Bio Reliance Corporation

Fast-Track Drugs and Biologics, LLC is a contract research organization (CRO) providing strategic planning, clinical trial and regulatory support services to the pharmaceutical and biotech industries for the development and licensure of vaccines and therapeutics for human diseases.

Fast-Track's mission and commitment to our clients is to identify the critical path of pre-clinical and clinical studies and to implement projects required to quickly move products through the development process.

Fast-Track's critical path planning approach ensures our clients the most expedient pathway through the regulatory process with the shortest timeline to product licensure.

Smart Consulting Group provides technical and regulatory compliance support for biotechnology, medical devices, pharmaceuticals, vaccines, and specialty products, solving complex challenges for both the industry and governments.

We provide advisory and support services in a broad range of categories, including but not limited to:

• FDA Regulatory Compliance
• Quality Systems Design and Implementation
• Forensic Analysis for Data Integrity
• GMP, GLP, and GCP Audits
• Assessments and benchmarking
• Compliance and Quality Risk Assessment
• Regulatory Strategy
• Product/Process Development/Manufacturing
• Laboratory Compliance and Operations Analysis
• Documentation Management Support
• Project Management
• Technology Transfer Strategy and Oversight
• Staffing support for highly specialized talent
• Support services to facilitate organizational change

Smart Consulting Group has expertise in solid dosage forms, parenteral pharmaceuticals, a wide range of biological products, vaccines, recombinant products, monoclonal antibodies, cell therapies, tissue-engineered products, and device-combo products.

DP Clinical, Inc. is a privately held Contract Research Organization (CRO) specializing in neurology/CNS (including spinal cord injury), oncology, ophthalmology, infectious disease/vaccines, and rare disease Phase I-IV clinical programs. DP Clinical provides a full complement of clinical trial services to pharmaceutical, biotech, and medical device companies including trial management, monitoring, data management, biostatistics, regulatory, safety monitoring and reporting, and medical writing. Since 1994, we have worked for clients of all sizes — small to large pharmaceutical and biotech companies, academic research institutions, and government sponsors.

DP Clinical provides integrated trial solutions as well as specific service components based on sponsor need. Our comprehensive services include:
• Project management
• Clinical trial monitoring
• Data management
• Biostatistics
• Pharmacovigilance and safety
• Regulatory affairs
• Quality assurance
• Medical writing

Parexel is focused on the development of innovative new therapies to improve the world’s health. We do this by providing a suite of groundbreaking biopharmaceutical development services that help customers across the globe transform scientific discoveries into new treatments for patients. From clinical trial design to regulatory and consulting services to commercial and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.

NOTE: Parexel does not contact candidates for employment using Google Hangout, AOL instant Messenger or any other chat service. Please visit Jobs.Parexel.com to review our official online application.

WCCT Global, an Altasciences company, is a full-service early phase contract research organization (CRO) for the pharmaceutical, biotechnology and medical device industries. We are specialized regulatory and clinical development professionals who offer an innovative, agile and collaborative approach to every program we deliver.

Our Mission: To offer our clients a simple, integrated, outsourcing solution(s) with a focus on customer service that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an entire program, we are committed to helping our clients reach critical decision making milestones sooner by improving ‘speed and ease’ from lead candidate selection to clinical proof of concept with the goal of getting better drugs to the people who need them, faster. As a partner, we continuously look for ways to build our relationships through communication and range of capabilities, offering scientific guidance and creating an environment that provides value for our clients, respect for our participants, care for our research animals, as well as growth for our employees.

WCCT Global, an Altasciences company, offers U.S. and international sponsors access to an expanded breadth of clinical research offerings. Our emphasis is on overseeing and executing early phase trials in healthy volunteers and special populations. We have extensive experience with Phase 1 clinical trials, including First-in-Human (FIH), SAD/MAD, PK/PD, BA/BE, and devices. Our focus includes Ethnobridging, First-in-Human, Infectious Disease & Vaccines, Ophthalmology and Women’s Health. We are an industry-leader in conducting Asian Ethnic Bridging studies (specifically in Japanese volunteers), at our Phase 1 Unit in Cypress, CA.