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Evolution Research Group

Laboratory Technician

Evolution Research Group

Laboratory Technician assisting with clinical trials, document management, and laboratory functions for Evolution Research Group. Collaborating with clinical teams and maintaining accurate participant documentation.

Posted 7/16/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $22 - $27 per hourWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates proficiency in clinical skills such as Phlebotomy, Vital Sign Measurements, and ECGs, while ensuring compliance with Good Clinical Practices (GCP) and regulatory requirements. Strong organizational and communication skills are essential for effective collaboration with clinical research teams and maintaining accurate documentation.

Highest-signal resume keywords
PhlebotomyVital Sign MeasurementsGood Clinical Practices (GCP)Electronic Data CaptureMedical Terminology

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
PhlebotomyVital Sign MeasurementsECGsData EntrySafety AssessmentsDemographic CollectionMedical History CollectionAttention to DetailRegulatory ComplianceClinical Assessments
Soft Skills
Interpersonal SkillsOrganizational SkillsCommunication SkillsCustomer ServiceCollaboration
Tools & Technologies
WordExcelStudy ManagerElectronic Data Capture Platforms
Certifications & Qualifications
Medical Assistant CertificationCNA Certification
Industry Keywords
Clinical TrialsGood Clinical Practices (GCP)International Conference of Harmonization (ICH)Site Standard Operating ProceduresClinical Research

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Assisting with document management, protocol related clinical assessments of research subjects, laboratory functions, and assisting in tasks of the Clinical Research Coordinators as it relates to the conduct of clinical trials.
  • Completes all duties under the direction of the Site Director or designee.
  • Maintains accurate, confidential files and documentation of study participants.
  • Maintain tenants of good customer service when interacting with subjects, staff, and representatives of sponsors or CROs.
  • Clinical skills include phlebotomy, vital sign measurements, and performing ECGs.
  • Collect demographic, medical, and medication history.
  • Complete safety assessments
  • Work closely and collaboratively with Director of Clinical Operations, Clinical Research Coordinators, Sub-Investigator, and Principal Investigator.
  • Enter data as appropriate for multiple Electronic Data Capture platforms as well as respond and resolve queries that may arise.
  • Meet defined goals established in conjunction with site leadership.
  • Study, learn, and comply with ERG site standard operating procedures, and other policies, practices, and regulations where applicable.

Requirements

What you’ll need
  • High School Diploma or equivalent
  • Experience in a medical setting/ training and certification as a Medical Assistant/CNA
  • Understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
  • Good organizational and interpersonal skills
  • Attention to detail.
  • Knowledgeable in medical terminology
  • Excellent communication skills (interpersonal, written, verbal)
  • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

Benefits

Comp & perks
  • medical and dental coverage
  • matching 401(k)
  • paid time off