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

IQVIA, Inc.

Associate Clinical Lead Director

Durham, NC · On-site

The Associate Clinical Lead Director is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies or a program of studies to meet contractual ...

IQVIA

Associate Clinical Lead Director

Durham, NC

The Associate Clinical Lead Director is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies or a program of studies to meet contractual ...

IQVIA

Associate Clinical Lead Director

Durham, NC

The Associate Clinical Lead Director is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies or a program of studies to meet contractual ...

Wake Research

Clinical Operations Lead

Raleigh, NC · Remote

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential ... Associate degree (2-year program) or equivalent level of education required; Bachelor's Degree (4 ...

M3USA

Clinical Operations Lead

Raleigh, NC · Remote

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential ... Associate degree (2-year program) or equivalent level of education required; Bachelor's Degree (4 ...

M3USA

Clinical Operations Lead

Raleigh, NC · On-site +1

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential ... Associate degree (2-year program) or equivalent level of education required; Bachelor's Degree (4 ...

ICON

Sr. Clinical Research Associate

Raleigh, NC · On-site

Sr. Clinical Research Associate - West ICON is a global healthcare intelligence and clinical ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Alimentiv

Sr. Clinical Operations Lead

Raleigh, NC · Remote

Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... The COL will develop study tools for site and CRA use, review visit reports, review and track ...

Alimentiv

Sr. Clinical Operations Lead

Raleigh, NC

Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... The COL will develop study tools for site and CRA use, review visit reports, review and track ...

M3USA

Clinical Research Site Manager

Raleigh, NC

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential ... Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA) or ...

New

M3USA

Clinical Research Site Manager

Raleigh, NC · On-site

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential ... Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA) or ...

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Clinical Study Associate information

See Raleigh, NC salary details

$12

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$53

How much do clinical study associate jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for clinical study associate in Raleigh, NC is $30.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $40.43 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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 are popular job titles related to Clinical Study Associate jobs in Raleigh, NC? For Clinical Study Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Study Associate jobs in Raleigh, NC look for? The top searched job categories for Clinical Study Associate jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Study Associate jobs? Cities near Raleigh, NC with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Associate Clinical Lead Director

Associate Clinical Lead Director

IQVIA, Inc.

Durham, NC • On-site

Full-time

Posted 13 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

53rd of 203 rated it services

Job description

Job Overview:
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Clinical Lead Director is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies or a program of studies to meet contractual requirements in accordance with (Standard Operating Procedures) SOPs, policies and practices. Associate Clinical Lead Directors ensure clinical delivery to customers, lead clinical teams and partner with Project Leaders and other functional teams to ensure projects meet delivery requirements.
Essential Functions:
  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
  • Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.
  • Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project's lifecycle.
  • Work strategically to realize clinical project goals including setting and developing clinical strategies.
  • Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
  • Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
  • Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
    Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
  • Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
  • Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
  • Conduct regular team meetings and communicate appropriately to achieve objectives.
  • Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.
  • Contribute to the development of the clinical delivery strategy for business proposals.
  • Participate in bid defense preparations and meetings. Develop and present Clinical Operation
  • Plans in partnership with Business Development and Project Leadership.
  • Mentor and coach new peers as they assimilate into clinical lead roles.
  • May act as departmental cross-functional liaison and/or change agent.
  • May attend site visits as applicable in support of project delivery.
  • May participate in, champion and adopt function and/or corporate initiatives, changes and or special project assignments.
  • Travel up to 25%

Qualifications and Requirements:
  • Bachelor's Degree Health care or other scientific discipline Req
  • Requires 10 years clinical research/monitoring experience or equivalent combination of education, training and experience.
  • Requires in-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Requires consolidated knowledge of Project Management practices and terminology.
  • Requires high proficiencies in using systems and technology to achieve work objectives.
  • Requires good knowledge of project finances.
  • Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;
  • Communication - Strong written and verbal communication skills including good command of English language.
  • Problem solving - Problem solving skills.
  • Organization - Planning, time management and prioritization skills.
  • Prioritization - Ability to handle conflicting priorities.
  • Quality - Attention to detail and accuracy in work.
  • Results-oriented approach to work delivery and output.; Leadership - Good influencing and negotiation skills. Good judgment and decision-making skills. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.; including Microsoft Office applications including but not limited to Microsoft Word, Excel
    and PowerPoint.
  • Leadership - Good influencing and negotiation skills. Good judgment and decision-making skills. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.
  • IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel
    and PowerPoint.
  • Collaboration - Ability to establish and maintain effective working.
  • Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
  • IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $102,500.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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