Icra, Italy
Proclinical are recruiting a ICRA, Italy for a CRO.
This role is on a permanent basis and is located in Milan.
The client is focused on assisting developing organisations reach their goals.
**Responsibilities**:
- Serve as the company's main point of contact with allocated sites, as well as be responsible for quality and delivery throughout the start-up phase.
- Form relations with investigators and site personnel.
- You will submit all relevant documentation to the trial master file as per project plans/promote/company policy.
- Uphold and keep suitable clinical trial management systems up to date in a timely fashion.
- When needed, you will contribute to investigator and any other meetings and audits & regulatory inspections both internally and externally.
- When requested/required, you will perform remote visits/contacts.
- Other duties may be assigned to this role.
**Skills & Requirements**:
- At least 1 - 1. 5 years of experience in a pertinent role/work environment.
- A background ideally in global CROs.
- Located close to or in Milan so as to be able to come into the office when required rendering to the FWA program.
- Fluency in the English language.
- Computer literacy in Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
- Adept to covering some Study Start Up tasks (SSU).
- Capable of resolving issues.
- Ability to assume the initiative and work self-sufficiently as well as proactively look for guidance when needed.
- Presentation abilities.
- Possess a client-oriented approach to work.
- Capable of engaging within a client organisation in a professional manner.
- Agile outlook with respect to work tasks and learning new things.
- Capable of prioritising various duties and accomplish project deadlines.
- Able to think analytically to make independent decisions.
- Keen to work within a matrix setting as well as work well in a ('virtual') team environment.
- Social and communication skills both verbally and in writing.
- To support others to meet study/country deliverables, you will work with a sense of urgency to accomplish allocated duties.
- Capable of managing time efficiently.
- Able to work across cultures.
- High capacity to show commitment to and conduct continuously high-quality work.
- Consulting abilities with a high attention to detail.
- Willing to travel for business needs.
- Possess a full driver's licence where needed.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
LI-GE1
CRODelivery
Clinical
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