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Senior Drug Safety Physician
- Posted 19 October 2022
- LocationAllschwil
- Job type Permanent
- Reference70658
- Contact NameDominic Pritchard
Job description
Senior Drug Safety Physician (Director Level)
Offer
- Permanent position
- Onsite Basel location
- Hybrid working - min 3 days per week on site (4 days per week for those commuting across boarders)
- Stand alone position (no direct reports) in a team of 4 other Drug Safety Physicians
- Relocation package available for those relocating to Switzerland
Responsibilities:
- Medical assessment, aggregate report writing, signal detection, risk management, risk minimalization
- Integration, analysis and interpretation of safety information
- Working to GCP and GVP
- Regulatory filing, safety documents (DSUR, PBRER, RMP, CCDs),
- Use of Argus database for review of SAE and post marketing
- amongst other responsibilities
Requirements
- Medical Doctor with 10+ global drug safety experience in clinical and post-marketing safety (experience in clinical filing would be a nice to have)
- Good clinical development knowledge and data interpretation expertise.
Fluent English
- Good presentation and confidence to discuss results/proposals etc with senior management, project teams, drug safety committee etc
If this role is for then please reach out to Dom on +41415625046, dominic.pritchard@biotalent.com to discuss OR if you know someone who this will be suited to then please put us in touch.
Offer
- Permanent position
- Onsite Basel location
- Hybrid working - min 3 days per week on site (4 days per week for those commuting across boarders)
- Stand alone position (no direct reports) in a team of 4 other Drug Safety Physicians
- Relocation package available for those relocating to Switzerland
Responsibilities:
- Medical assessment, aggregate report writing, signal detection, risk management, risk minimalization
- Integration, analysis and interpretation of safety information
- Working to GCP and GVP
- Regulatory filing, safety documents (DSUR, PBRER, RMP, CCDs),
- Use of Argus database for review of SAE and post marketing
- amongst other responsibilities
Requirements
- Medical Doctor with 10+ global drug safety experience in clinical and post-marketing safety (experience in clinical filing would be a nice to have)
- Good clinical development knowledge and data interpretation expertise.
Fluent English
- Good presentation and confidence to discuss results/proposals etc with senior management, project teams, drug safety committee etc
If this role is for then please reach out to Dom on +41415625046, dominic.pritchard@biotalent.com to discuss OR if you know someone who this will be suited to then please put us in touch.