Clinical Research Assistant
Actalent, El Paso, TX, United States
Job Title: Clinical Research Assistant
Job Description
This part‑time Research Coordinator role focuses on supporting clinical research studies at a site level in a clinic environment. You will review medical charts, pre‑screen potential study participants, and perform accurate data entry to ensure smooth and compliant study operations. The position offers a long‑term opportunity to contribute to rare disease research within a large site network while working independently within well‑defined study processes.
Responsibilities
Perform detailed medical chart reviews using site‑based, paper source documents to support ongoing clinical research studies.
Conduct pre‑screening activities to identify potential study participants based on study protocols and eligibility criteria.
Complete accurate and timely data entry in electronic data capture (EDC) systems and other study databases.
Support study team members with administrative and research‑related tasks as needed to maintain efficient study operations.
Adhere strictly to study protocols, privacy regulations, and internal procedures to protect participant confidentiality and data integrity.
Collaborate with clinic staff and research team members to ensure consistent and compliant study conduct.
Maintain organized documentation and records to support monitoring, audits, and regulatory requirements.
Work independently within established study workflows while seeking guidance appropriately on complex issues.
Essential Skills
Demonstrated clinical research experience at a study site, specifically in a non‑academic setting.
Hands‑on experience with clinical trials and site‑level study operations.
Proficiency with electronic data capture (EDC) systems and data entry for clinical research.
Experience with patient screening activities in a clinical research context.
Strong attention to detail, particularly when working with paper‑based source documents.
Ability to work independently while following defined study processes and protocols.
Understanding of privacy regulations and the importance of maintaining participant confidentiality.
Work Environment
You will work in a clinic environment that conducts site‑based clinical research, with a focus on paper‑based source documents and electronic data capture systems. This is a part‑time position of approximately 20 hours per week, typically scheduled for 8 hours on Wednesday, 8 hours on Thursday, and 4 hours on Friday. The role requires consistent attention to detail in a structured, process‑driven setting, and you will collaborate closely with a research team while also working independently on assigned tasks. The position offers a long‑term opportunity within a large site network, providing exposure to rare disease studies and specialized therapeutic areas.
Job Type & Location
This is a Contract position based out of El Paso, TX.
Pay and Benefits
The pay range for this position is $20.00 - $25.00/hr.
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long‑term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a hybrid position in El Paso, TX.
Application Deadline
This position is anticipated to close on May 1, 2026.
EEO Statement
Actalent is an equal opportunity employer.
#J-18808-Ljbffr
Job Description
This part‑time Research Coordinator role focuses on supporting clinical research studies at a site level in a clinic environment. You will review medical charts, pre‑screen potential study participants, and perform accurate data entry to ensure smooth and compliant study operations. The position offers a long‑term opportunity to contribute to rare disease research within a large site network while working independently within well‑defined study processes.
Responsibilities
Perform detailed medical chart reviews using site‑based, paper source documents to support ongoing clinical research studies.
Conduct pre‑screening activities to identify potential study participants based on study protocols and eligibility criteria.
Complete accurate and timely data entry in electronic data capture (EDC) systems and other study databases.
Support study team members with administrative and research‑related tasks as needed to maintain efficient study operations.
Adhere strictly to study protocols, privacy regulations, and internal procedures to protect participant confidentiality and data integrity.
Collaborate with clinic staff and research team members to ensure consistent and compliant study conduct.
Maintain organized documentation and records to support monitoring, audits, and regulatory requirements.
Work independently within established study workflows while seeking guidance appropriately on complex issues.
Essential Skills
Demonstrated clinical research experience at a study site, specifically in a non‑academic setting.
Hands‑on experience with clinical trials and site‑level study operations.
Proficiency with electronic data capture (EDC) systems and data entry for clinical research.
Experience with patient screening activities in a clinical research context.
Strong attention to detail, particularly when working with paper‑based source documents.
Ability to work independently while following defined study processes and protocols.
Understanding of privacy regulations and the importance of maintaining participant confidentiality.
Work Environment
You will work in a clinic environment that conducts site‑based clinical research, with a focus on paper‑based source documents and electronic data capture systems. This is a part‑time position of approximately 20 hours per week, typically scheduled for 8 hours on Wednesday, 8 hours on Thursday, and 4 hours on Friday. The role requires consistent attention to detail in a structured, process‑driven setting, and you will collaborate closely with a research team while also working independently on assigned tasks. The position offers a long‑term opportunity within a large site network, providing exposure to rare disease studies and specialized therapeutic areas.
Job Type & Location
This is a Contract position based out of El Paso, TX.
Pay and Benefits
The pay range for this position is $20.00 - $25.00/hr.
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long‑term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a hybrid position in El Paso, TX.
Application Deadline
This position is anticipated to close on May 1, 2026.
EEO Statement
Actalent is an equal opportunity employer.
#J-18808-Ljbffr