Senior Clinical Research Associate - Oncology - Southeast/Mid-Atlantic (Remote)

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 a global team of over 3,500 experts, bright thinkers, dreamers, and doers, working together to change the way the world experiences CROs.

About Us

Our mission is to work with passion and purpose every day to improve lives. 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 a diverse and inclusive environment that fosters collaboration and creativity, where people thrive by being themselves and are inspired to do their best work every day.

About Clinical Operations

At Worldwide Clinical Trials, Clinical Operations invites you to embark on a rewarding journey where your contributions impact patients' lives. As a Clinical Research Associate (CRA), you will collaborate with brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Our supportive, team-oriented environment nurtures advancing clinical research, with extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Regular touchpoints and coaching conversations with your Line Manager ensure your professional development remains a priority. We offer a clear career path leading to Clinical Trial Manager roles and pride ourselves on an accessible Executive Leadership team committed to advancing science and making a difference in patients' lives globally.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Involvement in all stages of the clinical study, including:
  • Identifying potential sites to participate in the research effort.
  • Performing study start-up activities such as collecting regulatory documents and supporting contract and budget negotiations.
  • Training sites on data collection and reporting potential safety-related events.
  • Managing site activities during study maintenance.
  • Closing down research activities at sites once the study concludes.
• Conduct study initiation visits (SIVs).
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, mostly performed remotely.

Requirements

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or Nursing Degree.
• Experience in Oncology is required.
• Candidates must reside in the Southeastern or Mid-Atlantic United States.
• Willingness to travel regionally required.

Pay

The salary range for this position is $97,000.00 - $193,000.00 annually. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location.