In Job is an International Talent Search Company based in Verona and present in Europe, Russia, United States and Asia.
We provide professional staffing services and skilled recruitment for permanent and temporary positions with a proven track record of filling high potentials, experts, specialists and middle executives within leading private organizations.
Internally we have an impressive range of multi-sector-experienced industry leaders and traditional recruiters. Over the years we've placed more than 110.000 people in different fields. Thanks to our long experience we are able to offer the knowledge, the contacts and the conditions required to achieve a professional growth to those who rely on us.
For our client an innovative international pharmaceutical company that continually provides new drugs to patients around the world, we are looking for:
The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects. He/She will need to perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out" of the trial. The Clinical Research Associate will be also responsible for determining protocol and regulatory compliance on the sites; and for thriving in multi-national project teams
in order to deliver exemplary levels of customer service
The opportunity is suitable for a professional with proven experience within a CRO, pharmaceutical or biotech company on a similar position. We're specifically looking for a qualified professional with 2-3 years of experience in interventional studies focused on. Experience within Oncology, Haematology, Pulmonary diseases would be as well considered a strong advantage.
You will need to possess a relevant degree in in pharmacy, life science or related field; proven clinical trial monitoring skills and the ability to conduct monitoring activities independently. Additional requirements also include:
- Excellent standard of verbal and written communication skills in English language;
- In-depth understanding of ICH/GCP guidelines;
- Highly organized with strong attention to detail and deadlines;
- Advanced skills across all of the MS Office packages;
- Willingness to travel.