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

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

... • Assist in the development of study documents and tools including informed consent forms ... clinical trial applications, protocols, protocol amendments, clinical study reports and ...

Alimentiv

Clinical Project Manager (US)

Raleigh, NC · Remote

$95K - $159K/yr

Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Alimentiv

Clinical Project Manager (US)

Raleigh, NC · Remote

Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Alimentiv

Clinical Project Manager (US)

Raleigh, NC · On-site +1

$95K - $159K/yr

Applicants should have a minimum of a Bachelor's Degree in a relevant field of study (Health ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

MMS

Senior Medical Writer (Remote)

Raleigh, NC · On-site

... that will assist our clients in developing and marketing life-changing therapies to positively ... Substantial clinical study protocol experience, as lead author, required * Experience leading and ...

UCB

Clinical Development Lead (US)

Raleigh, NC · On-site

... studies. You will balance speed, quality, cost, and complexity, identify risks early, and put ... Should you require any adjustments to our process to assist you in demonstrating your strengths and ...

UCB

Clinical Development Lead (US)

Raleigh, NC · Hybrid

... studies. You will balance speed, quality, cost, and complexity, identify risks early, and put ... Should you require any adjustments to our process to assist you in demonstrating your strengths and ...

AskBio

Director, Pathology

Durham, NC · On-site

The Director, Pathology will provide comprehensive support for nonclinical studies, including primary histopathology and pathology peer reviews, interpretation of all nonclinical study data/findings ...

AskBio

Director, Pathology

Durham, NC · On-site

The Director, Pathology will provide comprehensive support for nonclinical studies, including primary histopathology and pathology peer reviews, interpretation of all nonclinical study data/findings ...

company274

Clinical Research Assistant

Raleigh, NC · On-site

... within study/subject specific windows per protocol guidelines. • Prepare visit-specific ... Clinical Research Coordinator • Observe Coordinator in patient care and management • Assist ...

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Clinical Study Assistant information

See Raleigh, NC salary details

$11

$19

$28

How much do clinical study assistant jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for clinical study assistant in Raleigh, NC is $19.66, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $22.64 per hour, depending on experience, location, and employer.

What are the main challenges a Clinical Study Assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What do clinical trial assistants do?

Clinical Study Assistants support the coordination and administration of clinical trials by preparing documents, scheduling appointments, and ensuring compliance with study protocols. They often handle data entry, assist with patient communication, and maintain trial records under the supervision of study coordinators or investigators. Strong organizational skills and familiarity with clinical trial processes are important for this role.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related healthcare fields. Entry-level roles in clinical research often include Clinical Trial Assistants or Coordinators, with CRAs generally needing several years of experience and relevant certifications such as GCP training.

What are Clinical Study Assistants?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What qualifications do I need to be a clinical research assistant?

A clinical research assistant typically needs a high school diploma or equivalent, with some roles preferring a bachelor's degree in health sciences, biology, or a related field. Relevant skills include attention to detail, organizational abilities, and familiarity with clinical trial protocols and data management tools. Certification in Good Clinical Practice (GCP) or clinical research fundamentals can enhance job prospects.

Is CRA better than CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are different roles in clinical trials. CRAs typically oversee multiple sites, monitor study progress, and ensure compliance, often requiring travel and certification. CRCs manage day-to-day trial activities at a single site, including patient interactions and data collection, usually working regular hours. Both roles are essential, but they focus on different aspects of clinical research.

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

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation 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:
Clinical Study Assistant jobs near you
Clinical Study Lead

Clinical Study Lead

Advanced Recruiting Partners

Raleigh, NC • On-site

Other

Posted 14 days ago

Job description

Job Summary:

The Study Lead will oversee the planning, execution, and management of clinical trials from start to finish. This role involves coordinating study activities, ensuring compliance with regulatory requirements, and leading a team of CRAs while collaborating closely with cross-functional teams. The ideal candidate will have a strong background in clinical trial management and a passion for advancing medical research.


Key Responsibilities:

  • Lead the planning, execution, and management of clinical trials in accordance with GCP, regulatory guidelines, and company SOPs.
  • Develop and manage study protocols, informed consent forms, and other essential study documentation.
  • Serve as the primary point of contact for all study-related inquiries and issues.
  • Coordinate with site personnel, vendors, and internal teams to ensure smooth study execution.
  • Monitor study progress and conduct regular reviews of study data to ensure integrity and compliance.
  • Provide training and mentorship to CRAs and other study team members.
  • Assist in the selection and evaluation of clinical sites and vendors.
  • Prepare and present study updates to senior management and stakeholders.
  • Participate in regulatory submissions and inspections as needed.
  • Identify and mitigate study-related risks proactively.


Qualifications:

  • Bachelor’s degree in life sciences or a related field; advanced degree preferred.
  • Minimum 3 years of experience in clinical trial management or CRA role, preferably in a biotech environment.
  • Strong understanding of clinical trial regulations and Good Clinical Practice (GCP).
  • Excellent organizational and project management skills.
  • Strong interpersonal and communication skills, with the ability to work collaboratively in a team-oriented environment.
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Ability to work independently and adapt to changing priorities in a fast-paced environment.

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