PLEASE RESPOND TO anil@trustek.com OR CALL 732-393-1313 EXT 106
Location: NJ
Duration: 6+ Months
Scope of expected activities are:
Specifications development and maintenance
Derived data set development and validation
Output (TFL) programming development and validation
Data pooling
CDISC data set definitions work
Coordinated and work assignments managed by client Project Leads and Lead Programmers
Will work directly on clients systems via external laptop or company laptop
Clients processes will be followed and training and onboarding will be provided
Experience/Professional requirement:
1. Advanced knowledge of / experience with SAS and other relevant programming software.
2. Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills
3. Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent)
4. Working knowledge of database design/structures and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or
equivalent)
5. Good understanding of global clinical trial / project practices, procedures, methodologies.
6. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).
7. Intermediate knowledge of office tools.
8. At least 5 years work experience in a programming role preferably supporting clinical trials
Thanks and Regards,
Anil K
TRUSTEK INC |
1001 Durham Ave, Suite # 306, South Plainfield, NJ 07080|
Work: 732-393-1313 Ext 106|| Fax: (866)-294-1314|
anil@trustek.com| YIM: anil.trustek| 
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