Sterling-Hoffman Executive Search
Home
Our Story
Domain Expertise
Clients
Career Opportunities
Community
Contact Us
Submit your resume
Interviewing Guidelines








    
Sign-up
for the Sterling-Hoffman Life Sciences Journal to get the latest industry news and job postings.
Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
Career Opportunities
Back

To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

 Job #02795 Email this job to a friend
About our client
Our client is a publicly traded company. The company has an experienced management team, a robust pipeline, and an empowering corporate culture that is focused on the professional development of its employees.
Position Location
Research Scientist III (Bioanalytical Chemistry) Western Canada
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Design and manage the bioanalytical support of investigative ADME, pre-clinical, and clinical pharmacokinetic studies
2) Develop and validate HPLC/UV as well as LC/MS/MS assays for analysis of pre-clinical and clinical biological samples
3) Participate in troubleshooting bioanalytical procedures
4) Identify and characterize new chemical entities and metabolites
5) Oversee data analysis, interpretation, and computer modeling
6) Manage in-house bioanalysis, supporting non-clinical and clinical studies
7) Generate, maintain, and implement study protocols and SOPs
8) Develop and troubleshoot analytical methods
9) Review data, perform statistical analyses, and handle report generation
10) Supervise, train, and ensure professional development of junior researchers
11) Prepare manuscripts for publication in professional journals as well as materials for meetings and conferences
12) Keep abreast of current technology, principles, and theories
13) Manage CROs and projects
14) Work as a Technical Lead for all outsourced bioanalytical studies
15) Anticipate and troubleshoot the potential scientific and logistic problems
16) Conduct site audits
17) Evaluate and initiate outsourcing collaborations and contract negotiation
18) Manage external project budget
19) Develop and implement CRO management plans to ensure timely achievement of project objectives in support of pre-clinical and clinical studies, with adherence to budget and GLP compliance
20) Review data and reports for externally contracted projects
21) Communicate and provide progress updates on external study activities to Internal Program/Project Team
22) Provide technical support as well as manage bioanalytical studies at CROs
23) Prepare technical reports and supporting documentation
24) Perform other relevant duties as assigned
Requirements
1) Ph. D. in Chemistry or Bioanalytical Chemistry
2) Demonstrated experience in managing a bioanalytical laboratory
3) Experience in a GLP environment preferred
4) Experience in selecting and managing outside contractors for bioanalysis in support of clinical and toxicology studies
5) Excellent project-management skills

Back
Home | Our Story | Domain Expertise | Clients | Career Opportunities | Community | Contact Us