Clinical Programer (m/f/d) remote/office-based/hybrid
at GCPService International
Bremen, Bremen, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 21 Dec, 2024 | Not Specified | 22 Sep, 2024 | N/A | Specifications,Figures,Sas,Timelines | 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:
You love programming in SAS and would like to use your skills in a dynamic, international team working on bringing new treatments to patients? Then you should consider joining us! We are expanding our team and are looking for a dynamic full-time Clinical Programmer who wants to join our motivated group of Clinical Programmers and Biostatisticians. While the statistics department is centered in our headquarter in Bremen, we are open to have someone join us full-time or hybrid in any of our offices (Bremen, Siegburg, Berlin, Prague) or in a home-based position. We are looking for someone who is open to taking responsibility for projects and supporting our team of statisticians with trial evaluations. Your tasks ranges from review of the database setup to improve final evaluation, to programming of tables, figures and listings based on specifications provided by the team of statisticians. First experience with data conversions into CDISC SDTM& ADaM format is a strong plus. In this context, we are looking for a candidate who understands the importance of the following:
- Taking responsibility for the communication with your colleagues regarding all programming-related questions within a project
- Having organizational skills to adhere to timelines, and of completing projects early enough to reduce turn-around time after the final data is available
Being able to think outside the box and finding creative solutions to standardization of programming tasks
Your profile:
Excellent command of SAS®
- Initial experience as (SAS) Programmer a plus
- Good communication and self-management skills
- Basic understanding of regulatory requirements of clinical trials
- Great spoken and writing English (German is a plus)
Knowledge of CDISC SDTM & ADaM, or willingness to delve into it, a strong plus
We offer:
An independent, diverse and interesting area of responsibilities and an excellent working environment
- A young and innovative corporate culture and management, with a clear path to personal development and the opportunity to take responsibility not only within projects, but also within the company
- Support and advancement in individual personal and professional development
- Modern and performance-oriented remuneration systems
- Flexible working hours
- Flexible working environment (office-based, hybrid, home-based)
If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date:
Andreas Beust (Chief Executive Officer)
GCP-Service International Ltd. & Co.KG
Anne-Conway-Str. 2
28359 Bremen Germany
Phone: +49 (0)421 20 80 98 51
E-mail: application@gcp-service.co
Responsibilities:
- Taking responsibility for the communication with your colleagues regarding all programming-related questions within a project
- Having organizational skills to adhere to timelines, and of completing projects early enough to reduce turn-around time after the final data is available
- Being able to think outside the box and finding creative solutions to standardization of programming task
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
Proficient
1
Bremen, Germany