|
Pharmaceutical companies
face significant challenges meeting the needs
that arise during the drug development lifecycle.
These challenges can be even more daunting and
limit the effectiveness of clinical trials without
the correct staff. With resource specialization
in all aspects of drug development, Delta can
assist in the success of your clinical trials
by handling your contract and permanent staffing
needs.
Delta’s clinical research practice concentrates
on ensuring the integrity of the clinical trial
and safety of study participants through placement
of resources including Study Managers, Research
Monitors, Research Coordinators, Research Managers
and Safety Nurses.
Over the last decade it became evident you need
more than basic knowledge of clinical trials databases
to ensure data integrity and the successful management
of your study data. Delta provides experts in
the field including Data Managers, Data Analysts,
Data Support Specialists, SAS Programmers, Biostatisticians
and Bioinformatists.
With the additional emphasis placed on time-to-market
and reduction in the drug development life cycle,
clinical support becomes even more crucial to
the success of your study and ultimately the ability
to commercialize your product. Delta recruits
critical talent such as Medical Writers, Regulatory
Auditors and Quality Assurance Analysts.
Clinical application development is becoming increasingly
complex and requires more than just generic technology
resources. Delta provides a depth of pharmaceutical
systems knowledge and complete application development
programs that meet regulatory requirements and
streamline the drug development process. Some
of the resources we can provide within our Clinical
Development Practice include SAS Developers, Documentum
Developers, Oracle Clinical Developers and Project
Managers/Analysts, to name a few.
|
