Senior Clinical Research Associate - Obesity - West Coast - Remote

Worldwide Clinical Trials Holdings, Inc.; Charlotte (NC); Remote; USD 85,000 - 120,000; Full time

Job summary

A leading global CRO is seeking a Senior Clinical Research Associate specializing in Obesity. This remote role involves overseeing clinical research projects, ensuring compliance and safety, and requires strong communication and organizational skills. Ideal candidates will have 5+ years of experience and a relevant degree, contributing to impactful healthcare outcomes.

Qualifications

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

Responsibilities

• Manage research activities at sites for clinical projects.
• Ensure compliance with regulatory requirements and safety reporting.
• Conduct study initiation visits.

Skills

Interpersonal skills

Attention to detail

Organizational skills

Communication skills

Education

4-year university degree or RN/BSN in Nursing

Tools

Microsoft Office

CTMS

EDC systems

Job description

Senior Clinical Research Associate - Obesity - West 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: JR101037

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. 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 their caregivers. From our accessible leaders to our supportive teams, we are committed to enabling success for professionals from all backgrounds. We prioritize a diverse and inclusive environment that promotes collaboration and creativity. 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 impact patients’ lives.

As a Clinical Research Associate (CRA), you will work alongside brilliant minds across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues is ingrained in our culture. We support your professional development with regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

We offer a clear career path towards Clinical Trial Manager roles. Our accessible Executive Leadership team is dedicated to advancing science and surmounting obstacles to make a difference worldwide.

What you will do

1. Manage research activities at sites participating in Worldwide’s clinical research projects, mainly registries and non-interventional/observational studies.
2. Involved in all stages of the clinical study: site identification, start-up activities, regulatory document collection, contract and budget negotiation, site training, safety reporting, site management during study, and study closure.
3. Conduct study initiation visits (SIVs).
4. Ensure compliance with informed consent, safety reporting, and regulatory requirements, mostly remotely.

What you will bring to the role

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

Your experience

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

We love knowing that someone’s work will lead to a better life.

For other roles, visit our careers page or learn more at Worldwide or on LinkedIn.

Worldwide is an equal opportunity employer committed to diversity and inclusion. We value and promote a workplace where everyone feels respected and has equal opportunities.

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