Senior Clinical Research Associate - Oncology, Hematology, CNS - Poland
Worldwide Clinical Trials
Virtual PolandFull-time14/8/2026
Role summary
The Senior Clinical Research Associate manages site qualification, initiation, monitoring, and close-out for oncology, hematology, and CNS trials. The role involves mentoring junior staff, ensuring protocol adherence, and maintaining compliance with regulatory standards in a virtual setting.
Full description
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 Neuroscience, Oncology, Cardiovascular, Metabolic 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 site qualification, initiation, interim monitoring, site management, and study close-out visits.
Provide mentoring and guidance to less experienced CRAs and site staff when needed.
Document site visit findings via written reports.
Assess, monitor, and train study site staff on protocol adherence as required.
Review study subject safety information and informed consent.
Conduct source document verification for compliance, patient safety, and veracity of data.
Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
Ensure site compliance with IP receipt, accountability and return or destruction.
Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.
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
Experience in Oncology, Hematology and CNS is required
Willingness to travel required
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 Discover a world of difference at Worldwide! For more information on Worldwide, visit http://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.
Company information
Worldwide Clinical Trials is a global contract research organization (CRO) founded in 1986 by physicians dedicated to advancing medical science. Based in Research Triangle Park, North Carolina, the company operates in over 60 countries with a workforce of more than 2,600 employees. They provide comprehensive clinical development services, covering everything from preclinical research to Phase IV trials and real-world evidence studies.The company offers full-service clinical trial solutions, including early-phase development, late-phase studies, and specialized solutions such as regulatory strategy and cell & gene therapy support. Their expertise spans six core therapeutic areas: rare diseases, cardiovascular and metabolic conditions, oncology, neuroscience, immune-mediated inflammatory diseases, and cell & gene therapy. Worldwide Clinical Trials emphasizes personalized service through therapeutically aligned teams and a robust global infrastructure, ensuring effective trial execution for biotech and pharmaceutical clients.
