IRB Coordinator
Robert Lee, TX · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
Robert Lee, TX · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
Robert Lee, TX · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
Robert Lee, TX · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
Robert Lee, TX · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
Addis, LA · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
Addis, LA · On-site
... seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects ... Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft ...
$135 - $175/hr
About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Support hospital IRB processes and vendor vetting procedures * Lead clinical training and education ...
$135 - $175/hr
About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Support hospital IRB processes and vendor vetting procedures * Lead clinical training and education ...
New York, NY · On-site
$45K - $50K/yr
No We invite applications for a Research Scientist Program Manager (Part-Time, Postdoctoral Level ... Coordinate IRB submissions/renewals, reliance agreements, and other research compliance ...
New York, NY · On-site
$45K - $50K/yr
No We invite applications for a Research Scientist Program Manager (Part-Time, Postdoctoral Level ... Coordinate IRB submissions/renewals, reliance agreements, and other research compliance ...
New York, NY · On-site +1
$45K - $50K/yr
No We invite applications for a Research Scientist Program Manager (Part-Time, Postdoctoral Level ... Coordinate IRB submissions/renewals, reliance agreements, and other research compliance ...
New York, NY · On-site +1
$45K - $50K/yr
No We invite applications for a Research Scientist Program Manager (Part-Time, Postdoctoral Level ... Coordinate IRB submissions/renewals, reliance agreements, and other research compliance ...
Location BMH Bronson Methodist Hospital Title Nursing Research Program Manager (RN) Part-Time This ... Assistin developing research protocols, IRB submissions, and regulatory documentation.
Location BMH Bronson Methodist Hospital Title Nursing Research Program Manager (RN) Part-Time This ... Assistin developing research protocols, IRB submissions, and regulatory documentation.
Location BMH Bronson Methodist Hospital Title Nursing Research Program Manager (RN) Part-Time ... Assistin developing research protocols, IRB submissions, and regulatory documentation.
Location BMH Bronson Methodist Hospital Title Nursing Research Program Manager (RN) Part-Time ... Assistin developing research protocols, IRB submissions, and regulatory documentation.
Location BMH Bronson Methodist Hospital Title Nursing Research Program Manager (RN) Part-Time ... Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation ...
Location BMH Bronson Methodist Hospital Title Nursing Research Program Manager (RN) Part-Time ... Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation ...
Dayton, OH · On-site
$16/hr
The Research Program Assistant will provide sustained coordination, data management, and compliance ... Familiarity with IRB processes and human subjects research. * Experience with qualitative or mixed ...
Dayton, OH · On-site
$16/hr
The Research Program Assistant will provide sustained coordination, data management, and compliance ... Familiarity with IRB processes and human subjects research. * Experience with qualitative or mixed ...
Philadelphia, PA · On-site
$19.50 - $26.75/hr
Research Assistant Job no: 506856 Work type: Part-Time Location: University City - Philadelphia, PA ... with IRB management and submissions Required Qualifications * Minimum of a Master's Degree in ...
Philadelphia, PA · On-site
$19.50 - $26.75/hr
Research Assistant Job no: 506856 Work type: Part-Time Location: University City - Philadelphia, PA ... with IRB management and submissions Required Qualifications * Minimum of a Master's Degree in ...
Manhattan, NY · On-site
$48 - $52/hr
Certified Clinical Research Coordinator (CCRC) Part-Time | One Day per Week (On-Site) Location ... and manage assigned clinical trials in compliance with GCP, ICH, FDA regulations, and IRB ...
Quick apply
Manhattan, NY · On-site
$48 - $52/hr
Certified Clinical Research Coordinator (CCRC) Part-Time | One Day per Week (On-Site) Location ... and manage assigned clinical trials in compliance with GCP, ICH, FDA regulations, and IRB ...
Manhattan, NY · On-site
$150K - $228K/yr
Director of Clinical Research (PT/FT) Deliberate AI Hybrid (NYC or Boston)Full-Time or Part-Time ... You'll manage IRB submissions and regulatory compliance across our multi-site trial portfolio. And ...
Manhattan, NY · On-site
$150K - $228K/yr
Director of Clinical Research (PT/FT) Deliberate AI Hybrid (NYC or Boston)Full-Time or Part-Time ... You'll manage IRB submissions and regulatory compliance across our multi-site trial portfolio. And ...
New York, NY · On-site
$30/hr
RESEARCH MANAGER Location: 1 Washington Square North, NY, NY 10003 PART TIME (5 days/week -30 hours ... IRB Duties * Perform other related activities as required Qualifications Required Education ...
New York, NY · On-site
$30/hr
RESEARCH MANAGER Location: 1 Washington Square North, NY, NY 10003 PART TIME (5 days/week -30 hours ... IRB Duties * Perform other related activities as required Qualifications Required Education ...
Birmingham, AL · On-site
$35K - $49K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting ... Conducts and understands all study activities in accordance with the protocol, IRB regulations, and ...
Birmingham, AL · On-site
$35K - $49K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting ... Conducts and understands all study activities in accordance with the protocol, IRB regulations, and ...
New York, NY · On-site
$30/hr
... and manage quantitative data using REDCap • Contribute to the interpretation and written ... with IRB protocols and human subjects research procedures • Experience supporting academic ...
