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Clinical Study Manager Jobs in Raleigh, NC (NOW HIRING)

Sr Clinical Trials Manager

Raleigh, NC ยท On-site

$143.23K - $185.35K/yr

Works with management on departmental issues, providing input to clinical operations strategies and ... Ability to write study protocols, study reports, sections for investigator brochures, and ...

The study management team is collectively responsible for planning, solutioning, recruiting, executing, and close-out of clinical studies, within the scope of the client agreement. In doing so, the ...

The study management team is collectively responsible for planning, solutioning, recruiting, executing, and close-out of clinical studies, within the scope of the client agreement. In doing so, the ...

... clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned - * Responsible for all aspects of site management as ...

Clinical Project Manager (US)

Raleigh, NC ยท Remote

$95.50K - $159K/yr

Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health Sciences, Clinical Research preferred) and 1-3 years of experience in clinical study management * The ...

Clinical Project Manager (US)

Raleigh, NC ยท On-site +1

$95.50K - $159K/yr

Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health Sciences, Clinical Research preferred) and 1-3 years of experience in clinical study management * The ...

Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health Sciences, Clinical Research preferred) and 1-3 years of experience in clinical study management * The ...

Project Manager, II Labs- hybrid ICON is a global healthcare intelligence and clinical research ... Prepare and QC clinical study specific materials. * Ensure that proper guidelines for communication ...

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Clinical Study Manager information

See Raleigh, NC salary details

$28

$60

$93

How much do clinical study manager jobs pay per hour?

As of May 31, 2026, the average hourly pay for clinical study manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.28 and $68.46 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Study Manager, and why are they important?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by Clinical Study Managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

What does a Clinical Study Manager do?

A Clinical Study Manager oversees the planning, execution, and management of clinical trials to ensure they meet regulatory, ethical, and scientific standards. They coordinate with cross-functional teams, manage timelines and budgets, and ensure compliance with protocols and regulations. Their responsibilities also include selecting study sites, overseeing data collection, and maintaining communication with stakeholders. Ultimately, they play a crucial role in ensuring the success and integrity of clinical research studies.
What are the most commonly searched types of Clinical Study jobs in Raleigh, NC? The most popular types of Clinical Study jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Study Manager jobs? Cities near Raleigh, NC with the most Clinical Study Manager job openings:
Senior Clinical Trial Manager - CNS - U.S. - Remote

Senior Clinical Trial Manager - CNS - U.S. - Remote

Worldwide Clinical Trials

Durham, NC โ€ข On-site, Remote

Full-time

Posted 3 days ago


Job description

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, and 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 - 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 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.Join us!

What Clinical Operations Site Management does at Worldwide

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role in every clinical trial. All CROs will promise you growth, opportunity, and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can't get anywhere else, with a team unlike anyone else.

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient's life depends on it - because it does.Our leaders are in the trenches with you, committed to advancing science and moving mountains for our customers.

What you will do

  • Provide leadership and direction to clinical site management team members from study start through to closure

  • Serve as Site Management's primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to

  • Primary Sponsor Contact

  • Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English

  • Ability to lead and motivate ateam remotely

  • Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified

  • Strong customer focus, ability to interact professionally with a sponsor contact

  • Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

  • Bachelor's Degree or a Nursing Degree required

  • 1+ years' experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role

  • 3+ years' experience as a Clinical Research Associate

  • CNS/Neurologyexperience isrequired

  • Willingness to travel up to 30%

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.