114 regulatory coordinator jobs at 77 companies in Limerick, PA
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Regulatory Program Coordinator
Philadelphia or United States
$50k-$55k/yrOnsiteFull Time
Temple University School of Medicine: Public research university serving students through higher education, professional training, and research in Philadelphia.
3+ YOEBachelor’s degree and 3+ years of research or regulatory compliance experience in a research or clinical setting; knowledge of human subjects regulations, auditing, quality assurance, and strong communication and organizational skills.
Microsoft Word, Microsoft PowerPoint, Microsoft Access
Pennington or Hopewell or New Jersey or Pennsylvania or United States
$95k-$124k/yrOnsiteFull Time
Capital Health: A regional non-profit health system in New Jersey.
2+ YOEBachelor of Science in Nursing required, 2 years regulatory affairs experience, NJ and PA RN credentials, knowledge of DNV/CMS standards, proficiency with Word/Excel/PowerPoint and PolicyStat, strong communication and analytic skills.
PolicyStat, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Novi Surveys, Capital Link
Cooper University Health Care: Academic health system providing tertiary care and medical education.
3+ YOEBachelor's degree required (Master's preferred),3+ years clinical research experience, managing regulatory submissions and documentation, strong communication and coordination skills.
Globus MedicalNYSE: GMED: Innovating musculoskeletal technology to improve patient care.
2+ YOEPrepare and submit FDA regulatory submissions (510(k), IDE, PMA), review labeling and documentation, coordinate with cross-functional teams; 2+ years regulatory affairs experience in medical device industry; bachelor’s degree or equivalent.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams
Cooper University Health Care: Academic health system providing tertiary care and medical education.
3+ YOERequires 3–5 years of related experience and a high school diploma; bachelor's degree in biology, research, public health, business, or healthcare administration preferred.
OtsukaTokyo Stock Exchange: 4578: Global healthcare focused on pharmaceuticals, nutraceuticals, and medical devices.
7+ YOEMinimum 7 years regulatory operations experience with eCTD submissions, knowledge of FDA/EMA/Swiss Medic guidance, Documentum and publishing tools, Microsoft Office/SharePoint proficiency, staff supervision and vendor coordination.
Documentum, DocuBridge, InSight Publisher, GlobalSubmit Validate, GlobalSubmit Review, ISIToolbox, eCTD, Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint, Microsoft SharePoint
MSDNYSE: MRK: We use leading-edge science to save and improve lives.
5+ YOEBS or equivalent scientific, technical, or regulatory degree; 5+ years in pharmaceutical or biotech Regulatory CMC; hands-on digital, automation, and AI/LLM experience; change management, mentoring, collaboration, and project coordination skills.
Artificial Intelligence (AI), machine learning, generative AI, AI/LLM, Electronic Common Technical Document (eCTD), Veeva, ERA App
Parkhouse Nursing & Rehabilitation Center: For-profit skilled nursing and rehabilitation center serving older adults in Royersford with short-term rehabilitation, long-term care, and memory care.
Organized, detail-oriented individual to coordinate schedules, monitor staffing levels, maintain records, provide customer service, and ensure regulatory compliance.
Burlington Township or Westampton or Southampton Township or Marlton or Mount Laurel or Willingboro or Trenton or Columbus or Hamilton Township or Camden or Wrightstown or Fort Dix or McGuire Air Force Base or Mount Holly
OnsiteFull Time
OTC Services: Nonprofit vocational rehabilitation provider helping adults with disabilities through employment, day, residential, recycling, and business services.
2+ YOEAssociate degree required; bachelor's preferred. Requires 2–3 years of administrative, compliance, healthcare, regulatory, legal, audit, or project-coordination experience and strong organization, writing, confidentiality, and reporting skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Teams, Relias, PolicyPro, Microsoft SharePoint, learning-management system, compliance systems
Seasons Hospice & Palliative Care: Provider of post-acute home health, hospice, and personal care.
1+ YOE1+ year of hospice experience, strong written and verbal communication, organization, customer service, problem-solving, regulatory familiarity, and stakeholder coordination skills; associate degree preferred.
Acadia PharmaceuticalsThe Nasdaq Stock Market LLC: ACAD: Public biopharmaceutical developing and commercializing medicines for underserved neurological and rare disease patients.
8+ YOEBachelor’s degree in life science; 8+ years regulatory drug development; global submissions experience; willing to travel.
Perelman School of Medicine: Ivy League private research university.
1+ YOEBachelor of Science and 1+ years experience, coordinate clinical trials, IRB submissions, data entry in EDC, safety reporting, biospecimen handling, and regulatory compliance.
PennCTMS, PennChart, Electronic Data Capture (EDC)
Perelman School of Medicine: Ivy League private research university.
2+ YOEBachelor of Science and 2–3 years of experience, or equivalent education and experience; clinical research coordination, data management, regulatory documentation, and participant study support.
Boscov's: Family-owned department store chain based in the United States.
2+ YOERequires 2–3 years in safety-related work with HR support, supervisory or leadership experience, OSHA/EPA regulatory knowledge, Spanish fluency, and strong communication, analytical, and problem-solving skills.
Cambridge Rehabilitation & Healthcare Center: For-profit skilled nursing facility providing post-acute rehabilitation, long-term care, and memory care for older adults.
3+ YOEAccredited nursing program graduate with active New Jersey RN license, 3+ years of long-term care clinical experience, prior MDS/RAI experience, strong assessment skills, and Medicare/Medicaid regulatory knowledge.
DM Clinical Research: Runs a network of clinical trial investigator sites.
2+ YOEHigh school diploma or equivalent required; bachelor's preferred. Requires 2+ years as a clinical research coordinator, English proficiency, and protocol, regulatory, documentation, and patient consent skills.
Electronic Data Capture (EDC), Interactive Voice Response System (IVRS)
Thomas Jefferson University: Private nonprofit research university educating undergraduate, graduate and professional students while advancing health, design, science and medicine.
1+ YOEMinimum clinical research experience (options: HS +6 yrs, BA/BS +2 yrs, MS +1 yr). Knowledge of GCP, IRB/regulatory documentation, patient consent, specimen handling, data management, and trial coordination.