Chief Financial Officer

Capricor Therapeutics Provides Regulatory Update on Deramiocel BLA Following FDA Review of HOPE-3 Topline Data

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Capricor Therapeutics and Parent Project Muscular Dystrophy to Host Webinar Highlighting Positive Phase 3 HOPE-3 Topline Results in Duchenne Muscular Dystrophy

Manager, CMC Regulatory Affairs

Capricor Therapeutics is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. The Manager, CMC Regulatory Affairs is responsible for executing Chemistry, Manufacturing, and Controls (CMC) regulatory activities and ensuring compliance with global regulatory requirements throughout the product lifecycle.

President and CEO

SEQSTER and Praxis expand collaboration to expedite CNS disorder trials

SEQSTER Announces Expanded Partnership with Praxis Precision Medicines to Accelerate Clinical Trials in CNS Disorders

Lipid Nanoparticle Manufacturing Market: An 18.9% CAGR Market Driven by Nucleic Acid Therapies

Praxis Precision Medicines Appoints Global Epilepsy Leader Dr. Orrin Devinsky as Head of Clinical Strategy

Senior Manager/Associate Director, CMC Regulatory Affairs

Praxis Precision Medicines is a clinical-stage biopharmaceutical company focused on developing therapies for central nervous system disorders. The Senior Manager, Regulatory CMC will be responsible for the planning, preparation, and execution of CMC regulatory activities for investigational and commercial products, collaborating with cross-functional teams and external vendors.

Recruiter, Pharma/CRO Staffing Division

Katalyst HealthCares & Life Sciences on LinkedIn: Candidate Portal

CMC Regulatory Affairs Manager

Katalyst CRO is a company focused on regulatory affairs in the pharmaceutical industry, and they are seeking a CMC Regulatory Affairs Manager to lead the preparation and submission of regulatory filings. The role involves providing regulatory guidance, ensuring compliance with regulations, and collaborating with cross-functional teams throughout the product development lifecycle.

Regulatory Affairs Manager

Katalyst CRO is seeking a Regulatory Affairs Manager to support the preparation and submission of CMC sections for regulatory filings. The role involves coordinating with internal stakeholders, maintaining submission plans, and ensuring compliance with evolving regulatory requirements in the biotechnology industry.

Regulatory Affairs Manager � CMC

Chief Executive Officer - General Manager

Senior Human Resources Business Partner / Associate Director Human Resources

Chiesi Announces FDA Acceptance of New Drug Application for its Triple Combination Inhaler for the Maintenance Treatment of Asthma

2025 NCS CME Symposium - Optimizing the Management of Blood Pressure in Acute Cerebrovascular Emergencies

Oak Hill Bio and Chiesi enrol first subject in BPD trial in infants

Cary headquarters plays crucial role in $160 million deal

Sr. Manager, CMC Regulatory Affairs

Chiesi USA, Inc. is an international biopharmaceutical group focused on promoting a healthier world through innovative drug development. They are seeking a Senior Manager in Regulatory Affairs with expertise in CMC to support their Global Rare Diseases portfolio, managing regulatory documents and collaborating with cross-functional teams.

Manager, Cmc Regulatory Affairs

Manager, Cmc Regulatory Affairs in united states (1000+)

Manager, CMC Regulatory Affairs

Senior Manager/Associate Director, CMC Regulatory Affairs

CMC Regulatory Affairs Manager

Regulatory Affairs Manager � CMC

Sr. Manager, CMC Regulatory Affairs