About this role
At Worldwide Clinical Trials, we are 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. As a Senior Clinical Research Associate specializing in Oncology, you will join a team of over 3,500 experts, bright thinkers, dreamers, and doers who are changing the way the world experiences CROs.
In this role, you will be responsible for managing research activities at sites participating in Worldwide's clinical research projects, with a focus on Oncology trials. You will be involved in all stages of the clinical study, from identifying potential sites and performing study start-up activities to training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research at study conclusion.
While most site management efforts will be performed remotely, you will ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements. You will work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases, within a supportive and team-oriented environment.
Through regular touchpoints and coaching conversations with your Line Manager, your professional development remains a top priority, with a clear career path that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
Requirements
- Excellent organizational and site management skills
- Experience managing clinical research sites in the pharmaceutical or CRO industry
- Oncology therapeutic area experience is strongly preferred
- Ability to perform remote site management while ensuring regulatory compliance
- Proficiency in collecting and reviewing regulatory documents
- Experience conducting study initiation visits (SIVs)
- Knowledge of ICH-GCP guidelines and applicable regulatory requirements
Responsibilities
- Manage research activities at sites participating in Worldwide's clinical research projects, with a focus on Oncology trials
- Identify potential sites to participate in the research effort and perform study start-up activities
- Work with sites to collect appropriate regulatory documents and support the negotiation of contracts and budgets
- Train sites to collect data properly and report any potential safety-related events
- Manage site activities during study maintenance and close down research activities at sites once the study has concluded
- Conduct study initiation visits (SIVs)
- Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
Benefits
- Supportive and team-oriented environment with collaboration across diverse therapeutic areas
- Regular touchpoints and coaching conversations with your Line Manager to prioritize professional development
- Clear career path with potential to advance to Clinical Trial Manager roles
- Accessible Executive Leadership team committed to advancing science and overcoming obstacles
- Remote work flexibility with a focus on site management from home
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