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Study Management Associate Jobs in Raleigh, NC (NOW HIRING)

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Site Management Associate I

Raleigh, NC

Site Management Associate I - Amgen NASCR ICON is a global healthcare intelligence and clinical ... Experience in supporting investigator initiated studies Employment with ICON is contingent upon ...

PSI CRO

Site Management Associate I

Durham, NC · On-site

Maintains study-specific and corporate tracking systems * Serves as the sites' primary contact point * Serves as the primary sites' contact point for vendors, study supplies, and access management

PSI CRO

Site Management Associate I

Durham, NC · On-site

Maintains study-specific and corporate tracking systems * Serves as the sites' primary contact point * Serves as the primary sites' contact point for vendors, study supplies, and access management

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Belcan

Clinical Research Associate 3

Durham, NC · On-site

$50.02 - $62.53/hr

Clinical Research Associate 3 Pay Rate: $50.02 - $62.53/hr. Location: Durham, NC ZIP Code: 27701 ... Manager and broader study team on mitigation strategies and follow-up actions. * Collaborate ...

Belcan

Clinical Research Associate 3

Durham, NC

$50.02 - $62.53/hr

Clinical Research Associate 3 Pay Rate: $50.02 - $62.53/hr. Location: Durham, NC ZIP Code: 27701 ... Manager and broader study team on mitigation strategies and follow-up actions. * Collaborate ...

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IQVIA

Trial Delivery Manager, Multi TA

Durham, NC · Remote

... Associate Director, Clinical Trial Management to provide centralized, global clinical trial ... You will lead Study Management Teams (SMTs), oversee country and site-facing activities, and ensure ...

IQVIA

Associate CPM Director

Durham, NC · On-site

Job Overview Manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer ...

New

Pwc

Data Engineer - Senior Associate

Raleigh, NC

$77K - $202K/yr

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

DRMP

Traffic Analysis Project Manager

Raleigh, NC · On-site

Oversee preparation of traffic engineering studies and traffic impact analyses through the life ... Supervises work of Project Managers, Associates, and Interns. * Responsible for personal ...

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All JobsStudy Management Associate JobsStudy Management Associate Jobs in Raleigh, NC

Study Management Associate information

See Raleigh, NC salary details

$10

$39

$56

How much do study management associate jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for study management associate in Raleigh, NC is $39.01, according to ZipRecruiter salary data. Most workers in this role earn between $25.79 and $50.88 per hour, depending on experience, location, and employer.

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

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are the typical responsibilities of a Study Management Associate in a clinical research team?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What is a Study Management Associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.
What are popular job titles related to Study Management Associate jobs in Raleigh, NC? For Study Management Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Study Management Associate jobs in Raleigh, NC look for? The top searched job categories for Study Management Associate jobs in Raleigh, NC are:
Study Management Associate jobs near you
Site Management Associate I

Site Management Associate I

Icon plc

Raleigh, NC

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

Site Management Associate I - Amgen NASCR

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Site Management Associate to join our diverse and dynamic team. As an associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex data, and contributing to the advancement of innovative treatments and therapies.


Key Purpose:
To assist with operational activities, relate to the planning, implementation and execution of Non client Sponsored studies including Investigator Sponsored Studies
(ISS), Co-operative group ISS, Collaborative and Research Development Agreements (CRADAs), Research Partner Studies (RPS), and Expanded Access (EA).

  • Working with other members of the group to support the timely execution and completion of NASCR group deliverables in accordance with standard operating procedures (SOPs) and other supporting documentation

  • Tracks essential documents and files them to the central document repositoryand enters data into source systems

  • Supports execution of operational metrics

  • May be involved in coordination and preparation for meetings (eg, drafting agendas/minutes, scheduling speakers, materials collation)

  • May provide support for numerous other aspects of the process (eg., compiling documents for review submission, budget and contract generation, site initiation packet review and approval, and study close-out)

  • May include creating and monitoring purchase orders, ad hoc administrative projects, and assisting with formatting of presentations.

  • Bachelor's degree in a scientific or healthcare-related field.

  • Prior experience in clinical research support

  • Knowledge of clinical trial processes, regulations, and guidelines.

  • Excellent organizational and communication skills.

  • Ability to work collaboratively in a fast-paced environment with attention to detail.

  • Preferred experience: Experience in supporting investigator initiated studies


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

Apply