Italy Lead CRA - Phase II-III Monitoring
Resourcing Life Science
A global CRO is seeking a Clinical Research Associate to monitor clinical studies in phases II-III. Responsibilities include ensuring compliance with Good Clinical Practices, supervising study conduct, and initiating investigator sites. The ideal candidate holds a bachelor's degree in life-science, has at least 1 year of monitoring experience within a CRO, and is fluent in English and Italian. This position offers a full-time employment opportunity in Italy. #J-18808-Ljbffr
- ...clinical development, peri-approval & market access. They are currently seeking a CRA in Netherlands. The role is sponsor dedicated via the CRO Job Overview Monitoring clinical studies in phases II-III Assuring adherence to Good Clinical Practices, investigator integrity, and...Suggested
- ...A global Clinical Research Organization is seeking a Clinical Research Associate in New York to monitor clinical studies and ensure adherence to Good Clinical Practices. The ideal candidate has a Bachelor's degree in life-science and at least one year of monitoring experience...Suggested
- ...development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate Regional Monitoring in Italy Job Overview Monitoring clinical studies in phases II-III Assuring adherence to Good Clinical Practices, investigator integrity, and...Suggested
- ...Clinical Research Associate to oversee clinical trial activities in Italy. The role involves ensuring compliance with study protocols and... ...should have an advanced degree in life sciences, significant CRA experience, and excellent communication skills. Benefits include...SuggestedRemote workFlexible hours
$115k - $140k
...Fortrea is looking for a Senior Clinical Research Associate (CRA 2) based in New York. This role requires 4+ years of Clinical Monitoring experience with a strong emphasis on Oncology monitoring. You will be responsible for monitoring clinical trial sites, ensuring compliance...Suggested- ...RBW Consulting is seeking a Senior Clinical Research Associate (CRA II) to oversee clinical trial activities across Italy. This role involves monitoring compliance with protocols, collaborating with teams for data accuracy, and building strong relationships with site...Flexible hours
- ...Syneos Health is looking for a Single Sponsor CRA I / II to perform site qualification and monitoring activities in the United States. Ideal candidates will have a Bachelor’s degree or RN in a related field, along with knowledge of Good Clinical Practice and ICH Guidelines...
$70.1k - $126.1k
...Syneos Health / inVentiv Health Commercial LLC is looking for a CRA II - Sponsor Dedicated. This remote position requires managing... ...regulations and protocol. Responsibilities include site qualification, monitoring, and communicating with study site personnel. Candidates should...Remote workFlexible hours$90k - $140k
...A leading clinical research organization is seeking a Clinical Research Associate II or Senior CRA with a focus on Psychiatry or Pain. This remote role involves extensive site monitoring, ensuring adherence to regulations, and engaging in project management activities...Remote work$91.5k - $137.3k
...clinical research organization is seeking a Clinical Research Associate II to oversee study site management in a remote capacity. Ideal... ...a degree in a scientific discipline and at least two years of CRA experience, especially in oncology trials. The role requires excellent...Remote work$40 - $47 per hour
...Proclinical Staffing is seeking a Lead Clinical Research Coordinator in Bronx, NY to manage and facilitate clinical trial activities. This role requires 4-5 years of experience running Phase II-III trials, a Bachelor’s degree, GCP Certification, and fluency in both English...Hourly pay- ...Syneos Health is seeking a Senior Clinical Research Associate (CRA) with strong oncology experience located in Town of Belgium, Wisconsin... ...the pharmaceutical industry, managing site qualification and monitoring. Responsibilities include ensuring compliance with regulatory...Remote work
- ...IQVIA in New York is seeking a Clinical Research Associate (CRA) to join our team dedicated to advancing clinical research and improving patient outcomes. In this role, you'll lead site monitoring, ensure compliance with GCP/ICH guidelines, and collaborate with cross-...
