Clinical Research Associate - Italy - Remote

worldwide.com; Roma; Ibrido; EUR 42.000 - 56.000; Tempo pieno

Descrizione del lavoro

Worldwide Clinical Trials is seeking a Clinical Research Associate for Italy (Rome) with remote work options. The role supports diverse therapeutic areas, including regulatory submissions and TMF management, with extensive collaboration across global teams.

You will manage site-related activities, perform SIVs, and ensure compliance with regulatory requirements while traveling as needed. Excellent English and strong organizational skills are essential.

Competenze

• 2+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• English-language communication skills.
• Proficiency in Microsoft Office, CTMS and EDC systems.
• Ability to work with minimal supervision.
• Willingness to travel.

Mansioni

• Manage research activities at sites participating in Worldwide’s projects, mainly registries/non-interventional studies.
• Identify prospective sites and perform start-up activities, including regulatory documents and budget negotiations.
• Train sites to collect data accurately and report safety events.
• Oversee site activities during study maintenance and close-out.
• Conduct study initiation visits (SIVs).
• Ensure informed consent and regulatory compliance in remote settings.

Conoscenze

Interpersonal skills

English proficiency

Organizational skills

Self-motivation

MS Office

CTMS

EDC systems

Formazione

4-year university degree or RN/BSN in Nursing

Strumenti

CTMS

EDC systems

MS Office

Descrizione del lavoro

## Clinical Research Associate - Italy - RemoteApplyremote type: Remotelocations: Rome, Italytime type: Full timeposted on: Posted 30+ Days Agojob requisition id: JR101971**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.**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**At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.**What you will do*** Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies* Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded* Conduct study initiation visits (SIVs)* While most of the site management efforts will be performed remotely, will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements**What you will bring to the role*** Excellent interpersonal, oral, and written communication skills in English* Superior organizational skills with attention to details* Ability to work with little or no supervision* Proficiency in Microsoft Office, CTMS and EDC Systems**Your experience*** 2+ years of experience as a Clinical Research Associate* 4-year university degree or RN/BSN in Nursing* **Please submit English resume*** Willingness to travel requiredWe 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 Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law**.**