Laboratory Technician (PRN)
Evolution Research Group
Summary
The Laboratory Technician is responsible for 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. In executing these position responsibilities, the Clinical Intake Assistant is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, Health Insurance Portability and Accountability Act (HIPAA) and company standard operating procedures and policies.
Job description
Responsibilities
- 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.
- Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.
Skills and Qualifications
- 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.
- Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
- 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)
Requirements
- 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.
- Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
- 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
- Medical coverage
- Dental coverage
- Matching 401(k)
- Paid time off
Company overview
Evolution Research Group is a specialized clinical research organization (CRO) that provides comprehensive clinical trial management and research services to pharmaceutical, biotechnology, and medical device companies. The company focuses on designing, implementing, and managing clinical trials across various therapeutic areas, with particular expertise in complex and specialized medical fields. Their services encompass protocol development, site selection and management, patient recruitment, data management, regulatory compliance, and clinical monitoring. As a CRO, Evolution Research Group plays a critical role in advancing medical research by ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. The organization typically collaborates with research sites, investigators, and sponsors to accelerate the development of new therapies and medical innovations. Their work contributes significantly to the drug development pipeline, helping to bring new treatments from laboratory research to clinical application while maintaining rigorous scientific standards and patient safety protocols.