On-Site Clinical Research Assistant (Entry Level)

Care Access; Mesa (AZ); On-site; USD 26,174 - 45,460; Full time

Benefits offered by this job

Paid Time Off

Company-paid health insurance

Health Savings Account

Flexible Spending Accounts

Employer 401(k) with company match

Job summary

Care Access is hiring an entry-level Clinical Research Assistant to support the Care Access Research process and learn the skills to become a Clinical Research Coordinator. This on-site role offers growth opportunities within the Care Access Research organization and requires the ability to work in a fast-paced environment with protocol-directed tasks.

Key responsibilities include obtaining consent, performing visit procedures, collecting and processing specimens, and maintaining compliance with

Qualifications

• 1 year recent experience as Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.
• Phlebotomy experience and proficiency required.
• Some clinical research experience preferred.

Responsibilities

• Obtain informed consent under CRC direction.
• Complete visit procedures per protocol.
• Collect, process and ship specimens per protocol.
• Maintain FDA/ICH compliance in trials.
• Request study participant payments.
• Schedule visits and reminders.
• Request medical records of potential/current participants.
• Perform basic procedures (blood draws, vitals, ECGs) under CRC
• Update internal trackers and recruitment systems.
• Participate in recruitment phone screenings.
• Assist with outreach materials and participant identification.
• Maintain site logs, inventory, and equipment orders.
• Engage professionally with participants, sponsors, investigators, and staff.

Skills

Independence

Fast learner

Communication skills

Organizational skills

Medical terminology

GCP knowledge

Team player

MS Office

Self-motivation

Positive attitude

Job description

Care Access is hiring an entry-level Clinical Research Assistant to support the Care Access Research process and learn the skills to become a Clinical Research Coordinator. This on-site role offers growth opportunities within the Care Access Research organization and requires the ability to work in a fast-paced environment with protocol-directed tasks.

Key responsibilities include obtaining consent, performing visit procedures, collecting and processing specimens, and maintaining compliance with