Job Title: CRA III - Oncology - UK
Job Type Temporary/Seasonal
Location Uk
Start Date ASAP
Salary Negotiable
Ref No 171719-12510
Date Posted 14th Oct 2013
INC Research employees don't accept ordinary. From therapeutic experts to administrative support staff, each member of our 5,000-strong team continually searches for better. Whether that's better clinical development through our unique Trusted Process®, or better insights from the 100-plus countries in which we operate. It means we deliver success faster, not only for our customers and the patients we serve, but also ourselves.
We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with INC Research's Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research.
As a CRAIII working for INC you will be responsible for completing project activities associated with monitoring functions of Phase I-IV clinical research studies while developing mastery and a thorough understanding of the drug development process, Good Clinical Practices (GCP), and relevant regulations.
We are currently specifically seeking a contractor to join us who has experience monitoring Laeukemia studies.
Core Responsibilities
Key Responsibilities will include:
- Responsible for site management and site staff performance including: monitors all types of clinical trials; participates in all types of site visits; assures compliance with all protocol requirements; assures effective patient identification and recruitment plan is in place; assures timely reporting of Adverse Events (AEs)/Serious Adverse Events (SAEs) and protocol violations; ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials.
- Data Handling, Reporting and Tracking & administrative tasks
- You would also perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines
Skills & Attributes
We are seeking candidates with the following key attributes:
- Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
- Practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
- Thorough understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines
- Experience or education indicates a sound basic knowledge of medical and pharmaceutical terminology
If you have any issues, please e-mail the recruitment team at europejobs@incresearch.com
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