Lavori attuali relativi a Clinical Research Associate - Milan - Medpace, Inc.


  • Milan, Italia AL Solutions A tempo pieno

    AL Solutions is currently searching for a motivated and experienced Clinical Research Associate (CRA) to join their top 5 CRO clients team in Milan, Italy. As a CRA, you will play a crucial role in the execution and management of clinical trials, ensuring adherence to protocols, regulations, and timelines.Key Responsibilities: Conduct site qualification,...


  • Milan, Italia PSI A tempo pieno

    Job Description As a  Clinical Research Associate  at PSI Italy you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. Hybrid working arrangement in Milan area or homebased in other regions of Italy Responsibilities: Conduct and...


  • Milan, Italia AB Lavoro A tempo pieno

    Descrizione aziendaSiamo una società di consulenza, specializzata nella ricerca e selezione del personale, autorizzata dal Ministero ad operare come Agenzia per il Lavoro (Aut. Min. Lav. n. 13/I/5640), su tutto il territorio nazionale.Che tu voglia inserirti nel mondo del lavoro, o sia alla ricerca di nuovi stimoli professionali, AB Lavoro è pronta a...


  • Milan, Italia Worldwide Clinical Trials A tempo pieno

    Requisition Number7552Employment Type:Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...


  • Milan, Italia AstraZeneca A tempo pieno

    At AstraZeneca we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As a Clinical Research Associate (CRA) in Italy, you will play a pivotal role in channelling our scientific...


  • Milan, Italia IQVIA A tempo pieno

    Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions • Complete appropriate therapeutic, protocol and clinical...


  • Milan, Italia Allucent A tempo pieno

    At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Clinical Research Associate II (CRAII) to join our A-team (hybrid*/remote). As a CRAII at Allucent, you will independently...


  • Milan, Italia Allucent A tempo pieno

    At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you will independently...


  • Milan, Italia Allucent A tempo pieno

    At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you will...


  • Milan, Italia Allucent A tempo pieno

    At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Clinical Research Associate II (CRAII) to join our A-team (hybrid*/remote). As a CRAII at Allucent, you will independently...


  • Milan, Italia IQVIA A tempo pieno

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...


  • Milan, Italia PSI A tempo pieno

    Job Description Take your career to the next level and lead challenging full-service global clinical research projects, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study. Your responsibilities will include: Management of global, multi-center clinical research projects in a variety of...


  • Milan, Italia IQVIA A tempo pieno

    Clinical Trial Management and Central Trial Oversight services provide for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure regional/global clinical operations deliverables progress according to agreed upon timelines and...


  • Milan, Italia GE Healthcare A tempo pieno

    Job Description Summary The Clinical Application Manager will play a pivotal role in driving PDx Italy strategy leading the Application Team to gain efficiency and effectiveness on products positioning, standardization, priorities setting and plan execution. The individual plays an important role in defining and executing the PDx product portfolio...


  • Milan, Italia Parexel A tempo pieno

    When our values align, there's no limit to what we can achieve.   The Senior Clinical Operations Leader is responsible for coordinating the functional team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Clinical Operations deliverables (timeline, quality, productivity) are met....


  • Milan, Italia IQVIA A tempo pieno

    Job Overview Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in...


  • Milan, Italia Boston Scientific A tempo pieno

    Location: the position is open on a remote working schedule, based within the main big cities all around Italy, to ensure best travel connections. About the Role: Join our dynamic Italian Vascular Peripheral Interventions team as a Field Clinical Specialist (FCS). In this role, you will provide crucial clinical, technical, and educational support to...

  • Market Access Specialist

    1 settimana fa


    Milan, Italia Abbott A tempo pieno

    About Abbott in Italy: Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. In Italy, Abbott has a strong presence,...


  • Milan, Italia Boston Scientific A tempo pieno

    Additional Locations:  N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest...


  • Milan, Italia Boston Scientific A tempo pieno

    Additional Locations:  Italy-Bergamo Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With...

Clinical Research Associate

4 mesi fa


Milan, Italia Medpace, Inc. A tempo pieno
Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to have an

exciting career

in the research of drug and medical device development while

making a difference

in the lives of those around them. For those with a

medical and/or health/life science background

who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market -

this could be the right opportunity for you

Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include:

Nursing

Dietetics

Pharmacist

Pharmaceutical/Device Sales Representative

Biomedical/Chemical Engineer

PhD/Post-Doc

Pharm.D candidates

Health and Wellness Coordinators

Clinical Research Coordinators

Research Assistants

MEDPACE CRA TRAINING PROGRAM ( PACE )

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.

Through our

PACE

Training Program, you will join other

P rofessionals

A chieving

C RA

E xcellence:

PACE

provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.

PACE

will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.

To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

WHY BECOME A CRA

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices.

The CRA position provides many other distinctive advantages including:

Dynamic working environment, with varying responsibilities day-to-day

Expansive experience in multiple therapeutic areas

Work within a team of therapeutic and regulatory experts

Defined CRA promotion and growth ladder with potential for mentoring and management advancements

Competitive pay.

Bonus for CRA with 1,5 - 5 years of monitoring experience.

Responsibilities

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;

Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;

Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating

protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;

Verification that the investigator is enrolling only eligible subjects;

Regulatory document review;

Medical device and/or investigational product/drug accountability and inventory;

Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;

Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and

Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

Master degree in health-related field;

Willing to travel 60-80% nationally;

Familiarity with Microsoft® Office;

CRA certification completed (as per DMC 15/11/2011)

Fluent in English and Italian language;

Strong communication and presentation skills a plus.

Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace? When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Organic Growth: Medpace is continuing to grow in all areas globally and has built an expansive research campus at its headquarters in Cincinnati, OH. In 2020, Medpace opened a new seven story building that is approximately 250,000 SQFT. In total, the headquarter's campus includes five buildings and approximately 600,000 SQFT. The company also has expanding office locations in Dallas, TX and Denver, CO.

Perks ( vary by location and position ):

On-site fitness center(s)

Campus walking paths

Company-sponsored social and wellness events

Official Sponsor of FC Cincinnati

Hybrid work-from-home options and flexible work schedule

On-site Market Place

Free and covered parking

Discounts for local businesses

On campus restaurants and banks coming soon

Awards:

Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer

Recognized by Forbes as one of America's Best Mid-size Companies in 2021

Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability

Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets

#J-18808-Ljbffr