Associate Director Clinical QA

The Associate Director, Clinical Quality Assurance is responsible for vendor quality and compliance risk for vendors participating in GCP, GLP, GPvP, and CSV regulated environments across product modalities. Developing, maintaining, and disseminating vendor data and analytics, including performance indicators, quality metrics, and a vendor risk scorecard....

Contracted Opportunity through the End of 2024 (Potential to be extended)Compensation: $35/hr to $40/hr. Exact compensation may vary based on several factors, including skills, experience, and education.Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA...

Contracted Opportunity through the End of 2024 (Potential to be extended)Compensation: $35/hr to $40/hr. Exact compensation may vary based on several factors, including skills, experience, and education.Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA...

Contracted Opportunity through the End of 2024 (Potential to be extended)Compensation: $35/hr to $40/hr. Exact compensation may vary based on several factors, including skills, experience, and education.Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA...

DescriptionTitle QA Validation Manager Main Purpose The QA Validation Manager/Sr. Manager is responsible for the oversight and implementation of the Marken Quality Management System (QMS), Marken Standard Operating Procedures (SOPs), processes, and policies required to manage validation life cycles, calibration and maintenance of equipment/facilities used...

DescriptionTitle QA Validation Manager Main Purpose The QA Validation Manager/Sr. Manager is responsible for the oversight and implementation of the Marken Quality Management System (QMS), Marken Standard Operating Procedures (SOPs), processes, and policies required to manage validation life cycles, calibration and maintenance of equipment/facilities used in...

Clinical Supply Consulting is currently seeking a Clinical Supply Manager to partner with study teams, vendors, and various internal and external stakeholders to ensure the delivery and execution of a clinical supply plan that supports study protocols and timelines. This is a fully remote role but occasionally, on an as-needed basis, you may be asked to...

Clinical Supply Consulting is currently seeking a Clinical Supply Manager to partner with study teams, vendors, and various internal and external stakeholders to ensure the delivery and execution of a clinical supply plan that supports study protocols and timelines. This is a fully remote role but occasionally, on an as-needed basis, you may be asked to...

The Director/Senior Director, Clinical Pharmacology is a highly scientific strategic role leading multiple facets of Clinical Pharmacology, including study design, PK and PK/PD analyses, and overall drug development support. This individual will be responsible for developing and implementing the clinical pharmacology strategy for Venatorx's product...

Required Skills and Experience:-Bachelor's Degree required in Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsNice to Have Skills and Experience:-Clinical product experience-GMP...

Required Skills and Experience:-Bachelor's Degree required in Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsNice to Have Skills and Experience:-Clinical product experience-GMP...

Required Skills and Experience:-Bachelor's Degree required in Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsNice to Have Skills and Experience:-Clinical product experience-GMP...

Requirements: -Bachelor’s Degree required; focused degree preferred in Engineering, Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsPreferred:-Clinical product experience-GMP Manufacturing...

Requirements: -Bachelor’s Degree required; focused degree preferred in Engineering, Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsPreferred:-Clinical product experience-GMP Manufacturing...

Requirements: -Bachelor’s Degree required; focused degree preferred in Engineering, Science, or equivalent technical subject area-5-7 years of experience working within the pharmaceutical field within QA activities (quality oversight) in GMP manufacturing-Strong experience working with change controlsPreferred:-Clinical product experience-GMP Manufacturing...

Director, Clinical Trials Management/Clinical OperationsFLSA: ExemptReports to: President, R&DLocation: HybridDate Prepared: 21,05,2024The successful candidate will have demonstrated successful experience managing clinical operations in small or mid-sized CROs and/ or biopharmaceutical companies. Experience in the areas of radiopharmaceutical imaging,...

Janssen Research & Development, LLC. is recruiting for an Associate Director, Cell Therapy Laboratory Automation that can be based in Malvern, PA, Cork, Ireland, or Leiden, Netherlands. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and...

Job Details Job Location: Main Corporate Office - Malvern, PA Salary Range: Undisclosed Description Job Purpose The Clinical Research Associate is a key member of Ocugen's clinical trial management team and integral to the successful planning and execution of clinical studies. This individual will develop and maintain strong, productive relationships...

Janssen Biotech, Inc a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Associate II This position will be located in Malvern, PA. At Johnson & Johnson, we believe health is everything Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where...

Job TitleDirector, Clinical Wireless OperationsJob DescriptionDirector, Wireless Operations AM&D Heart (Malvern, PA or Hamilton, NJ)The Director of the Wireless Operations will provide direct and indirect support for our staff at multiple Independent Diagnostic Testing Facilities (IDTF) throughout the United States that provide remote cardiac monitoring...