Crea un profilo in modo da poter essere trovato dalle aziende, ottenere offerte di lavoro più adatte alle tue esigenze e candidarti più velocemente.
  • Cerca lavoro
  • Preferiti
  • Crea CV
    Novità
  • Stipendi
  • Iscrizioni

CRA II

Icon Clinical PLC

Overview

In this role, you contribute to the design, analysis, and oversight of clinical trials to support faster access to innovative therapies. You will perform monitoring activities, ensure patient safety, data integrity, and protocol compliance within a collaborative team. You'll work with investigators and site staff to keep studies on track and deliver high-quality study documentation. This position offers the chance to impact patient care at a global, value-driven organization with opportunities for professional growth.

Retribuzione / Benefits

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Responsabilità

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborate with investigators and site staff to facilitate smooth study conduct
  • Perform data review and resolution of queries to maintain high-quality clinical data
  • Contribute to preparation and review of study documentation, including protocols and clinical study reports

Requisiti fondamentali

  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Willingness to travel approximately 60%
  • Strong communication skills
  • Attention to detail
  • Ability to work both independently and in a team
  • Collaborative mindset in fast-paced environments
  • ICH-GCP guidelines
  • Clinical trial processes knowledge
Offerta di lavoro pubblicata 1 giorno fa
Offerte di lavoro simili
  •  ...fondamentali Bachelor's and Master's Degree in scientific discipline or health care At least 3 years of on-site monitoring experience CRA Certification according to Ministerial Decree dated 15.11.2011 Knowledge of GCP and ICH guidelines Therapeutic and protocol... 
    Consigliato

    IQVIA

    Pavia (PV)
    1 giorno fa
  •  ...reports and follow-up letters with findings and corrective actions Requisiti fondamentali Master degree in health-related field CRA certification completed per DMC 15/11/2011 Previous experience as CRA Willingness to travel up to 60-80% nationally... 
    Consigliato
    Orario flessibile

    Medpace

    Pavia (PV)
    1 giorno fa
  • Overview In this Medical Affairs role, you support intraocular lens proctoring and medical information requests to ensure optimal patient outcomes. You analyze IOL case data, coordinate MIR responses, and generate performance insights in alignment with J&J Vision policies...
    Consigliato
    Orario flessibile

    Johnson & Johnson

    Pavia (PV)
    1 giorno fa
  • Overview In this role you will lead imaging, training and operational support for transcatheter valve therapies in a cross-functional team. You'll educate physicians and hospital staff on imaging and procedural aspects of investigational products, while providing real...
    Consigliato
    Remoto
    Orario flessibile

    Edwards Lifesciences

    Pavia (PV)
    1 giorno fa
  • Overview In this role you drive the global Real World Evidence (RWE) strategy for the Endo-Met portfolio, aligning evidence plans with research and commercial goals. You lead cross-functional execution, shaping partnerships and data sourcing to inform regulatory, payer...
    Consigliato
    Remoto

    Chiesi

    Pavia (PV)
    1 giorno fa
  • Overview Join Reply in a role focused on Public Sector & Healthcare. You will engage in innovative technology projects within a consulting and digital services context, collaborating with cross-functional teams. You will tackle diverse challenges at the intersection...
    Stage/Tirocinio

    Reply

    Pavia (PV)
    1 giorno fa
  • Overview As Project Manager at Alira Health, you will drive the efficient execution of study protocols within scope, budget, and regulatory guidelines. You will partner with the Clinical team, sponsors, and vendors to keep trials on track and deliver timely status updates...

    Alira Health

    Pavia (PV)
    1 giorno fa