Clinical Research Assistant

Tribe Clinical Research; Greenville (SC); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Excellent PTO including birthday leave

7 paid holidays

401K

Scrubs stipend

Monthly phone stipend

Office amenities

Job summary

Tribe Clinical Research in Greenville, SC is seeking an experienced Clinical Research Assistant to support Coordinators and Principal Investigators in Phase II–IV trials, ensuring regulatory compliance and high-quality data handling. The role requires an outgoing, friendly personality and someone who enjoys working with a diverse population.

Key duties include data entry, patient relations, scheduling, and sponsor communications, with CMA certification preferred or willingness to complete.

Qualifications

• CMA certification or willingness to complete.
• Familiarity with medical and clinical research terminologies.
• Exceptional attention to detail and accuracy.
• Data management and informatics knowledge.
• Adherence to ethical research standards.
• Highly organized with ability to multitask.
• Willingness to engage in continuous learning.

Responsibilities

• Obtain various samples as necessary.
• Detailed record keeping, data entry, and verification.
• Medical record review and protocol documentation.
• Patient relations and sponsor communications.
• Scheduling and coordination with study sites.

Skills

CMA Certification

Medical terminology

Attention to detail

Data management

Ethical research

Highly organized

Continuous learning

Job description

Thank you for your interest in this posting!

Tribe Clinical Research is seeking an experienced and highly organized Clinical Research Assistant.The Clinical Research Assistant will assist Clinical Research Coordinators and Principal Investigators in conducting Phase II, III, and IV clinical trials within internationally accepted standards of knowledge and understanding of the research process and related regulations.Since this is primarily a customer contact position, it requires an outgoing, friendly personality and someone who enjoys working with a diverse population of people.

Key Skills and Competencies:

• CMA Certification or willingness to complete
• Medical and Clinical Research Terminologies
• Exceptional attention to detail and accuracy
• Data Management and Informatics
• Adhere to Principles of Ethical Research Standards
• Highly organized individual
• Continuous learning mindset

Primary Accountabilities:

• Obtain various samples, as necessary
• Detailed record keeping, data entry, and verification
• Medical Record Review
• Protocol compliance/documentation
• Patient relations
• Sponsor relations/communication
• Scheduling

Physical Requirements

This position may require travel, lifting (up to 50 pounds), sitting, standing, and walking associated with a normal clinical research/physician office environment. A person in this position may be exposed to fumes, airborne particles, infectious diseases, blood/bodily fluids, and disease-bearing specimens.

A note about Tribe Clinical Research: Tribe Clinical Research

is an independent, faith-based, clinical research facility that conducts both adult and pediatric research studies.Our purpose is to provide hope for the future by unlocking the potential of medicine.

Our culture is centered around our core values:

• We are passionate about working for a GROWTH-ORIENTED company.
• We exhibit a HUMBLE but CONFIDENT approach to work.
• We communicate RESPECTFULLY.
• We love serving others and WORKING TOGETHER for the greater good.
• We can take constructive feedback well and have a POSITIVE ATTITUDE.

Other benefits:

• Excellent PTO plan including your birthday day off
• 7 paid holidays
• 401K
• $150 stipend towards new scrubs
• Monthly Phone Stipend
• Office amenities (coffee, snacks, water)
• An amazing team to work with

Tribe Clinical Research is an Equal Opportunity Employer