Senior Clinical Research Associate - Respiratory / Rare Disease - Argentina - Remote

Worldwide Clinical Trials; Buenos Aires; Teletrabalho; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

An innovative and dynamic company is seeking a Senior Clinical Research Associate to join their remote team. In this role, you will manage clinical research activities, ensuring quality and compliance while working with diverse teams. Your expertise in pulmonary or respiratory studies will be crucial in driving impactful research that improves patient lives. This organization values creativity and collaboration, fostering an inclusive environment where every team member can thrive. If you are passionate about making a difference in healthcare and have a strong background in clinical research, this opportunity is perfect for you.

Qualificações

• 5+ years of experience as a Clinical Research Associate.
• Experience in Pulmonary or Respiratory required.

Responsabilidades

• Manage research activities at clinical sites for non-interventional studies.
• Conduct study initiation visits and ensure compliance with regulations.

Conhecimentos

Interpersonal Skills

Communication Skills

Organizational Skills

Attention to Detail

Ability to Work Independently

Formação académica

4-year University Degree

RN/BSN in Nursing

Ferramentas

Microsoft Office

CTMS

EDC Systems

Descrição da oferta de emprego

Senior Clinical Research Associate - Respiratory / Rare Disease - Argentina - Remote

Senior Clinical Research Associate - Respiratory / Rare Disease - Argentina - Remote

Apply remote type Remote locations Buenos Aires, Argentina time type Full time posted on Posted 6 Days Ago job requisition id JR100809

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 the Clinical Operations Department does at Worldwide

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can’t get anywhere else, with a team unlike anyone else.

At Worldwide we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.

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:

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Experience in Pulmonary or Respiratory required.
• Willingness to travel required.

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

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.

About Us

This is who we are.

We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever.

We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special.