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Senior Statistical Programmer
Ref No.: 18-08157
Location: Cambridge, Massachusetts
Req#: 8132904
Type: Staffing
Status: Pending
Client: Alnylam
Start: 05/22/2018
End: 05/21/2019

Description:
Status: Pending
Status Reason: Pending Sourcing

Reason: New Contingent Hire
Department: Data Sciences and Statistics Job Category: Data Sciences & Statistics Job Code: Senior Statistical Programmer Job Title: Senior Statistical Programmer
Duties:



We are seeking an experienced statistical programmer consultant who will primarily work on safety ADaM datasets and TLFs programming. He/She will develop, maintain, validate and run SAS computer programs that access, visualize, analyze, and report clinical trial data, in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. Candidate should have ability to work independently. The position reports to the Senior Manager of Statistical Programming. Key Responsibilities Write SAS programs that produce tables, listings, figures and analysis datasets; Write SAS programs that validate tables, listings, figures, and analysis datasets; Follow good programming practices, including adequately documenting SAS code; Use, modify, and maintain existing SAS code; Write specifications to describe programming needs; Assist in developing programming processes consistent with industry best practices; Review DMP, eCRF specs, and other clinical data management documents; Review statistical analysis plans and other related documents; Partner with CRO to perform any of the above tasks; Other duties as assigned.

Flexibility: Remote work: 1 day /week
Flexible, Onsite log in / log off hours, provided logs alteast 8 hours per day
with 5 hour overlap with the core team.





Skills:


At least 5 years industry (Pharmaceutical, Biotech, CRO) SAS programming experience or equivalent; Knowledge of clinical trials and experience in using SAS Enterprise Guide or SAS Studio to report the results of clinical trials; Experience in producing validated SAS programs; Experience in working with CDISC standards, including SDTM, and ADaM; Excellent knowledge of applied statistical methodologies; Excellent knowledge of SAS Macro, SAS/SQL, SAS/GRAPH, and SAS/STAT; Good communications skills required; Clear alignment with Alnylam Core Values: • Commitment to People • Innovation and Discovery • Sense of Urgency • Open Culture • Passion for Excellence




Keywords:
Education:


Bachelor's Degree required, Master's Degree Preferred.



Skills and Experience:
Required Skills:
CLINICAL DATA MANAGEMENT
CLINICAL TRIALS
CRO
DATA MANAGEMENT
DATASETS
Additional Skills:
DOCUMENTING
SAS
SQL
STATISTICAL ANALYSIS
STATISTICAL PROGRAMMING
CLINICAL TRIAL
ICH
SERIAL ATTACHED SCSI
Languages:
English
Read
Write
Speak
Minimum Degree Required: Bachelor's Degree
Patents: No
Publications: No
Veteran Status: No
# of Positions: 1

Location:
Cambridge, MA
101 Main Street,

Schedule:
Start Date: 05/22/2018
Estimated End Date: 05/21/2019
Hours Per Week: 40.00
Hours Per Day: 8.00
Standard Schedule:
Schedule Notes: Flexible work schedule