Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA) * Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans * Work in ...
Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA) * Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans * Work in ...
Regulatory CMC Director (Cell & Gene Therapy)
Gaithersburg, MD · Hybrid
$162K - $213K/yr
Partner with stakeholders to deliver CMC components of IND, IMPD, BLA, Master Files, amendments, and annual reports; develop health authority briefing documents; represent CMC regulatory affairs on ...
Regulatory CMC Director (Cell & Gene Therapy)
Gaithersburg, MD · Hybrid
$162K - $213K/yr
Partner with stakeholders to deliver CMC components of IND, IMPD, BLA, Master Files, amendments, and annual reports; develop health authority briefing documents; represent CMC regulatory affairs on ...
Regulatory CMC Director (Cell & Gene Therapy)
Gaithersburg, MD · On-site
$162K - $213K/yr
Partner with stakeholders to deliver CMC components of IND, IMPD, BLA, Master Files, amendments, and annual reports; develop health authority briefing documents; represent CMC regulatory affairs on ...
Regulatory CMC Director (Cell & Gene Therapy)
Gaithersburg, MD · On-site
$162K - $213K/yr
Partner with stakeholders to deliver CMC components of IND, IMPD, BLA, Master Files, amendments, and annual reports; develop health authority briefing documents; represent CMC regulatory affairs on ...
Regulatory CMC Director (Cell & Gene Therapy)
Gaithersburg, MD · Hybrid
$186K - $279K/yr
Partner with stakeholders to deliver CMC components of IND, IMPD, BLA, Master Files, amendments, and annual reports; develop health authority briefing documents; represent CMC regulatory affairs on ...
Regulatory CMC Director (Cell & Gene Therapy)
Gaithersburg, MD · Hybrid
$186K - $279K/yr
Partner with stakeholders to deliver CMC components of IND, IMPD, BLA, Master Files, amendments, and annual reports; develop health authority briefing documents; represent CMC regulatory affairs on ...
Scientist II - HSV-1 Viral Vector Process Development
San Diego, CA · On-site
$115K - $150K/yr
Executing process characterisation studies to support regulatory filings (IND/IMPD). * Maintaining detailed laboratory notebooks, confidently presenting data in group meetings and contributing to ...
Scientist II - HSV-1 Viral Vector Process Development
San Diego, CA · On-site
$115K - $150K/yr
Executing process characterisation studies to support regulatory filings (IND/IMPD). * Maintaining detailed laboratory notebooks, confidently presenting data in group meetings and contributing to ...
Experience supporting IP, IND, BLA, MAA, or IMPD submissions. * Demonstrated experience leading programs in an IPD, alliance management, or co-development model; CRDMO/sponsor partnership experience ...
Quick apply
Experience supporting IP, IND, BLA, MAA, or IMPD submissions. * Demonstrated experience leading programs in an IPD, alliance management, or co-development model; CRDMO/sponsor partnership experience ...
Associate Director, Clinical Pharmacology
$185K - $215K/yr
Contribute to the preparation of the IND, IB and IMPD documents * Be able to conduct noncompartmental PK analysis based on preliminary data using standard industry data analysis software * Contribute ...
Associate Director, Clinical Pharmacology
$185K - $215K/yr
Contribute to the preparation of the IND, IB and IMPD documents * Be able to conduct noncompartmental PK analysis based on preliminary data using standard industry data analysis software * Contribute ...
Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA) * Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans * Work in ...
Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA) * Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans * Work in ...
Provide hands-on support in the generation of CMC documents (e.g., Module 2 and Module 3 of eCTD, IMPD, etc.). Qualifications * BA/BS, MS, or Ph.D. in a relevant technical discipline or equivalent ...
Provide hands-on support in the generation of CMC documents (e.g., Module 2 and Module 3 of eCTD, IMPD, etc.). Qualifications * BA/BS, MS, or Ph.D. in a relevant technical discipline or equivalent ...
