- Study Start-Up
- Clinical Trial Management
- Clinical Trial Monitoring
- Investigational Product Solutions
- Data Sciences & Statistical Solutions
- Medical Leadership Services
- Drug Safety & Pharmacovigilance
- Global Regulatory Solutions
- Quality Excellence & Risk Management
- Technology
- Sites & Subjects
- DEI in Clinical Trials
- Decentralized Clinical Trials
Medical Leadership Services
Seamlessly Embedded Medical Expertise for Clinical Trial Success
We recognize the increasing complexity of clinical trials and the critical role of medical expertise in navigating challenges. Our Medical Leadership Services (MLS) model embeds therapeutic leadership throughout the trial lifecycle, delivering strategic insights and actionable guidance from the outset. By seamlessly integrating medical, operational, and regulatory expertise, we provide unparalleled support to ensure your trial’s efficiency and success.
Comprehensive Therapeutic Expertise
iGlobal’s team of globally recognized medical professionals brings specialized knowledge across a wide range of therapeutic areas, including:
- Oncology and Hematology
- Infectious Diseases and Advanced Therapies
- Cardiovascular, Neurology, and Psychiatry
- Metabolic, Endocrine, and Liver Diseases
- Autoimmune Disorders and Nephrology
- Ophthalmology and Rare Diseases/Pediatric Indications
Our expertise extends to crossover and niche areas, offering tailored solutions for even the most complex studies.
Core Medical Leadership Services
Our team provides end-to-end medical leadership and strategic direction across all phases of clinical development, enabling more efficient trials and better subject outcomes. Key services include:
- Integrated Medical Expertise: Embedded leadership that ensures continuous alignment with therapeutic goals and protocol requirements.
- Customized Strategic Direction: Tailored solutions for sponsors of all sizes, from emerging biotechs to global pharmaceutical companies.
- Medical Monitoring Services: Proactive oversight to ensure subject safety and adherence to trial protocols.
- Regulatory Collaboration: Support for interactions with regulatory agencies, working closely with global regulatory affairs teams.
- Study Team Training: Comprehensive protocol and study training for investigators and operational teams.
- Investigator Engagement: Building interactive, productive relationships with investigators to drive trial success.
Integrated Medical, Regulatory, and Operational Excellence
Our global team of medical experts collaborates seamlessly with operational and regulatory teams, providing strategic insights that enhance trial design and execution. This integrated model ensures:
- Collaboration with central labs, bioanalytical laboratories, imaging core labs, and ECG core labs.
- Guidance during protocol development, risk assessments, and regulatory submissions.
- Cross-functional alignment to address challenges proactively and maintain compliance.
Advanced Clinical Practitioners (ACPs): Bridging Science and Operations
iGlobal’s Advanced Clinical Practitioners (ACPs) bring a unique combination of clinical and operational expertise to your study. These highly skilled professionals:
- Evaluate protocols with a focus on subject and site perspectives, ensuring feasibility and operational efficiency.
- Support recruitment strategies, safety event reviews, and team training to enhance trial outcomes.
- Provide ongoing study support by identifying potential challenges early in the planning process and offering practical solutions.
By embedding ACPs in the study team, we streamline execution while prioritizing the subject experience, delivering a smarter, subject-centric approach to clinical trials.
The iGlobal Advantage in Medical Leadership Services
- Embedded Expertise: Seamlessly integrating medical leadership into every phase of your trial for a proactive, strategic approach.
- Comprehensive Support: From regulatory guidance to investigator engagement, our services adapt to meet the unique challenges of each trial.
- Subject-Focused Solutions: Our advanced practitioners and medical monitors ensure trials are designed with subject safety and site practicality in mind.
- Unmatched Collaboration: Cross-functional integration ensures your trial benefits from the combined expertise of medical, operational, and regulatory teams.
Partner with iGlobal Clinical Research for Medical Leadership Services that transform complexity into actionable solutions—ensuring your trial progresses with efficiency, precision, and impact.
