Regulatory Associate - Cherry Hill

+We are hiring Regulatory Associate for one of our clients. · +Regulatory Affairs Associate to work with our client. · ...

Publishing associate responsible for regulatory submissions to global health authorities. · ...

We are one of the fastest growing IT Consulting company across the USA and we are hiring Regulatory Affairs Specialist for one of our clients. · This position is responsible for assisting with the preparation, coordination and monitoring of routine US regulatory submissions (e.g. ...

Support regulatory activities including preparation and submission of Annual Reports and supplements to FDA for approval. · Reviews and approves labeling for revisions to current products. · Drafts revised labeling (Package Inserts) for marketed products based on FDA requirements ...

The University of Pennsylvania seeks an Associate Director for Regulatory Affairs to oversee clinical research regulatory operations. The successful candidate will have expertise in GCP regulations and experience with IND/IDE/Expanded Access Applications. · Oversight of regulator ...

+Job summaryThis role supports financial services clients by managing operational processes related to regulatory reporting and data accuracy. · +Bachelor's degree in Business, Actuarial Science, Management Information Systems, Risk Management, Human Resources or a related field ...

The University of Pennsylvania seeks an Associate Director for Regulatory Affairs to oversee clinical research regulatory operations within the department/division. · ...

This role will lead regulatory activities for SERB's products developing and implementing preparation of submissions relevant to assigned products and/or projects to FDA. · ...

· Come and Save Lives with Us · SERB is a fast-growing specialty pharmaceutical company that equips healthcare providers worldwide with life-saving medicines for patients facing rare conditions and emergencies. · For over 30 years we have consistently provided emergency medicine ...

· Company Description · Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, ...

· Company Description · Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, ...

The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. This role is responsible for driving regulatory submissions and ensuring compliance with global regulatory requiremen ...

Description · Purpose · The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. This role is responsible for driving regulatory submissions, providing strategic input on cli ...

The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · ...

The Associate Director of Regulatory Affairs - Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · Contribute to the design and execution of global regulatory strategy for Ocugen's gene therapy programs. · Collabor ...

The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · ...

The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · Contribute to the design and execution of global regulatory strategy for Ocugen's gene therapy programs. · Collabor ...

This individual will report into our US Head of Regulatory Affairs and is expected to work out of our US Headquartered office in West Conshohocken on a hybrid schedule with 3 days a week in office. · This individual will be responsible for leading regulatory activities for SERB's ...

We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. · ...

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. · ...