Jersey City, NJ · On-site
Associate degree or higher preferred Experience: 1-2 year relevant experience in pharmaceutical industry or CRO Experience supporting clinical trials preferred Qualifications Knowledge, Skills, and ...
Jersey City, NJ · On-site
Associate degree or higher preferred Experience: 1-2 year relevant experience in pharmaceutical industry or CRO Experience supporting clinical trials preferred Qualifications Knowledge, Skills, and ...
Study Start-Up Support: • Assist with the development of clinical trial materials, e.g. trial master file build, patient binders, filing. • Assist the clinical team with the organisation and ...
Study Start-Up Support: • Assist with the development of clinical trial materials, e.g. trial master file build, patient binders, filing. • Assist the clinical team with the organisation and ...
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based administrative assistant to join our Clinical Monitoring Training & Development team in ...
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based administrative assistant to join our Clinical Monitoring Training & Development team in ...
Weinkauf's research trial; responsible for completing intake for patients and meeting IRB ... for clinical trial; assist senior lab members with submitting required documentation to IRB.
Weinkauf's research trial; responsible for completing intake for patients and meeting IRB ... for clinical trial; assist senior lab members with submitting required documentation to IRB.
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based administrative assistant to join our Clinical Monitoring Training & Development team in ...
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based administrative assistant to join our Clinical Monitoring Training & Development team in ...
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Track study progress and generate routine status reports and metrics as requested * Assist with ...
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Track study progress and generate routine status reports and metrics as requested * Assist with ...
Manhattan, NY · On-site
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Track study progress and generate routine status reports and metrics as requested * Assist with ...
Manhattan, NY · On-site
$36.75 - $50.25/hr
The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Track study progress and generate routine status reports and metrics as requested * Assist with ...
Marlton, NJ · On-site
$95K - $115K/yr
Support all activities related to clinical trial oversight committees (Steering Committee, DSMB, Clinical Events Committee). * Assist with CRA and third-party vendor training on protocols and ...
Marlton, NJ · On-site
$95K - $115K/yr
Support all activities related to clinical trial oversight committees (Steering Committee, DSMB, Clinical Events Committee). * Assist with CRA and third-party vendor training on protocols and ...
Blue Bell, PA · On-site
Clinical Trial Liaison 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 ...
Blue Bell, PA · On-site
Clinical Trial Liaison 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 ...
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... * Assist in collecting and completing essential study-related activities, including data entry ...
Quick apply
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... * Assist in collecting and completing essential study-related activities, including data entry ...
Needham, MA · On-site
$88 - $100/hr
... * Assist in collecting and completing essential study‑related activities, including data entry ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Needham, MA · On-site
$88 - $100/hr
... * Assist in collecting and completing essential study‑related activities, including data entry ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... * Assist in collecting and completing essential study-related activities, including data entry ...
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... * Assist in collecting and completing essential study-related activities, including data entry ...
Blue Bell, PA · On-site
Clinical Trial Liaison 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 ...
Quick apply
Blue Bell, PA · On-site
Clinical Trial Liaison 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 ...
Needham, MA · On-site
$88 - $100/hr
... * Assist in collecting and completing essential study‑related activities, including data entry ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Needham, MA · On-site
$88 - $100/hr
... * Assist in collecting and completing essential study‑related activities, including data entry ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
San Diego, CA · On-site +1
$140K - $178K/yr
The Senior/Clinical Trial Manager will be responsible for managing and executing operational ... Support clinical sites in preparation for audits and inspections. * Assist with budget management ...
Quick apply
San Diego, CA · On-site +1
$140K - $178K/yr
The Senior/Clinical Trial Manager will be responsible for managing and executing operational ... Support clinical sites in preparation for audits and inspections. * Assist with budget management ...
Boston, MA · Hybrid
$120K - $150K/yr
... Assist with oversight of CRO and vendor set-up, liaising with CROs to ensure timely study ... Coordinate Clinical Trial Team meetings and drive action item follow-up. Maintain clinical ...
Boston, MA · Hybrid
$120K - $150K/yr
... Assist with oversight of CRO and vendor set-up, liaising with CROs to ensure timely study ... Coordinate Clinical Trial Team meetings and drive action item follow-up. Maintain clinical ...
Raleigh, NC · On-site
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...
Raleigh, NC · On-site
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...
Newark, CA · On-site
$86K - $105K/yr
Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...
Newark, CA · On-site
$86K - $105K/yr
Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
A clinical trial assistant is responsible for monitoring the medical and administrative procedures during a clinical trial. In this career, you prepare patients for tests, take blood, perform laboratory work, prep for medical treatments, and collect data for research. You work with project managers and research associates throughout the beginning, implementation, and closeout of the trial. You also handle paperwork, file records, prepare reports, label medication, track progress, and fulfill other duties that arise during medical studies. You may assist with appointment schedules, plan meetings, and communicate with external sources and investigators as well.
| Aspect | Clinical Trial Assistant | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Supports trial logistics, manages documentation, assists with regulatory compliance | Oversees study conduct, recruits participants, manages site operations |
| Credentials | Typically requires a bachelor's degree in health or life sciences | Often requires a bachelor's or master's degree in health sciences or related fields |
| Work Environment | Research sites, sponsor offices, clinical trial centers | Clinical sites, hospitals, research institutions |
| Industry Usage | Commonly employed in pharmaceutical companies, CROs, research institutions | Primarily in hospitals, clinics, research centers |
The Clinical Trial Assistant primarily supports trial logistics and documentation, working closely with the research team. In contrast, the Clinical Research Coordinator manages the overall conduct of the study, including participant recruitment and site management. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.
Cities with the most Clinical Trial Assistant job openings:
The most popular types of Clinical Trial jobs are:
The top employers for Clinical Trial Assistant jobs are:
States with the most job openings for Clinical Trial Assistant jobs include:
The top searched job categories for Clinical Trial Assistant jobs are:
For Clinical Trial Assistant jobs, the most frequently searched job titles are:
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.
Associate degree or higher preferred
Experience:
1-2 year relevant experience in pharmaceutical industry or CRO
Experience supporting clinical trials preferred
Knowledge, Skills, and Abilities
Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus
Proficiency with Microsoft Word, Microsoft PowerPoint, Microsoft Outlook, and Adobe Acrobat
Strong skills with Microsoft Excel required
Experience using electronic data capture (EDC) systems is a plus
To know more on this position or to schedule an interview, please contact;
Sagar Rathore
630-485-2166
sagar.rathore[@]collabera.com
Sourced by ZipRecruiter
Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data/AI. With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.
It services
5,001 - 10,000 Employees
Morristown, NJ, US
