Linnea Olsson

About Linnea Olsson

I am a dynamic clinical operations leader with over 25 years of experience navigating global clinical trials in the biotechnology sector. My focus is on crafting and implementing clinical operational strategies that not only meet regulatory standards but also align seamlessly with corporate goals. I excel in fostering collaboration among cross-functional teams, sponsors, and CROs, driving project success through exceptional communication and innovative problem-solving. My commitment to operational excellence is evident in my ability to enhance data quality and streamline trial logistics, ensuring compliance with ICH/GCP, FDA, EMEA, and NHS regulations. Through mentorship and training, I am dedicated to nurturing the next generation of leaders in clinical research, paving the way for future advancements in the field.My core expertise spans strategic planning, clinical trial management, and vendor oversight, underpinned by a profound understanding of drug development and patient safety. I lead with a vision, integrating risk management and proactive adjustments into every aspect of clinical operations, from protocol development to study execution. By fostering strong relationships with key stakeholders and driving initiatives like diversity and decentralized clinical trials, I elevate organizational goals while cultivating an environment of innovation and collaboration. I am passionate about transforming the landscape of clinical research, ensuring that we not only meet but exceed the expectations of the patients and communities we serve.Expertise: Strategic Planning & Execution | Clinical Strategy | Clinical Quality | Healthcare Management | Clinical Trial Management | CRO Management | Clinical Development | Clinical Research | Clinical Trials | Drug Development | Investigational New Drug Applications | Patient Safety | People Management | Finance Management | Performance Management | Clinical Data Management

Experience

1. Senior Director of Clinical Operations

   Carrick Therapeutics

   May 2025 — Present · US

Education

• Slippery Rock University

  B.S., Allied Health Sciences

• University of South Florida

  MPH, Masters of Public Health

Skills

• Inform
• Edc
• Therapeutic Areas
• Ctms
• Protocol Implementation
• Regulatory Affairs
• Crf Design
• Clinical Trials
• CRO Management
• Good Clinical Practice (Gcp)
• Medical Writing
• Clinical Data Management
• Oracle Clinical
• Regulatory Requirements
• Ind
• Regulatory Submissions
• Oncology
• Protocol
• Clinical Research
• Neurology
• Infectious Diseases
• Clinical Development
• Trial Management
• Diabetes
• Clinical Monitoring
• Clinical Trial Management System (Ctms)
• Rheumatology
• Clinical Study Design
• Phase I
• Pharmacovigilance
• Clinical Operations
• Clinical Site Monitoring
• Ich-Gcp
• Patient Recruitment
• Site Initiation
• Protocol Designing
• Oncology Clinical Research
• Vaccines
• Endocrinology
• Pharmaceutical Industry