ECN Operating LLC
Job Description
Job Description
Position Summary We are seeking a
highly motivated Research Assistant
to support the day-to-day operations of ongoing clinical trials. This is an excellent opportunity to be a part of a mission-driven team focused on advancing new therapies through rigorous and ethical clinical research. The ideal candidate will bring scientific curiosity, strong organizational skills, and a commitment to quality and compliance. Key Responsibilities Assist in the
design, planning, and execution
of clinical trials in accordance with study protocols. Collect, analyze, and interpret data
from experiments and clinical studies with accuracy and attention to detail. Maintain comprehensive and accurate
research records, logs, and documentation . Collaborate with research coordinators and investigators in preparing
reports, charts, and presentations . Support
laboratory tasks , including tissue and cell culture, assays, and sample handling. Ensure
compliance with FDA regulations, GCP guidelines , and institutional SOPs. Aid in
preparing study-related materials
and coordinating subject visits when necessary. Required Qualifications Bachelor’s degree in
Biology, Life Sciences, Biochemistry, or related field . Prior experience in
clinical trials, biomedical research, or lab work
(preferred). Strong understanding of
molecular biology and cell biology
principles. Familiarity with
FDA regulations and ICH-GCP guidelines . Proficiency in Microsoft Office; experience with
data analysis software (e.g., SAS, R, or Python)
is a plus. Excellent
communication, time management , and organizational skills. High level of accuracy and
attention to detail .
Job Description
Position Summary We are seeking a
highly motivated Research Assistant
to support the day-to-day operations of ongoing clinical trials. This is an excellent opportunity to be a part of a mission-driven team focused on advancing new therapies through rigorous and ethical clinical research. The ideal candidate will bring scientific curiosity, strong organizational skills, and a commitment to quality and compliance. Key Responsibilities Assist in the
design, planning, and execution
of clinical trials in accordance with study protocols. Collect, analyze, and interpret data
from experiments and clinical studies with accuracy and attention to detail. Maintain comprehensive and accurate
research records, logs, and documentation . Collaborate with research coordinators and investigators in preparing
reports, charts, and presentations . Support
laboratory tasks , including tissue and cell culture, assays, and sample handling. Ensure
compliance with FDA regulations, GCP guidelines , and institutional SOPs. Aid in
preparing study-related materials
and coordinating subject visits when necessary. Required Qualifications Bachelor’s degree in
Biology, Life Sciences, Biochemistry, or related field . Prior experience in
clinical trials, biomedical research, or lab work
(preferred). Strong understanding of
molecular biology and cell biology
principles. Familiarity with
FDA regulations and ICH-GCP guidelines . Proficiency in Microsoft Office; experience with
data analysis software (e.g., SAS, R, or Python)
is a plus. Excellent
communication, time management , and organizational skills. High level of accuracy and
attention to detail .