Senior Director/ Director, CMC Regulatory Affairs
South San Francisco, CA · On-site
$250K - $300K/yr
Provide hands-on support in the generation of CMC documents (e.g., Module 2 and Module 3 of eCTD, IMPD, etc.). Qualifications * BA/BS, MS, or Ph.D. in a relevant technical discipline or equivalent ...
Senior Director/ Director, CMC Regulatory Affairs
South San Francisco, CA · On-site
$250K - $300K/yr
Provide hands-on support in the generation of CMC documents (e.g., Module 2 and Module 3 of eCTD, IMPD, etc.). Qualifications * BA/BS, MS, or Ph.D. in a relevant technical discipline or equivalent ...
Review CMC sections of regulatory submissions (IND, IMPD, BLA etc) for compliance with regulatory requirements and alignment with company strategies. * RA support in interactions with Health ...
Review CMC sections of regulatory submissions (IND, IMPD, BLA etc) for compliance with regulatory requirements and alignment with company strategies. * RA support in interactions with Health ...
Author, review, and approve analytical documentation, including protocols, methods, reports, and regulatory sections (IND/IMPD). * Train QC personnel in analytical techniques, data interpretation ...
New
Author, review, and approve analytical documentation, including protocols, methods, reports, and regulatory sections (IND/IMPD). * Train QC personnel in analytical techniques, data interpretation ...
New
Department of Public Safety-IMPD Opening Date: 02/16/2026 Overview Lateral Police Officer candidates are experienced full-time police officers currently employed by other municipal, county, or state ...
Department of Public Safety-IMPD Opening Date: 02/16/2026 Overview Lateral Police Officer candidates are experienced full-time police officers currently employed by other municipal, county, or state ...
Author, review, and update CMC specific documents to support worldwide regulatory submissions (i.e., IND, IMPD, and NDA) Required Qualifications: * 5+ years of experience in solid-oral dosage form ...
Author, review, and update CMC specific documents to support worldwide regulatory submissions (i.e., IND, IMPD, and NDA) Required Qualifications: * 5+ years of experience in solid-oral dosage form ...
Design and author validation protocols, reports, and method lifecycle documentation for regulatory submissions (IND/IMPD). * Support release and stability testing strategies, including specification ...
Quick apply
Design and author validation protocols, reports, and method lifecycle documentation for regulatory submissions (IND/IMPD). * Support release and stability testing strategies, including specification ...
Director, Regulatory Affairs CMC
$238K - $281K/yr
Provide Regulatory CMC guidance to internal teams and lead cross-functional teams to plan and prepare briefing packages, and CMC sections for INDs, and equivalent IMPD sections for CTAs, NDAs/MAAs ...
Director, Regulatory Affairs CMC
$238K - $281K/yr
Provide Regulatory CMC guidance to internal teams and lead cross-functional teams to plan and prepare briefing packages, and CMC sections for INDs, and equivalent IMPD sections for CTAs, NDAs/MAAs ...
... IMPD, and NDA. * Develop, implement, and improve key clinical supply business processes and SOPs and conduct necessary training. Required Skills, Experience, and Education: * B.Sc. or M.Sc. in a ...
... IMPD, and NDA. * Develop, implement, and improve key clinical supply business processes and SOPs and conduct necessary training. Required Skills, Experience, and Education: * B.Sc. or M.Sc. in a ...
Represent regulatory affairs at study teams; provide guidance and develop strategies to ensure timely submission and approval of study related documents including protocol, IB, DSUR, amendment, IMPD ...
Quick apply
Represent regulatory affairs at study teams; provide guidance and develop strategies to ensure timely submission and approval of study related documents including protocol, IB, DSUR, amendment, IMPD ...
Work experience and knowledge of global regulatory submissions (IND, IMPD, NDA and MAA, etc.) is preferred. * Chromatographic experience in development, optimization, and troubleshooting. #LI-Hybrid ...
