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| Reference: |
2804 |
| Date Posted: |
4/21/2008 |
| Organization: |
Sterling-Hoffman Life Sciences |
| Employment Type: |
Full Time |
| Location: |
Thornhill, Ontario |
Description:
Our client is a global pharmaceutical company headquartered in Thornhill that is focused on the development and manufacturing of various dermatology therapeutics. The company has marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate!
Job Responsibilities:
1) Manage assigned projects by carrying out all the functions of Principle Clinical Project Coordination (PCPC) or Local Clinical Project Coordination (LCPC) as defined in standard operating procedures (SOPs)
2) Contribute to the quality of research that results in optimal healthcare outcomes from company’s products and services by ensuring the successful outcome of each clinical trial
3) Study background material and keep abreast of trends related to area of tasks
4) Draft protocols for approval of proposed clinical trials
5) Plan and complete assigned projects as per projected timelines and budgets
6) Assist with training of Clinical Research Associates
7) Determine investigators’ participation in the trial(s)
8) Provide investigators and cites with information to ensure that trials are conducted as per ICH Guidelines and SOPs
9) Consult investigators on trial or for reporting serious and/or unexpected adverse events
10) Ensure that the staff assigned to projects conducts them as per GCPs and SOPs, including site monitoring, drug accountability, adverse event reporting, data validation, data handling, report production, filing and archiving
11) Participate in product development with the strategy teams
12) Provide feedback (on an ongoing basis) to team members
13) Perform other assignments (as required)
Job Requirements:
1) MD or Ph. D.
2) 1-year clinical project management experience or 1 – 2 years of related clinical experience
3) Thorough knowledge of Good Clinical Practices
4) Work well in a team environment and independently
5) Ability to work competently in Windows Office and with Project Management
6) Ability and willingness to travel
Applicants are encouraged to apply directly by going to: http://www.sterlinglifesciences.com/jobs/lifesciences-jobs-02804.html
Salary: $80k-$85k
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| Healthcare Field: |
Biotechnology |
| Category: |
Clinical Research Associate |
| SubCategory: |
None |
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Job Posted By:
Similee Harvey
Sterling-Hoffman Life Sciences
800 West El Camino Real ,Suite 180
Mountain View
United States
94040
View more jobs posted by Similee Harvey |