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Clinical Study Assistant Jobs (NOW HIRING)

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...

The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Study Manager

Durham, NC ยท On-site

$56.99 - $71.32/hr

Job Title: Clinical Study Manager Location: Durham, NC Pay rate: $56.99 - $71.32/hr. Zip Code ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Study Manager

Durham, NC ยท On-site

$56.99 - $71.32/hr

Job Title: Clinical Study Manager Location: Durham, NC Pay rate: $56.99 - $71.32/hr. Zip Code ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Study Manager Location: Durham, NC Duration: 12+ Months Description: The Contract Clinical ... risks. " Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Responsible for securing essential vendor documents for assigned clinical studies to assist in establishing accounts in A/P system within compliance guidelines. * Responsible for establishing ...

Responsible for securing essential vendor documents for assigned clinical studies to assist in establishing accounts in A/P system within compliance guidelines. * Responsible for establishing ...

We understand what clinical study sites need and our overall mission is to support sites in ... visit to assist in a smooth patient flow at research visits., general study conduct tasks ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... risks. * Assist in vendor selection activities, including contribution to RFPs, scopes of work ...

Clinical Trial Associate II

Cambridge, MA ยท On-site

$75K - $90K/yr

Set-up and maintain study clinical trial management system (CTMS) * Assist in development of ... supportive study documents such as informed consent forms, monitoring templates, study subject ...

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Clinical Study Assistant information

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How much do clinical study assistant jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical study assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 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 is a clinical study assistant?

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 are the key skills and qualifications needed to thrive as a clinical study assistant?

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.
More about Clinical Study Assistant jobs
What cities are hiring for Clinical Study Assistant jobs? Cities with the most Clinical Study Assistant job openings:
What are the most commonly searched types of Clinical Study jobs? The most popular types of Clinical Study jobs are:
What states have the most Clinical Study Assistant jobs? States with the most job openings for Clinical Study Assistant jobs include:
Infographic showing various Clinical Study Assistant job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Clinical Lab Assistant

Global Channel Management

Stamford, CT โ€ข On-site

Other

Re-posted 9 days ago


Job description

About the job Clinical Lab Assistant
Clinical Lab Assistant needs 1-2 years of clinical research experience
Clinical Lab Assistant requires:

  • Strong communication skills
  • Flexible and proactive in taking on responsibilities with a willingness to learn
  • Detail oriented
  • Team player, motivated to succeed
  • Flexible schedule 25-30 hours a week
  • Work early mornings or evenings on occasion
  • Excel, PowerPoint, Word
Clinical Lab Assistant duties:
  • Stand for 2-4 hours at a time for execution of clinical studies
  • Assist Clinical Coordinators in preparing and executing clinical studies
  • Prepare documents for clinical studies, assist in study material preparation, interview and administer informed consent to clinical study subjects.
  • Collect data from clinical instrument readings, data entry, quality check of clinical binders, lab preparation before and after study, responsible for assuring large groups of subjects are aware of the study activities, as well as any other information pertinent to them.
  • Communicate instructions effectively.
  • Prepare lab coats, assuring clean laundry for all study needs

Global Channel Management logo

About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

Year founded

2009

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