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R&D Domain Expert - SAS
Eingestellt von Elevate Direct
Gesuchte Skills: Support
Projektbeschreibung
R&D DOMAIN EXPERT/BEERSE, BELGIUM/6 MONTHS CONTRACT/UP TO 79 EUR PER HR
This position is part of the data processing solutions team, which focuses on the central data platforms for clinical studies. This platform is built upon and around SAS Drug Development (SDD) to deliver the user community (data managers of clinical studies) with an integrated process for study data processing, analysis and validation.
The candidate will be part of the team and deliver platform expertise, mainly based around SAS development activities and process improvements.
RESPONSIBILITIES
Work independently on SAS programs to support our services: developing, reviewing and testing programs to deliver clinical study reviews and QC
Works on medium complexity projects. Ensures quality project deliverables as agreed upon with internal and external customers.
Defines and develops maintenance or enhancements in multiple areas of domain expertise.
Shares multiple domain expertise with IDAR Operations and CRO's to assure consistency and accuracy within process and functionality.
Assist in improving/developing departmental processes, SOPs and documentation
Provide programming training, presentations and support to colleagues
Participates in process, system, and tool improvement initiatives within IDAR business groups.
Participates in non-trials/non-program projects to gather information or provide guidance in multiple domain expertise areas.
Support audit and inspections as appropriate.
The services will be performed within the framework of GXP guidelines like system validation
EDUCATION/EXPERIENCE
Minimal Bachelor degree in statistics, computer science or related
Proven experience with SAS in a clinical study environment
Proven knowledge of SDTM & ADAM standards
SAS drug development knowledge would be a plus
Knowledge and/or experience with Pharma R&D, and clinical studies in particular is required
Good understanding and experience with systems development processes
QUALIFICATIONS/COMPETENCIES
Team work experience
Project management skills
Internal
- Quick learner, motivated self-starter;
- Excellent customer service, interpersonal, communication and team collaboration skills;
- Able to follow change management for internal guidelines.
LANGUAGE PROFICIENCIES:
-English and Dutch spoken and written;
THE COMPANY
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.
This position is part of the data processing solutions team, which focuses on the central data platforms for clinical studies. This platform is built upon and around SAS Drug Development (SDD) to deliver the user community (data managers of clinical studies) with an integrated process for study data processing, analysis and validation.
The candidate will be part of the team and deliver platform expertise, mainly based around SAS development activities and process improvements.
RESPONSIBILITIES
Work independently on SAS programs to support our services: developing, reviewing and testing programs to deliver clinical study reviews and QC
Works on medium complexity projects. Ensures quality project deliverables as agreed upon with internal and external customers.
Defines and develops maintenance or enhancements in multiple areas of domain expertise.
Shares multiple domain expertise with IDAR Operations and CRO's to assure consistency and accuracy within process and functionality.
Assist in improving/developing departmental processes, SOPs and documentation
Provide programming training, presentations and support to colleagues
Participates in process, system, and tool improvement initiatives within IDAR business groups.
Participates in non-trials/non-program projects to gather information or provide guidance in multiple domain expertise areas.
Support audit and inspections as appropriate.
The services will be performed within the framework of GXP guidelines like system validation
EDUCATION/EXPERIENCE
Minimal Bachelor degree in statistics, computer science or related
Proven experience with SAS in a clinical study environment
Proven knowledge of SDTM & ADAM standards
SAS drug development knowledge would be a plus
Knowledge and/or experience with Pharma R&D, and clinical studies in particular is required
Good understanding and experience with systems development processes
QUALIFICATIONS/COMPETENCIES
Team work experience
Project management skills
Internal
- Quick learner, motivated self-starter;
- Excellent customer service, interpersonal, communication and team collaboration skills;
- Able to follow change management for internal guidelines.
LANGUAGE PROFICIENCIES:
-English and Dutch spoken and written;
THE COMPANY
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges