Senior Clinical Research Associate - Metabolic - Central

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, and together, we are changing the way the world experiences CROs.

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.

About the role

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 work 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 ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment.

In this role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development 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.

Responsibilities

• Manage the research activities at sites participating in Worldwide’s clinical research projects
• Be involved 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 appropriate regulatory documents and supporting the negotiation of contracts and budgets
  • Training sites to collect data properly and report potential safety-related events
  • Managing site activities during study maintenance
  • Closing 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 (most site management efforts will be 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 Metabolic is required; Obesity experience preferred
• Candidates must reside in the Central United States, preferably Texas
• 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.