- Merck & Co. (North Wales, PA)
- …in compliance with departmental and company Standard Operating Procedures, regulatory requirements, and standards.- Primary Activities :Business System Ownership ... processes, assuring they are of high quality and complaint with regulatory requirements Skills Education and Minimum Requirement :BA/BS in Computer Science,… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Organon & Co. (Plymouth Meeting, PA)
- …the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate Director) is responsible for ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team… more
- Merck (North Wales, PA)
- **Job Description** **Biomarker Diagnostics Operations, Associate Principal Scientist , Clinical Research** We are currently seeking an Associate ... and diagnostic partners: You will work closely with scientists, regulatory experts, and clinical and biomarker operations teams to...to at every stage + Contribute to filings and regulatory interactions as needed + Work closely with other… more
- Merck (West Point, PA)
- **Job Description** Associate Principal Scientist to support mutagenic and non-mutagenic risk assessment activities as well as perform in silico assessments ... group within the Nonclinical Drug Safety organization is seeking an office-based scientist with expertise in impurity risk assessment. A core responsibility will be… more
- Merck (West Point, PA)
- **Job Description** Our company, a global healthcare leader, is seeking an Associate Principal Scientist to join our collaborative, dynamic, and inclusive ... local regulations and AAALACi standards. Ensure close collaboration with principal investigators in various functional areas, scientific staff, veterinarians,… more
- Merck (North Wales, PA)
- …drugs and vaccines for the benefit of patients and global human health. The Associate Principal Scientist , Clinical Trial Analysis and Reporting leads the ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Merck (West Point, PA)
- …and Clinical Supply Manufacturing. We are seeking an innovative, highly motivated, and experienced Associate Principal Scientist to join us at our research ... small technical development teams + Experience in authoring and reviewing CMC regulatory documentation The successful candidate will be expected to demonstrate the… more
- Merck (West Point, PA)
- …create a healthier future for all. We have an exciting opportunity for an ** Associate ** ** Principal Scientist ** with experience in Vaccine biology or ... professional development. + Properly document protocols and findings, author preclinical regulatory documents, and comply with all laboratory safety requirements. +… more
- Merck (North Wales, PA)
- …in compliance with departmental and company Standard Operating Procedures, regulatory requirements, and standards. **Primary Activities** **:** + Business System ... processes, assuring they are of high quality and complaint with regulatory requirements **Skills** **Education and Minimum Requirement** **:** + BA/BS in… more
- Merck (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Pfizer (Collegeville, PA)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... the clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. + The specific components of safety data… more
- Pfizer (Collegeville, PA)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... the clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. + The specific components of safety data… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist )** has primary responsibility for the strategic planning and directing clinical ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May… more
