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Michael Rogan

Senior Mobile Experience Director

Greenphire

Talk to Michael about these topics and more: 

  •  Mobile patient experience
  • Patient registries
  • Mental health of clinical trial participants
  • Managing participant travel and reimbursement  

Automation

Behavioral Health

Clinical Strategic Planning

Clinical Trial Payments

Clinical Trial Retention

Clinical Trial Technology

Clinical Trials

Financial Management

Participant Travel

Patient Recruitment

Patient-engagement

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Cyrus Gill

Executive IRB Chair

Univo IRB

Talk to Cy about these topics and more:  

  • Compliance with human research protection regulations and guidelines  
  • IRB member therapeutic and research expertise  
  • Demystifying the IRB review process  

Clinical Data

Clinical Trials

Machine Learning

Preclinical

Programming

Real-World Data

Research and Development

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Julie Blasingim 

CEO

Univo IRB

Talk to Julie about these topics and more:  

  • Human research protection regulations  
  • Site operations of clinical research  
  • Next-generations IRBs  

Clinical Data

Clinical Trials

Machine Learning

Preclinical

Programming

Real-World Data

Research and Development

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Alyssa Greiner

Spokesperson

Clinical Trials For All

Talk to Alyssa about these topics and more:  

  • Dispelling misconceptions about clinical research  
  • Enabling research in underrepresented communities  
  • Bringing health care practices into clinical research  

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Joan Chambers

Senior Consultant, Tufts Center for the Study of Drug Development

Talk to Joan about these topics and more: 

  • Global Investigative Site Landscape
  • Decentralized Clinical Trial Solutions
  • Community Engagement for Clinical Trials
  • Collaborating with Patients and Patient Advocacy Groups for Clinical Trials
  • Clinical Research as a Care Option

CEO

Clinical Trial Retention

Communication Strategies

Diversity

Market Research

Patient Recruitment

Research as Care

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Oren Beske, Ph.D. 

Amalgamator of Business and Biology

ATUM

Talk to Dr. Beske about these topics and more: 

  • Cell line development 
  • Leap-In Transposase and Transposons 

Analytical Testing

Artificial Intelligence (AI)

Bioanalytical Testing

Biologics Manufacturing

Biopharmaceuticals

Cell and Gene (CGT)

CMC

Contract Development Manufacturing Organization (CDMO)

Contract Research Organization (CRO)

Large Molecules

Licensing Strategies

Machine Learning

Phase I/Early Phase Research 

Preclinical

Protein Purification

Quality

Research and Development

Vaccines

Viral Vector Development

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Claes Gustafsson, Ph.D. 

Chief Commercial Officer

ATUM

Talk to Dr. Gustafsson about these topics and more: 

  •  GPS Platform 
  • Protein Engineering 
  • AI Machine Learning 
  • Protein Analytics 

Analytical Testing

Artificial Intelligence (AI)

Bioanalytical Testing

Biologics Manufacturing

Biopharmaceuticals

Cell and Gene (CGT)

CMC

Contract Development Manufacturing Organization (CDMO)

Contract Research Organization (CRO)

Large Molecules

Licensing Strategies

Machine Learning

Phase I/Early Phase Research 

Preclinical

Protein Purification

Quality

Research and Development

Vaccines

Viral Vector Development

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Ella Balasa

Patient Advocate

Balasa Consulting

Talk to Ella about these topics and more: 

  • Understanding the patient journey throughout clinical trial involvement and clinical care
  • Patient engagement strategic planning
  • Disease campaign curation
  • Thought leadership, research summaries, and patient-facing materials for cystic fibrosis and rare disease

Cystic Fibrosis

Healthcare

Patient-engagement

Rare Disease

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Mark Penniston

CEO

Atorus

Talk to Mark about these topics and more: 

  • Clinical trial technology solutions 
  • Clinical analytics 
  • Open-source solutions for clinical data 
  • Using SAS and R in symbiotic ways for clinical trial data 

CEO

Clinical Data

Clinical Trial Technology

Clinical Trials

Programming

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Jay W. Mason, M.D.

Chief Medical Officer

Spaulding Clinical, LLC

Talk to Jay about these topics and more:

  • Understanding cardiac safety requirements, including protocol design 
  • Sponsor support at FDA meetings 
  • Early phase development 
  • Working with data and safety monitoring boards 
  • Cardiac arrhythmias and electrophysiology  

Cardiovascular

Clinical Data

Clinical Trials

Contract Research Organization (CRO)

FDA

M.D.

Phase I/Early Phase Research 

Preclinical

Regulatory

Safety

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