Newly added to DMX's web site today, key positions for expansion, regulatory approval management and production quality control...
Dimethaid is an emerging growth pharmaceutical company that is always looking for strong people to join its team. If you have experience in this exciting industry in the areas of clinical development, regulatory affairs, Quality Assurance/Quality Control, sales or marketing, please send us your resume to the attention of Cindy Carter, Director of Operations.
Positions
Senior Regulatory Affairs Associate
Clinical Research Associate
Regulatory Affairs Associate (2 positions)
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Senior Regulatory Affairs Associate (#SRA-01)
As the Senior Regulatory Affairs Associate you will be responsible for administration/co-ordination of regulatory/registration activities and task assignments. You will be interacting closely with our internal clinical, marketing and quality control staff along with external contacts and agencies. A thorough understanding of TPP, FDA, European and other international regulations is essential. You should have a minimum of 5-6 years experience in pharmaceutical regulatory affairs, along with a B.Sc. in Chemistry or a health related discipline. Your communication and presentation skills will be actively used in supporting the department's activities and various R&D projects.
Clinical Research Associate (#CRA-01)
As Clinical Research Associate you will be responsible for monitoring and administration of clinical sites, and provide assistance with other clinical and regulatory duties as required. You should have a B.Sc. in a clinically based field or at least 4 years experience in the health science area, excellent computer skills, at least 2 years monitoring experience, and GCP training. Good interpersonal skills are essential. Muti-tasking and organizational skills required.
Regulatory Affairs Associate (#RAA-01)
The successful candidate will be responsible for carrying out registration activities pertaining to Canadian, American, and other International filings. You will be interacting closely with our internal Clinical, Marketing, and Quality Control staff along with external contacts and agencies. A thorough understanding of TPP and FDA regulations is essential. A general knowledge of European and other International regulations would be an asset. You should have a minimum of 3-4 years experience in pharmaceutical Regulatory Affairs along with a B.Sc. or M.Sc. in Chemistry or a health related discipline. Your excellent communication and presentation skills will be actively used in assisting with the coordination of multiple R&D projects.
Regulatory Affairs Associate (#RAA-02)
As Regulatory Affairs Associate you will be responsible for compiling and generating documentation required for the drug Provincial Formulary Submissions, Canadian, U.S. and international registration, prepare pharmaco-economic analysis of various drug products, provide assistance in the write-up of research protocols, scientific reviews and technical support on assigned projects. You should have a minimum of a B.Sc. degree or the equivalent in Chemistry, Pharmacy of Life Sciences, 3-5 years experience in a QA/QC or Regulatory environment, familiarity with pharmaceuticals, GMP and regulatory requirements. Your excellent communication, presentation and organizational skills and ability to work in a team environment are mandatory.
Fax your resume in confidence to:
Human Resources
DIMETHAID RESEARCH INC.
1405 Denison Street
Markham, Ontario
L3R 5V2
FAX: (905) 415-1440
or e-mail: ccarter@dimethaid.com
No telephone inquiries please. Only those selected for interview will be contacted.
We offer industry competitive salaries and benefits, and an excellent working environment. |
