Associate Director
- Recruiter
- Achieva Group Ltd
- Location
-
Hertfordshire
East of EnglandUnited Kingdom
- Salary
- Competitive
- Posted
- 10 Apr 2021
- Closes
- 11 Apr 2021
- Job Title
- Associate Director
- Category
- Scientific and Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
*Our global pharmaceutical client has a vacancy for an Associate Director – Pharmacovigilance.*
Our client is looking for candidates based in UK.
This is an initial 12–month full time contract.
*Job Responsibilities: *
??? Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas
??? Responsible for individual and aggregate case reporting activities including ICSR case management (medical review) and aggregate reporting (i.e. DSUR, PBRER)
??? Responsible for signal detection and management activities including, but not limited to STAR maintenance, ISMP maintenance. Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests
*Education, Skills and Experience *
Minimum Qualifications: Qualified healthcare professional or Life Sciences graduate.
Preferred Qualifications: A relevant postgraduate qualification (e.g. PHD/MSc in a Life sciences discipline; Medical qualification; PharmD or other post–graduate health professional qualifications) would be advantageous
Safety scientist (level 2): 2 or more years of drug safety, clinical development or medical affairs experience in the pharmaceutical or related industry
??? Understanding of GxP and regulated processes and end to end clinical trial lifecycle
??? Strong orientation towards process improvement and cross–functional teamwork
??? Effectively work with remote partners on a global team
??? Excellent communication skills, both written and verbal
??? Perform data analysis / statistical methods to evaluate, interpret and present scientific data with clarity
??? Good presentation skills, effective at summarizing and presenting the key considerations and decision points
??? Ability to train others on departmental practices and processes
??? Understanding of project management methodology
Our client is looking for candidates based in UK.
This is an initial 12–month full time contract.
*Job Responsibilities: *
??? Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas
??? Responsible for individual and aggregate case reporting activities including ICSR case management (medical review) and aggregate reporting (i.e. DSUR, PBRER)
??? Responsible for signal detection and management activities including, but not limited to STAR maintenance, ISMP maintenance. Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests
*Education, Skills and Experience *
Minimum Qualifications: Qualified healthcare professional or Life Sciences graduate.
Preferred Qualifications: A relevant postgraduate qualification (e.g. PHD/MSc in a Life sciences discipline; Medical qualification; PharmD or other post–graduate health professional qualifications) would be advantageous
Safety scientist (level 2): 2 or more years of drug safety, clinical development or medical affairs experience in the pharmaceutical or related industry
??? Understanding of GxP and regulated processes and end to end clinical trial lifecycle
??? Strong orientation towards process improvement and cross–functional teamwork
??? Effectively work with remote partners on a global team
??? Excellent communication skills, both written and verbal
??? Perform data analysis / statistical methods to evaluate, interpret and present scientific data with clarity
??? Good presentation skills, effective at summarizing and presenting the key considerations and decision points
??? Ability to train others on departmental practices and processes
??? Understanding of project management methodology
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