Senior Specialist Platform Technologies
at Pharmalex
Hamburg, Hamburg, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 06 Sep, 2024 | Not Specified | 07 Jun, 2024 | 2 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
WE ARE GROWING, GROW WITH US!
Are you eager to work in a dynamic company where new challenges and opportunities are part of your everyday life? Then, PharmaLex is your career choice!
PharmaLex is part of Cencora – the leading service provider for the pharmaceutical, biotech and medical device industries globally. PharmaLex is specialised in effectively designing all aspects of drugs and medical devices regulatory needs, ranging from early development and market entry to product maintenance activities.
We are looking for an additional team member to join remotely our Platform Technologies team.
A great opportunity for a Pharmacovigilance expert who would like to work with internal departments, as well as clients..
YOUR PROFILE
- At least 3 years of experience within the Pharmacovigilance, Safety Reporting, or Clinical Trials area in a pharmaceutical, biotech, or CRO company – and at least 2 years’ experience specifically with clinical trials or (safety) document distribution systems.
- Bachelor of Science in computer or natural science, or a comparable education.
- Strong communicator fluent in English; German beneficial.
- Autonomous, concentrated, and highly organized with strong attention to detail and keen analytical skills – and the ability to efficiently multi-task and handle competing priorities.
- Ability to work enthusiastically and collaboratively as part of a cohesive group and also independently, as needed.
- Proactive approach to ensuring continuous improvement and growth for oneself, the Business Services Team, and the Pharmasol organization.
- Technical experience, such as general knowledge of database structures/models and with writing SQL queries, beneficial.
- Good knowledge of Computerised Software Validation (GAMP 5) and 21 CFR Part 11.
- Project management experience preferable
If you are interested in joining our Pharmalex team taking over this challenging job opportunity in our future-oriented company, we are looking forward to receive your application documents stating your earliest possible starting date, any visa requirements and salary expectations on-line.
For further information please don’t hesitate to contact us.
Agencies only by prior agreement for the specific job opportunity
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:2.0Max:3.0 year(s)
Information Technology/IT
Software Engineering
Graduate
Proficient
1
Hamburg, Germany