WELCOME TO CLINICAL PROFESSIONALS NETWORK
As a Permanent Placement/Direct Hire Staffing Organization, we are dedicated to serving qualified and committed Clinical Professionals respectfully and in timely fashion. With nearly 20 years of Industry recruiting experience, Clinical Professionals Network serves many areas of the Drug Development lifecycle.
Clinical trials require operational management and thus require key individuals to coordinate the project or particular phase of the drug development process. ... Clinical operations is a highly important part of the drug development process and encompasses the whole clinical trial process from phases I-IV.
Technical operations team design, control, and manage the technical process and operational integrity of technological services provided by an organization. ... Develop and apply firmware, software, and hardware solutions to meet the technical requirements of a company.
Ensuring that pharmaceutical products are manufactured to a safe and consistent standard. QA is a very broad field that refers to any aspect that may affect a drug's quality during its research, development, manufacturing, and sales phases
Taking a data-driven approach to managing a medicine's life cycle, focusing on marketing and selling novel treatments for various disease areas. Members of this group educate healthcare providers, patients and other stakeholders about the science behind the medicine.
The research and development (R&D) process is a critical stage in drug development in the Pharma industry. The process starts after an initial candidate drug is identified and encompasses the rigorous research tests that determine its therapeutic suitability.
Provide scientific and clinical support for commercial products and in effect act as the medical face of the company
To provide our clients with Top Industry Talent, which in turn helps them to achieve their goals of providing patients the needed medication on a timely basis
Regional Clinical Research Associate - West Coast - 2+ years of onsite monitoring with Oncology studies. Click Here to apply.
Drug Safety Associate - Philadelphia, PA - 5+ Years experience in handling Adverse Events, Reporting and Argus database collection. Click Here to Apply
Regulatory Affairs Associate - New York City - 3-5 years Regulatory submissions experience with BLA, NDA and MAA background. Click Here to Apply
Medical Director - Home Based - Adult Oncologists - Serves as department and trial expertise /specialist. Click here to Apply