CRA II

Piedmont, Italy

Job description

We see human behind every number

Clinical Research Associate II

Location: Italy (home-based)

On behalf of our partner, one of the global leaders in clinical research, we are currently recruiting for a Clinical Research Associate II in Italy to work for a global biotechnology company.

As a CRA II in Italy you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be partnering with one of the worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

Detailed Job Duties and Responsibilities

  • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation

  • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions

  • Balancing sponsor generated queries

  • Taking responsibility for study cost efficiency

  • Preparation and review of study documentation and feasibility studies for new proposals

  • Potential to assist in training and mentoring fellow CRAs

Education / Qualifications / Skills Requirements

  • 18 months+ of independent monitoring experience in phase I-III trials as a Certified CRA

  • College degree in medicine, science, or equivalent

  • Previous independent monitoring experience in medium-sized studies, including study start-up and close-out

  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data

  • Excellent written and verbal communication in English

  • Ability to work to tight deadlines

  • Availability to travel least 60% of the time (international and domestic -fly and drive)

  • Experience in Oncology is mandatory

Benefits:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead

  • Global Employee Assistance Program

  • Life assurance

  • Country-specific flexible benefits, including options like gym membership discounts, childcare vouchers, and more.

KCR is a clinical development solutions provider creating value for emerging biotechnology organizations.  

Founded in 1997, our expert teams support clients with full-service clinical development capabilities. As part of the ICON organization, KCR serves clients globally with key operations hubs in Boston, US, Berlin, Germany, and Warsaw, Poland. KCR’s bespoke approach to service delivery for emerging Biotech companies combined with the global reach and scale of the ICON organization brings a uniquely comprehensive solution to the CRO market.  For more information visit www.kcrcro.com.   

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Providing your personal data is voluntary, however, if you do not provide us with the necessary information, we will not be legally allowed to get in touch with you and consider your application. By sending application documents containing your personal data to a wider extent than required by provisions of the applicable laws, you are granting consent for the data to be processed for the purposes of the ongoing recruitment.

If you would like your candidacy also to be considered for future recruitments, please select an additional consent or add the following statement to your application documents: “I agree to the processing of my personal data for any future recruitments conducted by KCR and/or KCR affiliates for a period of up to 3 years”. Such consent may be placed in your CV or electronic correspondence addressed to your potential employer.

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You can contact KCR Group Data Protection Officer at gdpr@kcrcro.com any time with any questions or concerns regarding how your personal data is processed.

KCR is an equal opportunity employer. In line with our motto, ‘We see human behind every number,’ KCR is committed to fostering an inclusive culture and maintaining a diverse, safe, and respectful working environment with equitable treatment for all.

We are committed to non-discriminatory practices and provide an equal opportunity for all qualified employees and job applicants within all employment sectors. We believe that in developing a desirable culture of belonging in which diverse perspectives and voices are welcomed and heard, the full potential of employees can be achieved.

If you require reasonable accommodations to participate in the application process, please let us know by email: eeo@kcrcro.com. We are committed to ensuring equal opportunity for all applicants and will work to provide reasonable accommodations to support your needs.


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