Validant has an in-depth knowledge of the Medical Device, Pharmaceutical and Biologics sector and an extensive network of senior level professionals with the niche skill sets that are in high demand in the industry. We combine this market knowledge with our proven technical search capabilities to deliver a comprehensive, high quality search solution for our clients.
Validant helps companies comply with the vast and ever-changing regulatory standards. We help clients efficiently move products past clinical trials, through approvals and into the marketplace. Below is a summary of some of our key areas of focus within Regulatory and Clinical disciplines:
Validant’s has extensive experience in all aspects clinical operations through all phases of clinical drug development from study planning to close out. Our network and capabilities includes the recruitment, consulting for the following:
Validant has a unique combination of FDA, biologic, drug and medical device industry experience for all aspects of Regulatory Affairs. This includes:
Clinical Drug Development / Medical Affairs
Validant has a strong history of recruitment and consulting in Clinical Drug Development and Medical Affairs. We have successfully recruited and placed processionals and consultants for the following roles:
- Medical Science Liaisons
- Medical Directors – Chief Medical Officers
- Medical Writers
- Medical Information
We have a strong track record across multiple therapeutic areas including Oncology, Cardiovascular, Metabolic Disorders, Immunology, Ophthalmology, Infectious Disease, Dermatology and Neurology.
Validant has proven track record in providing Drug Safety staff and consulting services in the following areas:
Clinical Data Management
Validant has extensive experience in consulting, full time placement in Clinical Data Management.
Validant provides Biostatistics and Statistical Programming support for all phases of pre-clinical, clinical stage drug development, and post marketing.