Clinical Programming Manager (gn)
Clinical Programming Manager (gn)
Clinical Programming Manager (gn)
Clinical Programming Manager (gn)
MANPOWER GmbH & Co. KG
Personaldienstleistungen und -beratung
Ulm
- Art der Anstellung: Vollzeit
- 59.500 € – 82.500 € (von XING geschätzt)
- Remote
Clinical Programming Manager (gn)
Über diesen Job
Your application for the position of Clinical Programming Manager (all genders) is in good hands Find the right job with Manpower! As specialists in the industrial sector with 46 locations nationwide, we have the experience to make the most of your skills.
What we offer you:
- Holiday and Christmas bonus
- Numerous employee discounts
- Free advice and job placement
- Tailored role matching
- Personal support and professional profile creation
- Interview coaching and preparation
- Get to know exciting companies in your region
- 100% remote
Your Responsibilities:
- Provide input to budget planning.
- Oversee contingent workers and/or vendors; provide training to others as needed.
- Operate primarily at project level, coordinating deliverables across functions.
- Deliver assignments with high quality and within agreed timelines.
- Contribute to programming strategy under moderate supervision.
- Provide strong programming support for CDISC-based e-submissions
- : develop, review, and/or validate generic macros; develop, debug, and enhance SAS
- programs to support QC of safety/efficacy derived datasets.
- Apply solid understanding of statistical models used in efficacy analyses.
- Standardize Clinical Programming deliverables within the project.
- Extend existing or develop new clinical-programming methods to solve complex problems.
Qualifications:
- Bachelors/Masters/PhD in Science, Statistics, Information Technology, or a related field; or equivalent combination of education and relevant work experience.
- Bachelors + 5 years or Masters + 4 years of programming experience in a pharmaceutical or clinical research setting.
- Preferred: Hands-on experience with SDTM and ADaM and familiarity with CDISC
- guidelines and requirements.
- Advanced SAS programming; ability to develop SAS programs and perform QC for integrated analyses.
- Experience developing/validating macros; strong debugging and enhancement skills for submission-grade code.
- Intermediate knowledge of government regulations relevant to drug development across multiple therapeutic areas.
- Contributes to strategy under moderate supervision.
- Tackles difficult problems; identifies solutions and recommends actions to management.
- Influences communication toward common understanding and actionable results; contributes to process development.
- Effective in global, cross-functional environments.
- Able to collaborate and influence without direct reporting lines.
Have we convinced you? Then apply now! We look forward to receiving your application via the Apply button or using the contact details provided. Cant meet every single requirement? That shouldnt stop you from applying. Above all, we value enthusiasm and a willingness to learn and work across different disciplines. We embrace diversity and equal opportunity and therefore welcome applications from people with disabilities. All personal terms used in this job posting are intended to be gender-neutral.
Bereitgestellt in Kooperation mit der Bundesagentur für Arbeit.