Data operations manager állás, munka

The independent analyses of secondary data, including insurance claims, electronic medical record, patient survey, and disease registry....

PHARMACOEPIDEMIOLOGIST (M/F/D)- RWD/ EPIDEMIOLOGICAL/ PHARMACOEPIDEMIOLOGIC/ CLINICAL TRAILS/ BIOMARKER/ INSURANCE CLAIMS/ EHR/ MEDICAL/ MEDDRA/ SNOMED/ ICD 10/ CPT/ HCPCS/ R/ PYTHON/ SQL/ DATA VISUALIZATIONS/ R SHINY/ R MARKDOWM/ STATISTICAL ANALYSIS/ ENGLISH PROJECT: For our customer a big...

• Start Date: asap
• Latest Start: February 2026
• Planned Duration: 9-month maternity cover
• Extension: possible
• Location: Basel
• Workload: 100%
• Home Office: 2 days/week after 2-3 months onboarding
• Travel: none
• Team Size: 6 people
• Template Used: CH_Real World Data Scientist_LSW_CHF_RCM_CO

PHARMACOEPIDEMIOLOGIST (M/F/D)- RWD/ EPIDEMIOLOGICAL/ PHARMACOEPIDEMIOLOGIC/ CLINICAL TRAILS/ BIOMARKER/ INSURANCE CLAIMS/ EHR/ MEDICAL/ MEDDRA/ SNOMED/ ICD 10/ CPT/ HCPCS/ R/ PYTHON/ SQL/ DATA VISUALIZATIONS/ R SHINY/ R MARKDOWM/ STATISTICAL ANALYSIS/ ENGLISH PROJECT: For our customer a big...

• A degree in Public Health, Epidemiology, Outcomes Research, Health Economics or a related scientific field; MSc or PhD in Epidemiology preferred
• Minimum 2 years of hands-on experience with Real World Data, non-interventional study design and analysis

• Start Date:or
• Latest Possible Start:
• Duration: 6 months initially; extension possible (e.g., additional 6 months)
• Location: Basel
• Workload: 100%
• Home Office: Yes
• Travel: Not expected
• Team Size: PCS safety team approx. 6; cross-functional project teamsmembers
• Hiring Manager: Simone Melega

For our partner located in the canton of Bern, GI Life Sciences is looking for a: SENIOR SCIENTIST BIO-/CHEMICAL QUALITY CONTROL Start : Mid-November End : YOUR MISSION : As a SENIOR SCIENTIST IN BIO-/CHEMICAL QUALITY CONTROL, you will play a key role in establishing the BCQC unit within the...

Framework and Content: Develop and maintain global sales capability frameworks, designing high-impact training content (in partnership with external vendors when necessary) focused on product knowledge, clinical confidence, and compliant HCP engagement in the aesthetic space....

End-to-End Ownership – act as the bridge between development, clinical, testing, and UX, taking responsibility for features from concept to release, ensuring no gaps remain unnoticed, with support from an experienced team....

• Design, develop, and optimize coagulation diagnostic assays and reagents
• Lead feasibility studies, verification, and validation activities in compliance with ISOand IVDR requirements
• Document all activities according to quality system procedures and design control standards

Prepare, support the creation and review and execute the release of all technical documentation for digital health and software products ensuring compliance with applicable standards and regulatory requirements such as IEC, IEC...