science/ medical affairs/ engineering field
· 1-3 years of experience managing clinical trials (from planning and protocol design to execution)
· previous experiences as a CRA/ Monitoring /CRS
· Ability to travel 10-20%
Nice to Haves
· Relevant MSc/ PhD

* משרה זו פונה לנשים וגברים כאחד.