Work experience and knowledge of global regulatory submissions (IND, IMPD, NDA and MAA, etc.) is preferred. * Chromatographic experience in development, optimization, and troubleshooting. #LI-Hybrid ...
Executive Director, Global GCP QA
$275K - $325K/yr
EvaluateclinicaltrialIND/IMPD/NDAenablingdocumentation,studyprocesses,andoperational planstoconfirmalignmentwithrelevantglobalregulationsandguidelines.
Executive Director, Global GCP QA
$275K - $325K/yr
EvaluateclinicaltrialIND/IMPD/NDAenablingdocumentation,studyprocesses,andoperational planstoconfirmalignmentwithrelevantglobalregulationsandguidelines.
Impd information
See salary details
$5.1K is the 25th percentile. Wages below this are outliers.
$4.3K - $6.7K
73% of jobs
$7K is the 75th percentile. Wages above this are outliers.
$6.7K - $9.2K
14% of jobs
$9.2K - $11.6K
0% of jobs
$11.6K - $14.1K
0% of jobs
$14.1K - $16.5K
0% of jobs
$16.5K - $19K
0% of jobs
$19K - $21.4K
0% of jobs
$21.4K - $23.9K
0% of jobs
$23.9K - $26.3K
0% of jobs
$26.3K - $28.8K
6% of jobs
$28.8K - $31.3K
6% of jobs
$4.3K
$10K
$31.3K
How much do impd jobs pay per month?
What are the key skills and qualifications needed to thrive as an IMPD (Indianapolis Metropolitan Police Department) officer, and why are they important?
What is the difference between Impd vs Data Analyst?
| Aspect | Impd | Data Analyst |
|---|---|---|
| Required Credentials | Typically requires a degree in engineering, manufacturing, or related fields; certifications like Six Sigma or Lean are common | Requires a degree in statistics, mathematics, or computer science; certifications like CAP or Microsoft Data Analyst are beneficial |
| Work Environment | Primarily in manufacturing or industrial settings, focusing on process improvement and quality control | Mostly in office settings, analyzing data, creating reports, and supporting decision-making |
| Employer & Industry Usage | Used in manufacturing, production, and industrial sectors for process optimization | Used across various industries including finance, healthcare, marketing, and technology for data analysis |
While Impd professionals focus on process improvement within manufacturing environments, Data Analysts interpret data to support business decisions across multiple industries. Both roles require analytical skills but differ in their specific applications and work settings.
What are IMPD officers?
What are some common challenges faced by IMPD officers during their daily patrols?

Job description
Responsibilities
- Contribute to our cutting-edge radiopharmaceutical development program
- Conceptualize, plan, design, place, execute, and summarize clinical trials
- Drive daily vendor and site management, including collaboration with Study Medical Monitor and KOLs to determine the medical and scientific needs
- Effectively communicate project-related information including the planning and execution of meetings and presentations as well as creation and maintenance of metrics, e.g., dashboards, timelines, resources, and budgets
- Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA)
- Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans
- Work in an office (Wilmette, IL north of Chicago) with a dynamic, talented team
Qualifications
MINIMUM EXPERIENCE
- Biotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager
- 7+ years’ experience managing clinical trials including study design and initiation, oversight, study closeout, project management, and regulatory filings
- Demonstrated ability to plan and execute Pharma-Sponsored clinical trials, managing vendors and resources in effective & creative manners to achieve business needs including on-time, on-budget, and on-spec study results for successful use in regulatory marketing applications
- Thorough knowledge of ICH-GCP, Food and Drug Administration (FDA), and European regulations
- Excellent communication (oral and/or written), leadership, and risk mitigation skills plus a positive attitude
- Require minimal guidance; is able to function in an independent manner
- Proven ability to effectively manage internal and external personnel in clinical trial conduct
PREFERRED EXPERIENCE
- 9 years’ clinical trials experience in pharmaceutical or biotechnology firms
- Experience in oncology trials
- Experience managing clinical trials in Europe and/or Australia
- Experience in a small or growth-stage biopharma company
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008