Documentations Coordinator BC Cancer Agency, Research Centre

April 3, 2009BC Cancer Agency, Research Centre
The BC Cancer Agency (BCCA) is committed to reducing the incidence of cancer, reducing the mortality from cancer, and improving the quality of life of those living with cancer. It provides a comprehensive cancer control program for the people of British Columbia by working with community partners to deliver a range of cancer services, including prevention, early detection, diagnosis and treatment, research, education, supportive care, rehabilitation and palliative care. It operates five regional cancer centres in Surrey, Kelowna, Vancouver, Vancouver Island, and Abbotsford, with a sixth centre scheduled to open in Prince George in 2012. The BC Cancer Agency's Research Centre conducts research into the causes and cures for cancer.
BCCA is an agency of the Provincial Health Services Authority (PHSA) which plans, manages and evaluates specialty and province-wide health care services across BC. PHSA embodies values that reflect a commitment to excellence. These include: Patients first • Best value • Results matter • Improvements through knowledge • Open to possibilities.
Regular Part-time position .33 fte
Mon-Wed (shift may change due to operational needs)
0830-1230 hours
Vancouver, BC
As a self-starter with strong administrative and control skills, you will support the Investigational Drug Program (IDP) and department’s laboratory by developing, writing and ensuring compliance with Standard Operating Procedure. Operating in a dynamic environment of deadlines, you will perform quality assurance and quality control processes, including arranging equipment validation and certification, managing regulatory affairs activities, and coordinating and conducting audits. As well, you will manage the IDP document archive system and document training materials, batch record documentations and SOPs. Your effective communication skills enable you to support the IDP laboratory and shipping functions as required. This is a regular part-time position with shifts Mon-Wed, from 0830-1230. Shifts may change due to operational needs.
Possessing a Bachelor of Science degree, you have at least two years’ recent related experience in a research or laboratory environment. You also have experience with drug development processes, quality management systems, writing standard operating procedures and data/documentation management. Your experience includes familiarity with GMP and GLP regulations of the Canadian Health Protection Branch and the US Food and Drug Administration. An equivalent combination of education, training and experience will be considered. Safety focused, you have in-depth knowledge of the WHMIS guidelines and Occupational Health and Safety standards.
For more information about the Agency that you are interested in, please visit the website at www.bccancer.ca
How To Apply:
We invite you to apply by sending your curriculum vitae to Ms. Heidi Cheung at hcheung@bccrc.ca Please reference "Documentation Coordinator" in your application.
Applications will be accepted until this position has been filled.