Senior Clinical Research Associate

3 settimane fa


Milan, Italia Worldwide Clinical Trials, LLC A tempo pieno
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 Clinical Operations does at Worldwide

Embark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives. Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial.

Working alongside brilliant minds across a variety of therapeutic areas, you will have the chance to collaborate closely with top-tier colleagues from diverse backgrounds and specialties. Our commitment to advancing clinical research is cultivated in a supportive, team-oriented atmosphere, with our hands-on leadership and dedicated team members working together to innovate and solve complex challenges for our customers.

What you will do

Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits

Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data

Actively participate in study team and investigator meetings

Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)

What you will bring to the role

Excellent interpersonal, oral, and written communication skills in English and local language

Superior organizational skills with attention to details, and the ability to work independently

Broad understanding of clinical research principles and process

Proficiency in Microsoft Office, CTMS and EDC Systems

Your experience

At least two years independent clinical monitoring experience

Demonstrable experience of handling multiple protocols across a range of therapeutic indications

Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree)

Ability to meet the travel requirements of the job

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at

www.worldwide.com/careers

For more information on Worldwide, visit

www.Worldwide.com

or connect with us on LinkedIn.

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