If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). • Training & Knowledge ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). • Training & Knowledge ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). • Training & Knowledge ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). • Training & Knowledge ...
Author and revise batch records, SOPs, and technical reports;protocols,manufacturing summary reports,ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Author and revise batch records, SOPs, and technical reports;protocols,manufacturing summary reports,ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Vice President, Regulatory Affairs *PC 884
Gaithersburg, MD · On-site
$162K - $213K/yr
ATMP experience is a plus. * Ability to analyze and interpret scientific and technical information, as well as regulatory documents. * Stays abreast of current and evolving regulatory requirements ...
Vice President, Regulatory Affairs *PC 884
Gaithersburg, MD · On-site
$162K - $213K/yr
ATMP experience is a plus. * Ability to analyze and interpret scientific and technical information, as well as regulatory documents. * Stays abreast of current and evolving regulatory requirements ...
Coordinate daily with WFFC/ATMP simulator maintenance teams to track system status and service requests. * Work with course managers to allocate simulation time for formal training. * Coordinate with ...
Coordinate daily with WFFC/ATMP simulator maintenance teams to track system status and service requests. * Work with course managers to allocate simulation time for formal training. * Coordinate with ...
Direct experience with cell therapy, ATMP, or biologics manufacturing automation. * Experience integrating control systems with MES, LIMS, ERP (e.g., SAP), WMS, and clinical systems. * Familiarity ...
Direct experience with cell therapy, ATMP, or biologics manufacturing automation. * Experience integrating control systems with MES, LIMS, ERP (e.g., SAP), WMS, and clinical systems. * Familiarity ...
Principal Process Engineer, Manufacturing Sciences & Technology, Cell Therapy
Los Angeles, CA · On-site
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Principal Process Engineer, Manufacturing Sciences & Technology, Cell Therapy
Los Angeles, CA · On-site
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). Training ...
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). Training ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). Training & Knowledge ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). Training & Knowledge ...
LUH- 72A Lakota Simulator Instructor Operator
Marana, AZ · On-site
$24.25 - $30.50/hr
Coordinate daily with WFFC/ATMP simulator maintenance teams to track system status and service requests. * Work with course managers to allocate simulation time for formal training. * Coordinate with ...
LUH- 72A Lakota Simulator Instructor Operator
Marana, AZ · On-site
$24.25 - $30.50/hr
Coordinate daily with WFFC/ATMP simulator maintenance teams to track system status and service requests. * Work with course managers to allocate simulation time for formal training. * Coordinate with ...
Director, Regulatory Affairs
Blue Bell, PA · On-site
$143K - $189K/yr
DCT, COVID-19, GMO, ATMP development, Cell and Gene therapy etc. * Provide clients with strategic advice in response to their queries, based on regulatory experience and area of expertise, consulting ...
Director, Regulatory Affairs
Blue Bell, PA · On-site
$143K - $189K/yr
DCT, COVID-19, GMO, ATMP development, Cell and Gene therapy etc. * Provide clients with strategic advice in response to their queries, based on regulatory experience and area of expertise, consulting ...
Laboratory Operational Technology and Applications Engineer
East Hanover, NJ · On-site
$107K - $160K/yr
... ATMP) including 21 CFR Part 11. * Project management experience; may include leading teams or projects with demonstrated leadership skills in team building and accomplishing complex projects. * Must ...
Laboratory Operational Technology and Applications Engineer
East Hanover, NJ · On-site
$107K - $160K/yr
... ATMP) including 21 CFR Part 11. * Project management experience; may include leading teams or projects with demonstrated leadership skills in team building and accomplishing complex projects. * Must ...
Experience with stem cell or iPSC-based therapies or other ATMP modalities * Experience supporting or participating in FDA inspections * Experience working with global health authorities, such as EMA ...
Experience with stem cell or iPSC-based therapies or other ATMP modalities * Experience supporting or participating in FDA inspections * Experience working with global health authorities, such as EMA ...
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+) Training & Knowledge ...
Process Engineer
Rockville, MD · On-site
Author and revise batch records, SOPs, and technical reports; protocols, summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+) Training & Knowledge ...
Strong knowledge of GMP regulations and guidance, including 21 CFR Parts 210/211, 600series (biologics), applicable EU GMPs, and ICH guidelines; cell therapy, ATMP, or aseptic processing experience ...
Strong knowledge of GMP regulations and guidance, including 21 CFR Parts 210/211, 600series (biologics), applicable EU GMPs, and ICH guidelines; cell therapy, ATMP, or aseptic processing experience ...
Atmp information
See salary details
$8.89 - $13.70
16% of jobs
$15.17 is the 25th percentile. Wages below this are outliers.
$13.70 - $18.51
29% of jobs
The median wage is $19.71 / hr.
$18.51 - $23.32
19% of jobs
$27.58 is the 75th percentile. Wages above this are outliers.
$23.32 - $28.13
12% of jobs
$28.13 - $32.93
8% of jobs
$32.93 - $37.74
5% of jobs
$37.74 - $42.55
4% of jobs
$42.55 - $47.36
2% of jobs
$47.36 - $52.16
2% of jobs
$52.16 - $56.97
1% of jobs
$56.97 - $61.78
1% of jobs
$8
$26
$61
How much do atmp jobs pay per hour?
What are some common challenges faced by ATM (Automated Teller Machine) Technicians and how can they overcome them?
What are the key skills and qualifications needed to thrive as an Advanced Therapy Medicinal Products (ATMP) Specialist, and why are they important?
What are ATMPs?

Other
Medical, PTO
Posted 17 days ago
Medpace rating
8.4
Based on 8 frontline employees who took The Breakroom Quiz
15th of 57 rated research
Job description
Experienced Clinical Research Associates- accelerate your hematology/oncology career by joining Medpace today!
Home Based Roles with Excellent Compensation & Benefits
including Equity/Stock Option Program and Additional Bonus Programs available
__________________________________
Medpace is an innovative, scientifically oriented mid-sized global CRO that is focused on full-service project work. Our mission is to accelerate the global development of safe and effective medical therapeutics. We are rapidly growing and are seeking experienced Clinical Research Associates to join our team!
We offer a Certificate Program (advanced training curricula) in Hematology/Oncology Monitoring. This program includes a general cancer overview, common indications, treatment options, diagnostic and reference criteria. If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP), and COVID-19.
Applicants with experience in any of the below indications will be considered. Relevant experience includes monitoring as a CRA or working as a study coordinator or clinician.
- Solid Tumor
- Breast/Ovarian/Prostate/Colorectal/Bladder/Lung/Kidney/Pancreatic Cancer
- Small Cell Lung Cancer
- Graft vs Host Disease
- Glioblastoma
- Melanoma
- Leukemia
- Lymphoma
- Mesothelioma
Candidates must have at minimum a Bachelor's degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills.
Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive PTO packages - starting at 20+ days
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
- Discounts for local businesses
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992