Senior Clinical Research Associate - Obesity - East Coast - Remote

Worldwide Clinical Trials Holdings, Inc.; Charlotte (NC); Remote; USD 70,000 - 90,000; Full time

Job summary

A global CRO is seeking a Senior Clinical Research Associate to manage clinical research in obesity, primarily remotely. Responsibilities include overseeing site activities, ensuring regulatory compliance, and collaborating with diverse teams. Ideal candidates possess 5+ years of clinical research experience and strong communication skills, ready to contribute to impactful projects.

Qualifications

• 5+ years as a Clinical Research Associate.
• Experience in Obesity is required.
• Reside on the East Coast of the United States.

Responsibilities

• Manage research activities at clinical sites, primarily registries and observational studies.
• Involved in all stages of clinical studies including site training and safety reporting.
• Conduct study initiation visits (SIVs) and ensure regulatory compliance.

Skills

Interpersonal communication

Organizational skills

Detail-oriented

Independent work

Proficiency in English

Education

4-year university degree or RN/BSN in Nursing

Tools

Microsoft Office

CTMS

EDC systems

Job description

Senior Clinical Research Associate - Obesity - East Coast - Remote

Apply remote type: Remote | Locations: Research Triangle Park, North Carolina | Time type: Full time | Posted on: Posted 5 Days Ago | Job requisition id: JR101035

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, a global team of over 3,500+ experts, bright thinkers, dreamers, and doers, 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 difference for patients and caregivers. From our accessible leaders to our cohesive teams, we are committed to enabling professionals from all backgrounds to succeed. We prioritize a diverse and inclusive environment that promotes 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

In Clinical Operations, your contributions will impact patients’ lives. As a CRA, you will work alongside brilliant minds across therapeutic areas like Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration is ingrained in our culture, supported by regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

We support your professional development through regular touchpoints and coaching, with clear career paths leading to Clinical Trial Manager roles. Our accessible leadership is committed to scientific advancement and overcoming obstacles to improve patient lives worldwide.

What you will do

• Manage research activities at sites participating in Worldwide’s clinical research projects, primarily registries and observational studies.
• Involved in all stages of the clinical study, including site identification, start-up activities, regulatory document collection, contract and budget support, site training, safety reporting, study maintenance, and site closure.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent, safety reporting, and regulatory requirements, mostly remotely but with some site visits.

What you will bring to the role

• Excellent interpersonal, oral, and written English communication skills.
• Superior organizational skills with attention to detail.
• Ability to work independently.
• Proficiency in Microsoft Office, CTMS, and EDC systems.

Your experience

• 5+ years as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Experience in Obesity is required.
• Reside on the East Coast of the United States.
• Willingness to travel.

We love knowing our work improves lives. For other roles, visit our careers page at Discover a world of difference at Worldwide. For more information, visit www.Worldwide.com or connect on LinkedIn.

Worldwide is an equal opportunity employer committed to diversity, inclusion, and equal access for all employees and applicants, regardless of race, ethnicity, gender, age, disability, or other protected status.