Italy: Late-Phase Clinical Research Associate
Resourcing Life Science
A Global CRO is seeking an experienced Clinical Research Associate Late Phase in Italy. The role involves monitoring clinical studies in phases II-III, ensuring adherence to Good Clinical Practices, and conducting site initiation and closure. Candidates should possess a Bachelor degree in life science, at least 1 year of relevant CRA experience, and be fluent in both English and Italian. Excellent communication skills are essential. This position is crucial for ensuring compliance and successful study conduct. #J-18808-Ljbffr
- ...They offer a full service solution encompassing clinical & non‑clinical development, peri‑approval &... ...They are currently seeking a CRA / Clinical Research Associate in Italy. Job Overview Monitoring clinical studies in phases II-III Assuring adherence to Good Clinical Practices...Suggested
- ...A leading clinical research organization is seeking full-time Clinical Research Associates in the Town of Italy, New York. This role will involve monitoring research sites, ensuring compliance, and assisting in the clinical trials process. Candidates should possess a Master...SuggestedFull timeFlexible hours
- ...Our Client is a rapidly growing international Clinical Research Organisation offering an experienced( Senior ) CRA opportunity to work from home on full FTE as part of their team in Italy . Responsibilities: Conducting start-up activities and monitoring visits Maintaining...SuggestedWork from home
- ...Our clinical activities are growing rapidly, and we are currently seeking... ...home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a... ...organization (CRO). We provide Phase I-IV clinical development...SuggestedFull timeContract workWork at officeLocal areaImmediate startWork from homeFlexible hours
- ...Overview Job Summary: Coordinate various research trials for the Institute for Global Health, including early or late phase FDA-regulated trials, and ensure compliance with... .... Enroll, register and screen patients for clinical research trials; collect and submit clinical...SuggestedFull timeWork at officeMonday to Friday
- ...passionate about oncology research and looking to join a... ...(TRIO) is a global clinical research organization dedicated... ...a Clinical Research Associate to join our Monitoring... ...will be home-based in Italy. Responsibilities: Conducting... ...in monitoring early-phase trials Fluent in...Local areaWork from homeFlexible hours
- ...Overview Experienced Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated biopharmaceutical solutions organization... ...completes assigned training as required. For Real World Late Phase, the CRA II will use the business card title of Site...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$24 - $26.92 per hour
...Description Job Description Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network... ...growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety...Hourly payWork at officeFlexible hours$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated Location: Gloucester, United States of America | Full time | Field-based | R1541733 To be eligible... ...data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available...Full timePart timeLocal areaImmediate start- ...and impact when it matters most and support from direct line management. Precision for Medicine is open to Clinical Research Associates I to join our team in Italy. This is a remote based position (homebased anywhere in Italy), with travel to sites for monitoring visits...Remote workNight shift
- ...Clinical Study Coordinator Primary responsibilities of the position Serves as a primary contact between the company and study... ...coordination with study groups (CSL/CTA/DM) throughout the study phase. Reports back to CSL for IMVs status/follow-up actions in a...Work experience placementWork at officeLocal area
$60.41k - $65k
...Job Summary: The Clinical Research Associate I (CRA I) will join a team of experienced associates and manage various research trials, including first in human through phase 3 trials. The role will be expected to manage 2-3 studies simultaneously. The will ensure compliance...Full timeWork at officeMonday to FridayFlexible hoursAfternoon shift$125k - $145k
...SOPs and regulatory requirements, i.e. Good Clinical Practice (GCP) and International... ...index and medidata as necessary. Supports research sites with local Institutional Review Board... ...environment of remote collaborators. EU (Italy): Certified Monitor in compliance with Italian...Contract workLocal areaRemote workFlexible hours- ...Veeda Lifesciences is seeking a Clinical Research Associate (CRA) based in Italy for its growing international hematology/oncology Clinical Trials program. The position is offered on a freelance basis. Job overview: The CRA is responsible for ensuring that the conduct...Work experience placementFreelanceLocal areaFlexible hoursNight shiftAfternoon shift
$24 - $26.92 per hour
Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development... ...growing research site network specializing focused on late phase industry‑sponsored trials of novel treatments for a variety...Hourly payWork at officeFlexible hours- ...Senior Clinical Research Associate (US) Remote Position Summary The Sr. CRA is responsible for the oversight and monitoring clinical trials to ensure... ...facts and data to guide decisions. Experience working on phase 2 and 3 registrational trials is preferred Working...Interim roleRemote work
$65k - $80k
...Job Summary The Clinical Research Associate II (CRA II) will join a team of experienced coordinators and manage various research trials, including first in human through phase 3 trials. The role will be expected to manage 4 or more studies simultaneously. The CRA II will...Work at officeMonday to FridayFlexible hoursAfternoon shift- ...Senior Clinical Research Associate job at PSI CRO. Remote. We are the company that cares – for our staff, for our clients, for our partners and for... ...minimum) Experience in all types of monitoring visits in Phase I-III Participation in clinical projects as a Senior Monitor...Remote workWork from homeWork visa
- ...Mount Sinai Morningside is seeking a Clinical Research Associate I to oversee the clinical research trial lifecycle, from site management to closure... ...1-2 years of experience in clinical research, particularly Phase I-IV studies. Join us to contribute to our commitment to...
- ...Medpace, Inc. is seeking full-time Clinical Research Associates to join their Clinical Monitoring team, based in Italy. The role involves conducting monitoring visits, verifying compliance with study protocols, and assessing the recruitment success at clinical research...Full timeFlexible hours
$58.66k - $81.68k
...Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) lifecycle responsibilities including site management, ongoing maintenance and closure of pre-clinical, Phase I through Phase IV, and post-marketing studies. Responsibilities...TraineeshipLocal area- ...involves collaboration with cross-functional clinical study teams and investigator site... ...of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance... ...experience in a CRO or pharma organization Phase I Oncology monitoring experience...Interim roleWork at officeLocal areaRemote work
$71.9k - $189k
...IQVIA is looking for a Clinical Research Associate based in New York to perform site monitoring visits and manage the progress of assigned studies. Candidates should have a minimum of 2 years of on-site monitoring experience and a Bachelor's Degree in a scientific discipline...- ...language model-based system built to understand and assess clinical characteristics in EMRs. Synapsis AI is designed for installation... .... As a vital member of our diverse team, our Clinical Research Associates (CRA) will collaborate closely with the AI Research and software...Local areaFlexible hoursShift work
$57.5k - $226.8k
...Bachelor's Degree in a scientific discipline, along with a minimum of 2 years of on-site monitoring experience. Strong knowledge of Good Clinical Practice and excellent communication skills are essential. Compensation ranges from $57,500 to $226,800, based on qualifications...$91.34k - $114.17k
...Clinical Research Associate - Oncology - New York City ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission...Work experience placementLocal areaVisa sponsorshipFlexible hours- ...Clinical Research Associate - Cross Therapeutic Area - Miami ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission...Local areaVisa sponsorshipFlexible hours
$91.5k - $137.3k
...involving start-up and study implementation, on-site monitoring of clinical research studies as well as on-going site management. Incumbents work... ...according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies...Contract workLocal areaRemote workNight shift- ...Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate documentation for clinical research. As a CRA, you monitor clinical tasks for correct functioning and completion,...RelocationVisa sponsorship
- ...As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures...Contract workWork from home
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