Sponsor Partnerships

Accelerate your clinical development with our experienced research team and advanced capabilities

Why Partner With Biomed

At Biomed Clinical Research, we understand that effective clinical development requires not just scientific excellence, but operational efficiency and strategic insight. For over 15 years, we've partnered with leading pharmaceutical, biotechnology, and medical device companies to accelerate their path to market.

Our integrated approach combines therapeutic expertise, advanced technology platforms, and a robust network of investigators to deliver high-quality data and timely results. We pride ourselves on flexibility, transparency, and collaborative partnership models that align with your specific development needs.

300+
Successful Trials
95%
On-time Completion
50,000+
Patient Database
15+
Years Experience

Comprehensive Services

End-to-end clinical development solutions tailored to your requirements

Protocol Development & Design

Our medical and scientific experts collaborate with your team to design robust protocols that maximize insights while optimizing resources and timelines.

  • Expert protocol review and optimization

  • Statistical power calculations

  • Endpoint selection guidance

  • Inclusion/exclusion criteria refinement

Patient Recruitment & Retention

Our proven recruitment strategies and dedicated patient engagement team ensure optimal enrollment rates and exceptional retention throughout your study.

  • Targeted recruitment campaigns

  • Community outreach programs

  • Digital recruitment platforms

  • Retention and compliance monitoring

Clinical Operations Management

Comprehensive oversight of all operational aspects of your trial, from site selection and initiation through study close-out.

  • Site identification and qualification

  • Investigator training and support

  • Study monitoring and site management

  • Risk-based quality management

Data Management & Biostatistics

Advanced data capture systems and expert biostatistical analysis to ensure high-quality, reliable results that support your development objectives.

  • EDC system implementation

  • Data validation and query management

  • Interim and final statistical analysis

  • Regulatory-compliant reporting

Regulatory Affairs & Submissions

Expert guidance through the regulatory landscape to facilitate timely approvals and ensure compliance throughout the development process.

  • IND/IDE preparation and submissions

  • Regulatory strategy development

  • Ethics committee/IRB interactions

  • Regulatory compliance monitoring

Medical Writing & Publications

Scientific and regulatory documentation prepared by experienced medical writers to effectively communicate your study findings.

  • Clinical study reports

  • Regulatory documents

  • Publication planning and execution

  • Conference abstracts and presentations

Therapeutic Expertise

Specialized knowledge across key therapeutic areas

Cardiovascular

Heart failure, coronary artery disease, arrhythmias, hypertension, lipid disorders, thrombosis

Neurology

Alzheimer's disease, Parkinson's disease, multiple sclerosis, stroke, epilepsy, pain management

Oncology

Solid tumors, hematological malignancies, immuno-oncology, targeted therapies, biomarker studies

Immunology

Rheumatoid arthritis, psoriasis, inflammatory bowel disease, lupus, transplantation

Metabolic Disorders

Diabetes, obesity, NASH, rare metabolic disorders, endocrine conditions

Infectious Diseases

Viral infections, bacterial infections, vaccines, antimicrobial resistance, tropical diseases

Respiratory

Asthma, COPD, cystic fibrosis, idiopathic pulmonary fibrosis, pulmonary hypertension

Pediatrics

Rare diseases, genetic disorders, pediatric formulations, age-appropriate clinical design

Partner Testimonials

What our sponsors say about working with Biomed Clinical Research

Biomed’s scientific expertise and operational efficiency were instrumental in the successful completion of our Phase III program. Their ability to anticipate challenges and implement effective solutions kept our development timeline on track, ultimately helping us achieve regulatory approval ahead of schedule.
— Dr. Michael Stern - Chief Medical Officer, PharmaTech Innovations
When our initial CRO struggled with patient recruitment for our rare disease study, we transferred the program to Biomed. Their specialized recruitment strategies and site relationships helped us recover lost time and complete enrollment ahead of our revised timeline.
— Jennifer Wong - Director of Clinical Operations, BioGenesis Therapeutics
The transparency and communication we experienced with Biomed set them apart from other research organizations. Their project management team provided consistent updates and involved us in key decisions, making them feel like a true extension of our development team rather than just a service provider.
— Robert Johnson - VP of Clinical Development, MedDevice Solutions

Contact Our Partnership Team