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Robin Marcus

Head of Global Decentralized Trials Market Development

Marken

Talk to Robin about these topics and more: 

  • Optimizing and deploying patient-centric DCT services
  • Enhancing investigator site operations and reducing site burden
  • Ensuring high-quality biological sample collection and transport
  • Clinical research options for patient recruitment, adherence and retention
  • Strategies for addressing study challenges and recovering momentum

Clinical Trial Retention

Clinical Trial Supply

Clinical Trial Technology

Clinical Trials

Decentralized Clinical Trials (DCTs)

Diversity

eCOA

eSource

Healthcare

Marketing & Commercialization Strategy

Neurology

Packaging and Labeling

Paperless

Patient Recruitment

Real-World Data

Research and Development

Research as Care

Risk Mitigation

Supply Chain

Vaccines

Women's Health

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Rohin Iyer, Ph.D.

Senior Director Cell and Gene Operations

Marken

Talk to Rohin about these topics and more: 

  • Biomanufacturing & process development for cell & gene therapies 
  • Culture expansion of CAR-T cells, NK cells and mesenchymal stem cells 
  • Cold chain logistics and supply chain considerations for ATMPs 
  • Tissue engineering and regenerative medicine best practices 
  • Bioreactor development and scale-up/out  

Cell and Gene (CGT)

Next Generation Biotherapeutics

Research and Development

Supply Chain

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Brian Fagan

Vice President, Operations

Experic

Talk to Brian about these topics and more: 

  • Clinical supply chain management 
  • Project management 
  • Strengthening customer relationships through consistent delivery 
  • Packaging, labeling, distribution, returns, accountability, and destruction of investigational medicinal products

Clinical Trial Supply

Contract Development Manufacturing Organization (CDMO)

Drug Delivery

Inhalation

Manufacturing Operations

Packaging and Labeling

Quality

Supply Chain

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Christiane Bardroff

Chief Operating Officer

Rentschler Biopharma

Talk to Christiane about these topics and more: 

  • Process development and cGMP manufacturing for clinical and commercial biopharmaceuticals 
  • Navigating international regulatory bodies for global pharmaceutical product releases 
  • Nurturing collaborative relationships with client partners to accelerate speed to clinic and market 
  • Automation and digitalization in biopharmaceutical manufacturing  
  • Trends and predictions in the biopharmaceutical industry 

Automation

Biopharmaceuticals

Contract Development Manufacturing Organization (CDMO)

Engineering

Good Manufacturing Practice (GMP)

Manufacturing Operations

Quality

Regulatory

Supply Chain

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