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Clinical Trials Jobs in Raleigh, NC (NOW HIRING)

Worldwide Clinical Trials

Senior Statistician

Durham, NC

$84K - $103K/yr

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 ...

Worldwide Clinical Trials

Senior Statistician

Durham, NC · On-site +1

$84K - $103K/yr

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 ...

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Clinical Trials information

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$28

$60

$93

How much do clinical trials jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical trials in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

What are some common career paths or advancement opportunities for professionals working in clinical trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

What is a clinical trial?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are the most commonly searched types of Clinical Trials jobs in Raleigh, NC? The most popular types of Clinical Trials jobs in Raleigh, NC are:
What are popular job titles related to Clinical Trials jobs in Raleigh, NC? For Clinical Trials jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Trials jobs in Raleigh, NC look for? The top searched job categories for Clinical Trials jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Trials jobs? Cities near Raleigh, NC with the most Clinical Trials job openings:
Clinical Trials jobs near you
Infographic showing various Clinical Trials job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 17% Part Time, and 9% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Cardiology Physician Noninvasive Cardiologist - Physicians Only Apply - Perm

Worldwide Clinical Trials

Raleigh, NC

$316K - $357K/yr

Full-time

Re-posted 4 days ago

Job description

Medical Doctors Only Apply. A Cardiology Physician Noninvasive Cardiologist practice is seeking a qualified physician for Raleigh, NC. This and other physician jobs brought to you by ExactMD.

Worldwide Clinical Trials is the cure of the common CRO.  The time is right to join our growing team, consisting of 1,600 talented and dedicated employees from across the globe. We’re doing innovative and exceptional work each and every day. Our team is filled with purpose, as we support our sponsors in the discovery of cures and treatments for diseases affecting millions of people around the world.

If you’re looking to join an energetic and collaborative team that is valued and supported by company leadership, committed to operational excellence and open to creativity and innovation, Worldwide Clinical Trials could be the ideal place for you. We have exciting opportunities in clinical drug development, project management, corporate functions, sales, and more. Explore current openings and learn more about Worldwide’s culture below.

We are looking for a Sr. Medical Director to join our team.  This Cardiologist will provide medical management and professional medical support for clinical research projects at WCT as the assigned Medical Monitor (MM). To assist in activities requiring Medical & Scientific support, including but not limited to: assistance with feasibility assessments, medical training and provision of medical/clinical input to the design of study protocols and/or clinical development programs as well as assistance with business development activities, as directed by the department head.

RESPONSIBILITIES:

Tasks may include but are not limited to:

ï‚· Medically manages clinical trials to which s/he is assigned as MM

ï‚· Serves as Global Lead MM (GLMM) for pan-regional and/.or global trial(s) to which s/he is assigned

ï‚· Collaborates with the other members of the Medical & Safety project team to process Serious Adverse Events (SAEs)

US: when contracted might conducts and document an Analysis of Similar Events (AOSE) included as part of the case narrative, in keeping with FDA 21CFR312.32

ï‚· Provides therapeutic and protocol-specific training to the project teams

ï‚· Contributes medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc

ï‚· Provides after hours medical support for projects to which s/he is assigned

ï‚· Independently supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management

ï‚· Reviews and/or assist in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc,) as directed by senior management

ï‚· Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc) , review of relevant therapeutic/clinical literature and attendance in conferences and meetings

ï‚· Interacts with staff in other functional areas within the company to ensure the highest level of client satisfaction through successful execution of projects

ï‚· Identifies, documents and appropriately resolves out-of-scope work as directed by senior management

ï‚· Assists in the annual attainment of departmental revenue targets and any other activities as directed by senior management

ï‚· Maintains working knowledge of GCPs and regulatory requirements relating to clinical development and safety assure compliance with ethical, legal and regulatory standards

 Mentors other medical staff as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, support Senior Management’s leadership of both the department and the company.

REQUIREMENTS:

ï‚· Customary office desk and managerial work, no heavy lifting, occasional business travel

ï‚· Medical Degree from an accredited institution of Medical Education.

ï‚· 6-8 years clinical research or industry experience

Apply