$105k - $117k
...Fortrea is looking for Experienced Device CRA 2s to support their Medical Device & Diagnostics team. This role involves overseeing clinical trials with a strong focus on site monitoring, patient safety, and data integrity. Ideal candidates will have a relevant university...- ...Research Associates I to join their remote team. The role involves monitoring clinical studies, ensuring compliance with regulations, and... ...will hold a degree in life sciences and have at least 6 months of CRA experience. Candidates must be fluent in English and Italian,...Remote work
- ...with manageable travel requirements. CRAs will be responsible for monitoring clinical studies and ensuring compliance with protocols and... ...possess a life science/healthcare degree and a minimum of 6 months CRA experience. Fluency in English and Italian is required. Join a...Remote work
- ...A leading CRO is seeking a Senior CRA for a permanent home-based role in Poland. The position involves conducting clinical trial monitoring, ensuring compliance with protocols and regulations, and mentoring junior staff. Candidates should have a Bachelor's in life sciences...Permanent employmentRemote workWork from home
$105k - $117k
...A clinical research organization is looking for an Experienced Ophthalmology & Gen Med CRA 2 to lead a Full Service Outsourcing team. You will be responsible for monitoring clinical trial sites, ensuring compliance with protocol, and managing site operations. This role...Remote work- ...Research Corporation is looking for a Clinical Research Associate II to oversee the execution of clinical trials at Investigative... ...project issues. Responsibilities include site management, conducting monitoring visits, and ensuring compliance with FDA regulations and ICH-GCP...
$105.5k - $140k
...transplant is not currently an option. Who You Are The Monitoring Team Lead/Senior Monitoring Team Lead will plan, implement and execute... ...identify areas for proactive improvement Provide feedback on CRA performance to Clinical Monitoring Management and support...Permanent employmentContract workWork at officeRemote work$50 - $55 per hour
...Solutions has a client that is immediately hiring for Site Monitoring Lead Position type: Full Time Contract Duration: 12 months... ...positive site relationships and ensure continuity through all phases of the trial. 12. Supports the LSM in reviews, and monitoring...Hourly payFull timeContract workTemporary workWork experience placementImmediate startRemote workWorldwideFlexible hours- ...looking for a Clinical Research Associate II (CRA II) in the United States. This role... ...performing site qualification, site initiation, monitoring activities, and ensuring regulatory... ...and offers the opportunity to work with a leading life sciences organization dedicated to...
- ...ideal candidate will have over five years of CRA experience on complex studies, preferably in the... ...device sector, particularly with Class III cardiovascular rhythm management devices. Responsibilities include monitoring site engagement and collaborating with clinical...
$100k - $118k
...Overview Fortrea's FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in... ...Expert for TMF across all research phases and collaborates cross-functionally with... ...deliverables include providing TMF expertise, monitoring and assessing the overall TMF Health (...Full timePart timeWork at officeRemote workFlexible hours$115k - $125k
...A leading clinical research organization is seeking a Clinical Research Associate (CRA) for a remote permanent position based out of CST. The CRA will conduct site monitoring visits, support subject recruitment, and manage communication with study sites. Candidates should...Permanent employmentRemote work- ...A leading healthcare company is seeking an experienced Ophthalmology Clinical Research Associate (CRA) to lead its Full Service Outsourcing team. The role involves significant travel... ..., and responsibilities include site monitoring and compliance with study protocols....
- ...regulations and ICH-GCP guidelines. Responsibilities include initiating, monitoring, and closing studies, preparing regulatory submissions, and... ...a bachelor's degree in life sciences and at least two years of CRA experience. The role offers an attractive salary and a...Remote work
$83.73k
...NYU Langone Hospitals is seeking an experienced Anesthesia Tech III responsible for stocking anesthetic supplies, maintaining equipment, and assisting in patient care. The ideal candidate should have graduated from an Anesthesia Technician program and possess 5 years of...- ...Group is seeking a Senior Clinical Research Associate. You will monitor clinical studies, coordinate activities, and mentor junior staff... ...life sciences or health-related fields and at least 3.5 years of CRA experience in the CRO or pharmaceutical industry. Oncology...Remote workWork from home
$105k - $125k
...seeking experienced Ophthalmology CRAs to lead and support our Full Service Outsourcing... ...Responsible for all aspects of study site monitoring including routine monitoring and close-... ...experience Ophthalmology experience as a CRA Open to various hub locations The important...Full timePart timeWork at officeLocal areaRemote workFlexible hours
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