New York, NY · On-site
$30/hr
... and manage quantitative data using REDCap • Contribute to the interpretation and written ... with IRB protocols and human subjects research procedures • Experience supporting academic ...
This is a full-time or part-time Clinical Research Coordinator position offered through Clinical ... Position-specific responsibilities • Adhere to an IRB approved protocol and submit protocol ...
This is a full-time or part-time Clinical Research Coordinator position offered through Clinical ... Position-specific responsibilities • Adhere to an IRB approved protocol and submit protocol ...
Rancho Mirage, CA · On-site
$22.83 - $34.51/hr
Varies (United States of America) Hours: 24 Salary range: $22.83 - $34.51 Schedule: Part Time Shift ... Board or IRB) in order to obtain its approval for the clinical trials to proceed. Acts as a ...
Rancho Mirage, CA · On-site
$22.83 - $34.51/hr
Varies (United States of America) Hours: 24 Salary range: $22.83 - $34.51 Schedule: Part Time Shift ... Board or IRB) in order to obtain its approval for the clinical trials to proceed. Acts as a ...
Burlington, MA · On-site
$60K - $65K/yr
... IRB submissions, and maintain required trial files and systems. This role is a hybrid, with a ... Manage Good Clinical Practice (GCP) and Human Subjects training for all staff * Manage provider CME ...
Quick apply
Burlington, MA · On-site
$60K - $65K/yr
... IRB submissions, and maintain required trial files and systems. This role is a hybrid, with a ... Manage Good Clinical Practice (GCP) and Human Subjects training for all staff * Manage provider CME ...
$58.5K - $62.2K
6% of jobs
$62.2K - $66K
7% of jobs
$66K - $69.7K
2% of jobs
$69.7K - $73.4K
6% of jobs
$74.5K is the 25th percentile. Wages below this are outliers.
$73.4K - $77.1K
9% of jobs
The median wage is $78.9K / yr.
$77.1K - $80.9K
40% of jobs
$81.5K is the 75th percentile. Wages above this are outliers.
$80.9K - $84.6K
20% of jobs
$84.6K - $88.3K
6% of jobs
$88.3K - $92K
1% of jobs
$92K - $95.8K
0% of jobs
$95.8K - $99.5K
1% of jobs
$58.5K
$78.6K
$99.5K

Part-time
Medical, Dental, Vision, Life, Retirement
Posted 15 days ago
The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This position is primarily on-campus in Baton Rouge.
The IRB Analyst supports protocol review processes, provides regulatory guidance to investigators, and assists in maintaining compliance with federal, state, and institutional requirements governing human subjects research.
Job Responsibilities:
Protocol Pre-Review: Conduct administrative and regulatory pre-reviews of IRB submissions, including new protocols, amendments, continuing reviews, and reportable events, to ensure completeness and compliance. (40%)
Investigator Support: Provide guidance to faculty, staff, and student researchers regarding IRB processes, submission requirements, and applicable regulations. (20%)
Meeting Coordination: Assist in preparing IRB meeting materials, including agendas and protocol assignments, and document proceedings through detailed meeting minutes. (10%)
Reliance Agreements: Support coordination of single IRB (sIRB) reliance agreements for multi-site studies, serving as a liaison between internal and external stakeholders. Data Use Agreements: Assist with processing and tracking data use agreements (DUAs) associated with IRB protocols. (10%)
Regulatory Compliance: Maintain working knowledge of applicable regulations, including the Common Rule (45 CFR 46), HIPAA, and institutional policies. (5%)
Educational Resources: Contribute to the development and maintenance of IRB guidance materials, website content, and training resources to support the research community. (5%)
Quality Assurance: Participate in internal audits and quality improvement activities to ensure ongoing compliance with regulatory and institutional standards. (5%)
Other duties as assigned. (5%)
Minimum Qualifications:
Bachelor's degree in public health, social sciences, biomedical sciences, research administration, or a related field. Basic knowledge of human subjects research protections and applicable regulations (e.g., Common Rule, HIPAA).
Candidates who have relevant experience in key job responsibilities are encouraged to apply-a degree is not required as long as the candidate meets the required years of experience specified in the job description.
Preferred Qualifications:
Bachelor's degree in public health, social sciences, biomedical sciences, research administration, or a related field. Basic knowledge of human subjects research protections and applicable regulations (e.g., Common Rule, HIPAA). Strong written and verbal communication skills. Demonstrated organizational skills and attention to detail. Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft Office and electronic research administration systems. Experience in an IRB office or human subjects protection program. Familiarity with federal, state, and institutional research compliance requirements.Experience supporting IRB operations, including protocol review, meeting documentation, or multi-site research coordination.
Additional Information:
This position is in-person and part-time (20 hours per week).
Background Check - An offer of employment is contingent on a satisfactory pre-employment background check.
Benefits - LSU offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!
Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.
Essential Position (Y/N):LSU is an Equal Opportunity Employer.All candidates must have valid U.S. work authorization at the time of hire and maintain that valid work authorization throughout employment. Changes in laws, regulations, or government policies may impact the university's ability to employ individuals in certain positions.
HCM Contact Information:For questions or concerns related to updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu. For questions or concerns regarding the status of your application or salary ranges, please contact the department using the information provided in the Special Instructions section of this job posting.