In-House Clinical Research Associate

4 settimane fa

Milano, Italia Worldwide Clinical Trials A tempo pieno

**Requisition Number**7638**
**Employment 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 heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
**Why Worldwide**
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us
**What you will do**
- Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
- Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)
- Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
- Perform feasibility studies/site identification activities for potential sites, as requested
**What you will bring to the role**
- Excellent interpersonal, oral, and written communication skills in English and proficiency in one of the following languages
- Italian, German, Spanish or French
- Ability to contribute to a team remotely
- Strong customer focus, ability to interact professionally with a sponsor contact
- Proficiency in Microsoft Office, CTMS, and EDC Systems
**Your experience**
- Four-year college curriculum with a major concentration in life science preferred but not required, OR
- Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant
We love knowing that someone is going to have a better life because of the work we do.
LI-MZ1

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