Research Assistant
Columbus, OH · On-site
$20/hr
In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:
Columbus, OH · On-site
$20/hr
In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:
Columbus, OH · On-site
$20/hr
In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:
Columbus, OH · On-site
$19 - $23/hr
In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:
Columbus, OH · On-site
$19 - $23/hr
In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:
... FDA and USDA regulations , ensuring products are accurately labeled, commercially compliant, and successfully brought to market. This role partners closely with R&D, Quality, Packaging, Marketing ...
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... FDA and USDA regulations , ensuring products are accurately labeled, commercially compliant, and successfully brought to market. This role partners closely with R&D, Quality, Packaging, Marketing ...
Coordinates submissions of human subjects research project to the Institutional Review Board (IRB ... Food and Drug Administration (FDA). Essential Functions: * Reviews study protocols in order to ...
Coordinates submissions of human subjects research project to the Institutional Review Board (IRB ... Food and Drug Administration (FDA). Essential Functions: * Reviews study protocols in order to ...
Groveport, OH · On-site
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
Groveport, OH · On-site
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
Groveport, OH · On-site
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
Groveport, OH · On-site
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
Groveport, OH · On-site
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
Groveport, OH · On-site
At KDC, our Research & Development Lab is detail-oriented and hands-on. Be a part of a team making ... Knowledge of FDA GMPs, OSHA safety requirements, SAP, and Microsoft Office. * Strong organizational ...
Columbus, OH · On-site
$27 - $29/hr
Maintain compliance with GCP/GLP guidelines, FDA regulations, and ICH guidelines . * Develop and ... research operations experience within a biotech or healthcare environment. * Experience working in ...
Columbus, OH · On-site
$27 - $29/hr
Maintain compliance with GCP/GLP guidelines, FDA regulations, and ICH guidelines . * Develop and ... research operations experience within a biotech or healthcare environment. * Experience working in ...
$23.50 - $31.25/hr
Clinical Research Coordinator-Hematology Department:Medicine | IM Hematology Clinical Research ... FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with ...
$23.50 - $31.25/hr
Clinical Research Coordinator-Hematology Department:Medicine | IM Hematology Clinical Research ... FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with ...
Columbus, OH · On-site
$22 - $29.25/hr
Clinical Research Coordinator-Hematology Department: Medicine | IM Hematology Clinical Research ... FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with ...
Columbus, OH · On-site
$22 - $29.25/hr
Clinical Research Coordinator-Hematology Department: Medicine | IM Hematology Clinical Research ... FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with ...
Upper Arlington, OH · On-site
$22 - $29.25/hr
Study Planning and Coordination Implements the requirements of clinical research protocols in compliance with local, state, institutional, Federal (FDA, DHHS) and sponsor requirements. Accountable to ...
Upper Arlington, OH · On-site
$22 - $29.25/hr
Study Planning and Coordination Implements the requirements of clinical research protocols in compliance with local, state, institutional, Federal (FDA, DHHS) and sponsor requirements. Accountable to ...
Columbus, OH · On-site
$23.25 - $30.75/hr
Study Planning and Coordination Implements the requirements of clinical research protocols in compliance with local, state, institutional, Federal (FDA, DHHS) and sponsor requirements. Accountable to ...
Columbus, OH · On-site
$23.25 - $30.75/hr
Study Planning and Coordination Implements the requirements of clinical research protocols in compliance with local, state, institutional, Federal (FDA, DHHS) and sponsor requirements. Accountable to ...
Research Associate I INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH ... Ensure strict compliance with GCP and GLP guidelines, FDA regulations, ICH guidelines, and ...
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Research Associate I INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH ... Ensure strict compliance with GCP and GLP guidelines, FDA regulations, ICH guidelines, and ...
... FDA regulations QA process implementation, maintenance and documentation; data entry; and ... Two years clinical research experience or project management experience. Physical Requirements:
... FDA regulations QA process implementation, maintenance and documentation; data entry; and ... Two years clinical research experience or project management experience. Physical Requirements:
... FDA regulations QA process implementation, maintenance and documentation; data entry; and ... Experience Two years clinical research experience or project management experience. Physical ...
... FDA regulations QA process implementation, maintenance and documentation; data entry; and ... Experience Two years clinical research experience or project management experience. Physical ...
Columbus, OH · On-site
$95K - $105K/yr
Ensure compliance with FDA regulations, GMPs, HACCP requirements, labeling regulations, and ... Evaluate research investments and innovation opportunities that deliver long-term value. Represent ...
Columbus, OH · On-site
$95K - $105K/yr
Ensure compliance with FDA regulations, GMPs, HACCP requirements, labeling regulations, and ... Evaluate research investments and innovation opportunities that deliver long-term value. Represent ...
... FDA regulations QA process implementation, maintenance and documentation; data entry; and ... Experience Two years clinical research experience or project management experience. Physical ...
... FDA regulations QA process implementation, maintenance and documentation; data entry; and ... Experience Two years clinical research experience or project management experience. Physical ...
$30K - $42.2K
4% of jobs
$42.2K - $54.5K
3% of jobs
$54.5K - $66.7K
18% of jobs
$67K is the 25th percentile. Wages below this are outliers.
$66.7K - $78.9K
9% of jobs
$78.9K - $91.1K
8% of jobs
$91.1K - $103.4K
3% of jobs
$103.4K - $115.6K
3% of jobs
The median wage is $120.2K / yr.
$115.6K - $127.8K
4% of jobs
$127.8K - $140K
3% of jobs
$140K - $152.3K
3% of jobs
$157.1K is the 75th percentile. Wages above this are outliers.
$152.3K - $164.5K
41% of jobs
$30K
$113.1K
$164.5K
Cities with the most Fda Researcher job openings:
States with the most job openings for Fda Researcher jobs include:

$20/hr
Other
Medical, Dental, Retirement, PTO
Re-posted 23 days ago
About Company:
Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.
Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.
Job Description:
The Research Assistant will ensure compliance with protocol and overall clinical objectives. In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.
Responsibilities:
Skills and Qualifications: